Description:Job Summary: To deputize for the QA/RA Director(s) in their absence. To act as a responsible Person as required by regulation. To have direct responsibility for technical files (STED), international registration and to keep the company abreast of new regulations that are applicable. To assist with 510(k) and clinical trials.Quality Assurance responsibilities are risk management, auditing and new product development design control although other duties may be assigned as required.Responsibilities: Sole: Construct and maintain Standard Technical files as evidence of compliance to European and US regulations and other authorities as required.Sole: To produce reports and training literature on new regulations.Sole: To oversee the RoHS technical file construction and to verify their compliance.Sole: To produce post market surveillance reports and trending.Joint: To ensure risk management files are compliant to ISO14971 and are current.Joint: To give strategic direction for 510(k) and clinical trials.joint: As required, to be a contact person for European authorities and FDA.Joint: To take on and manage discrete quality or regulatory projects.Joint: To be involved in and to manage planned site inspections and Audits.Joint: To be the Regulatory subject matter expert for design control projects.Joint: To conduct secondary and third party audits.Joint: To act as one of company's Qualified Person (responsibilities are defined by regulation).Joint: to be a Subject Matter Expert for vigilance and reportable events.Joint: To write procedures in support of Quality, Regulatory and Clinical processes.Joint: To train Dynex personnel on quality and regulatory topics.Sole: to act as the Quality Representative for all Dynex European sites.Joint: to assist with shipping compliance issues.Supervisory Responsibilities: Direct report of Regulatory Associate(s). Responsible for project managing discrete projects.Success Factors: To be able to work independently and to manage project teams. To stay up to date with the current regulatory changes. To be able to communicate effectively through both written media and verbally. Strong mediation and negotiation skills. It would be beneficial to have formal qualification in auditing and project management..Requirements:Minimum Qualifications/Education: Specific knowledge of International standards and regulations inclusive of ISO, FDA, and EC/98/79 IVDD. A minimum of 5 years working with IVD devices with a scientific or engineering degree.Computer Skills: Computer literacy in Windows, Word, Excel, Power point and Vision.Work Environment: Office.Physical Requirements: Must be able to meet National Institute for Occupational Safety & Health (NIOSH) Standards.PI107742227
Feb 15, 2019
Description:Job Summary: To deputize for the QA/RA Director(s) in their absence. To act as a responsible Person as required by regulation. To have direct responsibility for technical files (STED), international registration and to keep the company abreast of new regulations that are applicable. To assist with 510(k) and clinical trials.Quality Assurance responsibilities are risk management, auditing and new product development design control although other duties may be assigned as required.Responsibilities: Sole: Construct and maintain Standard Technical files as evidence of compliance to European and US regulations and other authorities as required.Sole: To produce reports and training literature on new regulations.Sole: To oversee the RoHS technical file construction and to verify their compliance.Sole: To produce post market surveillance reports and trending.Joint: To ensure risk management files are compliant to ISO14971 and are current.Joint: To give strategic direction for 510(k) and clinical trials.joint: As required, to be a contact person for European authorities and FDA.Joint: To take on and manage discrete quality or regulatory projects.Joint: To be involved in and to manage planned site inspections and Audits.Joint: To be the Regulatory subject matter expert for design control projects.Joint: To conduct secondary and third party audits.Joint: To act as one of company's Qualified Person (responsibilities are defined by regulation).Joint: to be a Subject Matter Expert for vigilance and reportable events.Joint: To write procedures in support of Quality, Regulatory and Clinical processes.Joint: To train Dynex personnel on quality and regulatory topics.Sole: to act as the Quality Representative for all Dynex European sites.Joint: to assist with shipping compliance issues.Supervisory Responsibilities: Direct report of Regulatory Associate(s). Responsible for project managing discrete projects.Success Factors: To be able to work independently and to manage project teams. To stay up to date with the current regulatory changes. To be able to communicate effectively through both written media and verbally. Strong mediation and negotiation skills. It would be beneficial to have formal qualification in auditing and project management..Requirements:Minimum Qualifications/Education: Specific knowledge of International standards and regulations inclusive of ISO, FDA, and EC/98/79 IVDD. A minimum of 5 years working with IVD devices with a scientific or engineering degree.Computer Skills: Computer literacy in Windows, Word, Excel, Power point and Vision.Work Environment: Office.Physical Requirements: Must be able to meet National Institute for Occupational Safety & Health (NIOSH) Standards.PI107742227
Description:Summary: Improve the manufacturability and quality in production including both product design and manufacturing issues. Assist in the manufacturing support for all electronics based assemblies. Provide quick response to technical issues on the manufacturing floor and occasionally in the field. Facilitate the introduction of new product designs from R&D into manufacturing. Update design of PCBs to keep them using current technology.Responsibilities: Investigate Engineering Investigation Requests and implement Engineering Change Orders. Troubleshoot circuit board assemblies and implement design improvements. Make changes as necessary due to component obsolescence. Utilize electronics CAD software to create new designs and upgrade existing products. Provide technical expertise to manufacturing and other departments. Initiate, implement, and upgrade assembly and test procedures protocols for electro-mechanical instruments. Perform root cause analysis and assist with the repair of systems and components returned from the field. Troubleshoot electro-mechanical assemblies and recommend design improvements. Coordinate test script, firmware, and software upgrades with Software personnel. Train manufacturing personnel on manufacturing procedures and assembly methods. Travel to customer sites for analysis of unique product failures. Perform other work related duties as assigned. Supervisory Responsibilities: None.Requirements:Minimum Qualifications: Minimum Bachelors degree in Electrical Engineering or related field.Desired Qualifications: Three years experience with schematic design and PCB layout is required. Experience in a Manufacturing or development environment. Experience spanning electrical, mechanical, and software engineering disciplines. Ability to troubleshoot complex electronic faults to component level. Ability to read and understand mechanical drawings. . Experience with Lean Manufacturing and Six Sigma concepts. Experience with MRP and/or ERP systems. Experience with complex robotic systems.Computer Skills: Proficiency with Altium (or similar) ECAD Software. Proficiency with Windows based software applications.Work Environment: Production.Physical Requirements: Must be able to meet National Institute for Occupational Safety & Health (NIOSH) Standards.PI107742216
Feb 15, 2019
Description:Summary: Improve the manufacturability and quality in production including both product design and manufacturing issues. Assist in the manufacturing support for all electronics based assemblies. Provide quick response to technical issues on the manufacturing floor and occasionally in the field. Facilitate the introduction of new product designs from R&D into manufacturing. Update design of PCBs to keep them using current technology.Responsibilities: Investigate Engineering Investigation Requests and implement Engineering Change Orders. Troubleshoot circuit board assemblies and implement design improvements. Make changes as necessary due to component obsolescence. Utilize electronics CAD software to create new designs and upgrade existing products. Provide technical expertise to manufacturing and other departments. Initiate, implement, and upgrade assembly and test procedures protocols for electro-mechanical instruments. Perform root cause analysis and assist with the repair of systems and components returned from the field. Troubleshoot electro-mechanical assemblies and recommend design improvements. Coordinate test script, firmware, and software upgrades with Software personnel. Train manufacturing personnel on manufacturing procedures and assembly methods. Travel to customer sites for analysis of unique product failures. Perform other work related duties as assigned. Supervisory Responsibilities: None.Requirements:Minimum Qualifications: Minimum Bachelors degree in Electrical Engineering or related field.Desired Qualifications: Three years experience with schematic design and PCB layout is required. Experience in a Manufacturing or development environment. Experience spanning electrical, mechanical, and software engineering disciplines. Ability to troubleshoot complex electronic faults to component level. Ability to read and understand mechanical drawings. . Experience with Lean Manufacturing and Six Sigma concepts. Experience with MRP and/or ERP systems. Experience with complex robotic systems.Computer Skills: Proficiency with Altium (or similar) ECAD Software. Proficiency with Windows based software applications.Work Environment: Production.Physical Requirements: Must be able to meet National Institute for Occupational Safety & Health (NIOSH) Standards.PI107742216
Description:Summary: The Quality Engineer ensures that quality standards are met in accordance with a written quality control and assurance program, standard operating procedures and work instructions. He/she works on semi-routine tasks where ability to recognize deviation from standard practice is required. Responsibilities: Inspects purchased parts, assemblies, accessories, and materials for conformance to specifications, using precision measuring instruments and devices: Examines items for defects in materials, work, and damage occurring in transit. Compares quantity and part number of items received with procurement data and other specifications to ensure completeness and accuracy of order. Inspects and measures items for dimensional accuracy, fit, alignment, and functional operation, according to blueprints (mechanical and electrical schematics), parts manuals, and other specifications, using precision measuring instruments and devices. Approves or rejects items, and records inspection and disposition information. Perform all needed inventory transactions in MRP system. Generates and stores device history documentation. Maintain and control calibration database. Provide engineering recommendation on improving the product and process quality. Develop, review and update quality control and assurance procedures. Perform other duties as required.Supervisory Responsibilities: None..Requirements:Qualifications: Broad knowledge of a discipline involving the use of QA/QC knowledge equivalent to a 2-year college education. Five years of incoming inspection experience.Computer Skills: Able to navigate through MRP system and the network to find purchase orders, vendor information, open, print drawings and specifications. Must be able to run and print reports using the MRP system and Microsoft Office applications.Work Environment: QC Lab/Warehouse.Physical Requirements: Must be able to meet National Institute for Occupational Safety & Health (NIOSH) Standards.PI107742219
Feb 15, 2019
Description:Summary: The Quality Engineer ensures that quality standards are met in accordance with a written quality control and assurance program, standard operating procedures and work instructions. He/she works on semi-routine tasks where ability to recognize deviation from standard practice is required. Responsibilities: Inspects purchased parts, assemblies, accessories, and materials for conformance to specifications, using precision measuring instruments and devices: Examines items for defects in materials, work, and damage occurring in transit. Compares quantity and part number of items received with procurement data and other specifications to ensure completeness and accuracy of order. Inspects and measures items for dimensional accuracy, fit, alignment, and functional operation, according to blueprints (mechanical and electrical schematics), parts manuals, and other specifications, using precision measuring instruments and devices. Approves or rejects items, and records inspection and disposition information. Perform all needed inventory transactions in MRP system. Generates and stores device history documentation. Maintain and control calibration database. Provide engineering recommendation on improving the product and process quality. Develop, review and update quality control and assurance procedures. Perform other duties as required.Supervisory Responsibilities: None..Requirements:Qualifications: Broad knowledge of a discipline involving the use of QA/QC knowledge equivalent to a 2-year college education. Five years of incoming inspection experience.Computer Skills: Able to navigate through MRP system and the network to find purchase orders, vendor information, open, print drawings and specifications. Must be able to run and print reports using the MRP system and Microsoft Office applications.Work Environment: QC Lab/Warehouse.Physical Requirements: Must be able to meet National Institute for Occupational Safety & Health (NIOSH) Standards.PI107742219
Description:Job Summary: Provide high-level on-site technical service and support to clients/customers; responsible for testing, diagnosing, repairing and documenting services of all Dynex Technologies products at customer site or at factory depot. Essential Functions: Test, diagnose, and repair Dynex products; Effectively communicate with customers so that they are completely satisfied; Provide same day or within 24 hours response to customer phone calls and e-mails within one hour of dispatch and follow up within 24 hours after the service is completed; Effectively communicate with Dispatch and Dynex personnel to report your Daily status, service ETA, completed service call information, problems, opportunities, costs and needs of customers; Thoroughly cleanup work area upon completion of a service repair job; Maintain documentation for all ECN, technical bulletins, versions of hardware, firmware, and software for Dynex products; Complete Service orders and customer survey's on-site and obtain a customer signature for all completed work. Complete service reports within 24 hours of returning from field service visits; Complete expense reports within 1 week after last field service visits for that week; Quote on Billable instrument repairs within 3 days of receipt of a quote request/approval; Complete in-house repairs and on site repair of instruments in the given mean time. Supervisory Responsibilities: None .Requirements:Success Factors: One must have the ability to work independently with little direction or supervision; dependable, self-motivated, highly organized; able to prioritize multiple tasks from multiple sources. Willing to take on and resolve a variety of tasks and document results. Minimum Qualifications / Education: AS degree in electronic technology or equivalent. 3 to 5 years of experience. Must be able to travel 60-99% Computer Skills: Proficient in CRM/service software, Word, Excel, Power Point and Outlook. PI107742215
Feb 15, 2019
Description:Job Summary: Provide high-level on-site technical service and support to clients/customers; responsible for testing, diagnosing, repairing and documenting services of all Dynex Technologies products at customer site or at factory depot. Essential Functions: Test, diagnose, and repair Dynex products; Effectively communicate with customers so that they are completely satisfied; Provide same day or within 24 hours response to customer phone calls and e-mails within one hour of dispatch and follow up within 24 hours after the service is completed; Effectively communicate with Dispatch and Dynex personnel to report your Daily status, service ETA, completed service call information, problems, opportunities, costs and needs of customers; Thoroughly cleanup work area upon completion of a service repair job; Maintain documentation for all ECN, technical bulletins, versions of hardware, firmware, and software for Dynex products; Complete Service orders and customer survey's on-site and obtain a customer signature for all completed work. Complete service reports within 24 hours of returning from field service visits; Complete expense reports within 1 week after last field service visits for that week; Quote on Billable instrument repairs within 3 days of receipt of a quote request/approval; Complete in-house repairs and on site repair of instruments in the given mean time. Supervisory Responsibilities: None .Requirements:Success Factors: One must have the ability to work independently with little direction or supervision; dependable, self-motivated, highly organized; able to prioritize multiple tasks from multiple sources. Willing to take on and resolve a variety of tasks and document results. Minimum Qualifications / Education: AS degree in electronic technology or equivalent. 3 to 5 years of experience. Must be able to travel 60-99% Computer Skills: Proficient in CRM/service software, Word, Excel, Power Point and Outlook. PI107742215
Description:Job Summary: The Marketing Manager (MM) role is responsible for all aspects of the product(s) lifecycle. Dynex is developing and launching next generation patented multiplex technology and automation. The MM will work as part of a small marketing team focused on managing the successful development, launch and subsequent growth of the new product line within Dynex. Essential Functions: •Marketing Plans (Strategic look at the market and product)•Launch Plans (Tactical look at execution and launch of product)•Forecasting and Financial Analysis of product line•Analytical business case modeling•CPT codes and global reimbursement analysis•Budgeting?Development & Implementation of Marketing Promotions / Programs/ Sales Tools?Market Research and Analysis?Leading cross-functional team meetings?Voice of customer advocate?Competitive Intelligence?Branding?Lead Generation campaigns?Social Media?Tradeshow organizationSupervisory Responsibilities: No.Requirements:Success Factors: Proactive and self-directed with the ability to tap into both their analytical and creative sides to bring new ideas to the table and to take ownership of assigned products. Able to make data driven and strategic recommendations based on experience and vision and develop business and marketing plans to address customer needs that drive increased market share and profitability.Proficient in a variety of communication skills and can interact directly with senior leadership and internal and external customers.•Self-starter who can identify, create and lead product line•In-depth understanding of the healthcare markets Clinical, LDT/RUO, Life Sciences•Uses analytical skills to generate realistic business case models •Uses clearly defined criteria and practical instinct to drive decision making •Leads and motivates cross functional teams •Innate curiosity to identify new opportunities and approaches •Identifies key customer issues, seeks deep customer understanding•Ability to travel ~ 20%•Results driven with strong work ethic, ambition and drive to succeedMinimum Qualifications / Education: Bachelors degree or higher. Masters preferred. Five to 10 years of relevant healthcare marketing experience with a focus on Clinical Diagnostics or Life Sciences is required. Computer Skills: Proficient in MS Office. Work Environment: Office & Laboratory EnvironmentPhysical Requirements:Must be able to meet National Institute for Occupational Safety & Health (NIOSH) Standards.PI107742212
Feb 15, 2019
Description:Job Summary: The Marketing Manager (MM) role is responsible for all aspects of the product(s) lifecycle. Dynex is developing and launching next generation patented multiplex technology and automation. The MM will work as part of a small marketing team focused on managing the successful development, launch and subsequent growth of the new product line within Dynex. Essential Functions: •Marketing Plans (Strategic look at the market and product)•Launch Plans (Tactical look at execution and launch of product)•Forecasting and Financial Analysis of product line•Analytical business case modeling•CPT codes and global reimbursement analysis•Budgeting?Development & Implementation of Marketing Promotions / Programs/ Sales Tools?Market Research and Analysis?Leading cross-functional team meetings?Voice of customer advocate?Competitive Intelligence?Branding?Lead Generation campaigns?Social Media?Tradeshow organizationSupervisory Responsibilities: No.Requirements:Success Factors: Proactive and self-directed with the ability to tap into both their analytical and creative sides to bring new ideas to the table and to take ownership of assigned products. Able to make data driven and strategic recommendations based on experience and vision and develop business and marketing plans to address customer needs that drive increased market share and profitability.Proficient in a variety of communication skills and can interact directly with senior leadership and internal and external customers.•Self-starter who can identify, create and lead product line•In-depth understanding of the healthcare markets Clinical, LDT/RUO, Life Sciences•Uses analytical skills to generate realistic business case models •Uses clearly defined criteria and practical instinct to drive decision making •Leads and motivates cross functional teams •Innate curiosity to identify new opportunities and approaches •Identifies key customer issues, seeks deep customer understanding•Ability to travel ~ 20%•Results driven with strong work ethic, ambition and drive to succeedMinimum Qualifications / Education: Bachelors degree or higher. Masters preferred. Five to 10 years of relevant healthcare marketing experience with a focus on Clinical Diagnostics or Life Sciences is required. Computer Skills: Proficient in MS Office. Work Environment: Office & Laboratory EnvironmentPhysical Requirements:Must be able to meet National Institute for Occupational Safety & Health (NIOSH) Standards.PI107742212
University of KentuckyEqual Employment Opportunity/M/F/disability/protected veteran status.Posting Details Posting Details Job Title GIS Analyst Requisition Number RE17234 Working Title GIS Analyst Department Name 8H060:Kentucky Transportation Center Work Location 176 Raymond, Lexington Grade Level 44 Salary Range $19.65-31.44/hour Type of Position Staff Position Time Status Full-Time Required Education BS Click here for more information about equivalencies: http://www.uky.edu/hr/employment/working-uk/equivalencies Required Related Experience 3 yrs Required License/Registration/Certification None. Physical Requirements Some lifting, pushing, or pulling of objects up to 50 lbs., and sitting for long periods of time, Shift Monday - Friday; 8:00 am - 5:00 pm. Job Summary The Traffic and Safety program within the Transportation Center offers a range of capabilities and expertise to accomplish the research and evaluation projects undertaken and this position would support and complement existing personnel and program goals. Responsibilities include performing work in the transportation safety area as required to assist other professionals, and as needed, independently complete research projects; working with other transportation-related disciplines and participate in team projects; using research project management techniques effectively; and understanding client needs and potential policy implications of recommended research solutions.IEBC (Internal Employee Being Considered). Skills / Knowledge / Abilities Knowledge/expertise with Highway Safety Manual, MUTCD, Crash Database, MS Office Suite, and ESRI (GIS). Does this position have supervisory responsibilities? No Preferred Education/Experience Deadline to Apply 02/20/2019 University Community of Inclusion The University of Kentucky is committed to a diverse and inclusive workforce by ensuring all our students, faculty, and staff work in an environment of openness and acceptance. We strive to foster a community where people of all backgrounds, identities, and perspectives can feel secure and welcome. We also value the well-being of each of our employees and are dedicated to creating a healthy place to work, learn and live. In the interest of maintaining a safe and healthy environment for our students, employees, patients and visitors the University of Kentucky is a Tobacco & Drug Free campus. As an Equal Opportunity Employer, we strongly encourage veterans, individuals with disabilities, women, and all minorities to consider our employment opportunities. Any candidate offered a position may be required to pass pre-employment screenings as mandated by University of Kentucky Human Resources. These screenings may include a national background check and/or drug screen. Posting Specific QuestionsRequired fields are indicated with an asterisk (*). * Please select the response that best represents your full years paid, full-time, employment experience in traffic and safety, research, and/or engineering. None More than 0, up through 1 year More than 1 year, up through 3 years More than 3 years, up through 5 years More than 5 years * Describe a situation in which you collaborated with individuals outside of your department to accomplish work objectives. (Open Ended Question) * Describe your experiences with geographic information systems and/or spatial data analysis. (Open Ended Question) * Where did you first see this position advertised other than on UK's online employment system? InsideHigherEd.com HigherEdJobs.com Diverseeducation.com (Diverse Issues in Higher Education) HERCjobs.org (Higher Education Recruitment Consortium) InsightIntoDiversity.com Latinosinhighered.com Indeed.com A Colleague, Friend and/or Family Member None of the Above Applicant Documents Required Documents Resume Cover Letter Optional Documents PI107761598
Feb 15, 2019
University of KentuckyEqual Employment Opportunity/M/F/disability/protected veteran status.Posting Details Posting Details Job Title GIS Analyst Requisition Number RE17234 Working Title GIS Analyst Department Name 8H060:Kentucky Transportation Center Work Location 176 Raymond, Lexington Grade Level 44 Salary Range $19.65-31.44/hour Type of Position Staff Position Time Status Full-Time Required Education BS Click here for more information about equivalencies: http://www.uky.edu/hr/employment/working-uk/equivalencies Required Related Experience 3 yrs Required License/Registration/Certification None. Physical Requirements Some lifting, pushing, or pulling of objects up to 50 lbs., and sitting for long periods of time, Shift Monday - Friday; 8:00 am - 5:00 pm. Job Summary The Traffic and Safety program within the Transportation Center offers a range of capabilities and expertise to accomplish the research and evaluation projects undertaken and this position would support and complement existing personnel and program goals. Responsibilities include performing work in the transportation safety area as required to assist other professionals, and as needed, independently complete research projects; working with other transportation-related disciplines and participate in team projects; using research project management techniques effectively; and understanding client needs and potential policy implications of recommended research solutions.IEBC (Internal Employee Being Considered). Skills / Knowledge / Abilities Knowledge/expertise with Highway Safety Manual, MUTCD, Crash Database, MS Office Suite, and ESRI (GIS). Does this position have supervisory responsibilities? No Preferred Education/Experience Deadline to Apply 02/20/2019 University Community of Inclusion The University of Kentucky is committed to a diverse and inclusive workforce by ensuring all our students, faculty, and staff work in an environment of openness and acceptance. We strive to foster a community where people of all backgrounds, identities, and perspectives can feel secure and welcome. We also value the well-being of each of our employees and are dedicated to creating a healthy place to work, learn and live. In the interest of maintaining a safe and healthy environment for our students, employees, patients and visitors the University of Kentucky is a Tobacco & Drug Free campus. As an Equal Opportunity Employer, we strongly encourage veterans, individuals with disabilities, women, and all minorities to consider our employment opportunities. Any candidate offered a position may be required to pass pre-employment screenings as mandated by University of Kentucky Human Resources. These screenings may include a national background check and/or drug screen. Posting Specific QuestionsRequired fields are indicated with an asterisk (*). * Please select the response that best represents your full years paid, full-time, employment experience in traffic and safety, research, and/or engineering. None More than 0, up through 1 year More than 1 year, up through 3 years More than 3 years, up through 5 years More than 5 years * Describe a situation in which you collaborated with individuals outside of your department to accomplish work objectives. (Open Ended Question) * Describe your experiences with geographic information systems and/or spatial data analysis. (Open Ended Question) * Where did you first see this position advertised other than on UK's online employment system? InsideHigherEd.com HigherEdJobs.com Diverseeducation.com (Diverse Issues in Higher Education) HERCjobs.org (Higher Education Recruitment Consortium) InsightIntoDiversity.com Latinosinhighered.com Indeed.com A Colleague, Friend and/or Family Member None of the Above Applicant Documents Required Documents Resume Cover Letter Optional Documents PI107761598
Integrated DNA TechnologiesID 2018-4445Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 13 hours agoShift/Schedule TWThF 8:30P-7:30A (United States of America)Overview The Synthesis Scientist I synthesizes custom oligonucleotides according to the customer's order. This generally includes synthesis, cleavage, deprotection and QC sampling of the products being made.ResponsibilitiesJob Specific Essential Functions:Synthesizes oligos on various synthesizer platformsCleaves and deprotects oligos utilizing appropriate methodsQuantifies and samples oligos for quality control testsAttaches modifications utilizing various techniques Adheres to safety regulations, lab SOPs, and contamination controlsUses lab equipment including limited maintenance and troubleshooting activities Uses custom software packages to complete tasks and create final product Assesses QC data accurately and makes pass/fail decisions for oligos Handles expensive oligos and reagents Keeps thorough records of specialized processes in the oligo process history Follows documented custom instructions, when applicable Demonstrates behavior consistent with the Integrated DNA Technologies Core Values Performs other duties as assignedPosition Specific Essential Functions:Prepares oligos for final shipment to customer or for further processing in other departments.Performs decontamination programs on liquid handling instruments.
Feb 15, 2019
Integrated DNA TechnologiesID 2018-4445Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 13 hours agoShift/Schedule TWThF 8:30P-7:30A (United States of America)Overview The Synthesis Scientist I synthesizes custom oligonucleotides according to the customer's order. This generally includes synthesis, cleavage, deprotection and QC sampling of the products being made.ResponsibilitiesJob Specific Essential Functions:Synthesizes oligos on various synthesizer platformsCleaves and deprotects oligos utilizing appropriate methodsQuantifies and samples oligos for quality control testsAttaches modifications utilizing various techniques Adheres to safety regulations, lab SOPs, and contamination controlsUses lab equipment including limited maintenance and troubleshooting activities Uses custom software packages to complete tasks and create final product Assesses QC data accurately and makes pass/fail decisions for oligos Handles expensive oligos and reagents Keeps thorough records of specialized processes in the oligo process history Follows documented custom instructions, when applicable Demonstrates behavior consistent with the Integrated DNA Technologies Core Values Performs other duties as assignedPosition Specific Essential Functions:Prepares oligos for final shipment to customer or for further processing in other departments.Performs decontamination programs on liquid handling instruments.
Integrated DNA TechnologiesID 2018-4324Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 11 hours agoShift/Schedule MTWThF 3:00P-12:00A (United States of America)Overview The Quality Control Analyst I ensures the quality of processes and products in support of all manufacturing areas within Integrated DNA Technologies. ResponsibilitiesDepartment Functions:Determines pass/fail status of oligos by reviewing analytical data (Mass Spec, CE, HPLC)Disinfects plates and mat caps for re-use by synthesis groupsDisposes of waste in proper mannerEssential Functions:Analyzes data and information for quality, consistency, and accuracyUses a variety of analytical and sample handling equipmentMaintains accurate and detailed sample, product and instrument recordsContributes to and supports an efficient manufacturing environmentComplies with the requirements for an ISO 9001 and ISO 14001 environmentUnderstands and performs necessary emergency, safety and cleaning proceduresHandles sample and reagent preparations (carefully and accurately) for analytical and functional assaysDemonstrates behavior consistent with the Integrated DNA Technologies Core ValuesPerforms other duties as assigned
Feb 14, 2019
Integrated DNA TechnologiesID 2018-4324Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 11 hours agoShift/Schedule MTWThF 3:00P-12:00A (United States of America)Overview The Quality Control Analyst I ensures the quality of processes and products in support of all manufacturing areas within Integrated DNA Technologies. ResponsibilitiesDepartment Functions:Determines pass/fail status of oligos by reviewing analytical data (Mass Spec, CE, HPLC)Disinfects plates and mat caps for re-use by synthesis groupsDisposes of waste in proper mannerEssential Functions:Analyzes data and information for quality, consistency, and accuracyUses a variety of analytical and sample handling equipmentMaintains accurate and detailed sample, product and instrument recordsContributes to and supports an efficient manufacturing environmentComplies with the requirements for an ISO 9001 and ISO 14001 environmentUnderstands and performs necessary emergency, safety and cleaning proceduresHandles sample and reagent preparations (carefully and accurately) for analytical and functional assaysDemonstrates behavior consistent with the Integrated DNA Technologies Core ValuesPerforms other duties as assigned
FluidigmR&D Molecular Biology InternReq No.: 2019-2884Job Location: US-CA-South San FranciscoCategory: Research & DevelopmentType: InternWe are an AA/EEO/Veterans/Disabled Employer. Job Description #ITALLBEGINSWITHTALENT Would you like to join an innovative team creating technology to power groundbreaking insights in academic, clinical, pharma and biotech research? Our life science analytical and preparatory systems in mass cytometry and genomics can be found in leading academic institutions, clinical research laboratories, and pharmaceutical, biotech and ag-bio companies worldwide. Our mission is bold and ambitious, powering advancements in human health research that can change lives. Fluidigm is looking for a Molecular Biology Intern. A principle mission of the molecular biology group is to develop genomics product applications that utilize Fluidigm's proprietary microfluidics technology platform. The intern will participate in experimental planning, standard laboratory procedures, results analysis and reporting that supports the group's mission. Description: Participate in the planning and design of experimentsAdhere to all safety procedures and laboratoryUtilize good documentation practicesPerform laboratory activities that include but may not be limited to:nucleic acid extraction from formal-fixed, paraffin-embedded tissue sectionsspectrophotometric and fluorescent assayscapillary electrophoresis assayspolymerase chain reaction (PCR) amplification using Fluidigm's proprietary microfluidics technologynext generation DNA sequencing library preparation using Fluidigm's proprietary microfluidics technologyPerform results analysisPrepare report summaries Qualifications: Current good academic standing in an accredited college or universityBasic understanding of chemistry and biologyGood communication and organization skillsFamiliarity with the Microsoft Office suite of programsLaboratory experience very helpful Sounds good? Apply online with your resume! Fluidigm is an equal opportunity/affirmative action employer. We will consider all qualified applicants for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.PI107729856
Feb 14, 2019
FluidigmR&D Molecular Biology InternReq No.: 2019-2884Job Location: US-CA-South San FranciscoCategory: Research & DevelopmentType: InternWe are an AA/EEO/Veterans/Disabled Employer. Job Description #ITALLBEGINSWITHTALENT Would you like to join an innovative team creating technology to power groundbreaking insights in academic, clinical, pharma and biotech research? Our life science analytical and preparatory systems in mass cytometry and genomics can be found in leading academic institutions, clinical research laboratories, and pharmaceutical, biotech and ag-bio companies worldwide. Our mission is bold and ambitious, powering advancements in human health research that can change lives. Fluidigm is looking for a Molecular Biology Intern. A principle mission of the molecular biology group is to develop genomics product applications that utilize Fluidigm's proprietary microfluidics technology platform. The intern will participate in experimental planning, standard laboratory procedures, results analysis and reporting that supports the group's mission. Description: Participate in the planning and design of experimentsAdhere to all safety procedures and laboratoryUtilize good documentation practicesPerform laboratory activities that include but may not be limited to:nucleic acid extraction from formal-fixed, paraffin-embedded tissue sectionsspectrophotometric and fluorescent assayscapillary electrophoresis assayspolymerase chain reaction (PCR) amplification using Fluidigm's proprietary microfluidics technologynext generation DNA sequencing library preparation using Fluidigm's proprietary microfluidics technologyPerform results analysisPrepare report summaries Qualifications: Current good academic standing in an accredited college or universityBasic understanding of chemistry and biologyGood communication and organization skillsFamiliarity with the Microsoft Office suite of programsLaboratory experience very helpful Sounds good? Apply online with your resume! Fluidigm is an equal opportunity/affirmative action employer. We will consider all qualified applicants for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.PI107729856
Princeton UniversityDr. Mona Singh's laboratory within the Lewis-Sigler Institute for Integrative Genomics is seeking to hire a scientist in the area of computational biology at the rank of Associate Professional Specialist at Princeton University. The Computational Biologist will develop computational methods for predicting protein interactions. Candidates should have extensive experience with algorithmic computational biology and structural bioinformatics. In addition, they should have experience with creating robust software code. Essential Qualifications: - A PhD in a relevant discipline or related field.- Applicants must demonstrate an ability to carry out independent research.Preferred Qualifications: - Three years prior research experience in bioinformatics/computational biology.How to Apply:Applications must be submitted online, at the following URL: https://www.princeton.edu/acad-positions/position/10601Applications must include a curriculum vitae and contact information for three references. These positions are subject to the University's background check policy.PI107726108
Feb 14, 2019
Princeton UniversityDr. Mona Singh's laboratory within the Lewis-Sigler Institute for Integrative Genomics is seeking to hire a scientist in the area of computational biology at the rank of Associate Professional Specialist at Princeton University. The Computational Biologist will develop computational methods for predicting protein interactions. Candidates should have extensive experience with algorithmic computational biology and structural bioinformatics. In addition, they should have experience with creating robust software code. Essential Qualifications: - A PhD in a relevant discipline or related field.- Applicants must demonstrate an ability to carry out independent research.Preferred Qualifications: - Three years prior research experience in bioinformatics/computational biology.How to Apply:Applications must be submitted online, at the following URL: https://www.princeton.edu/acad-positions/position/10601Applications must include a curriculum vitae and contact information for three references. These positions are subject to the University's background check policy.PI107726108
Amyris, Inc.Location: Emeryville, CATeam: Manufacturing and Operations - Process Development & EngineeringWork Type: Full-TimeAmyris, a leader in industrial synthetic biology, uses its innovative bioscience solutions to achieve renewable products by converting plant sugars into hydrocarbon molecules. Amyris’ molecules are used in wide range of specialty & performance chemicals, flavors & fragrances and in applications ranging from cosmetics to biofuels. Learn more at www.amyris.com.As a VEVRAA Federal Contractor, Amyris is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Amyris complies with applicable state and local laws governing nondiscrimination in employment.For a full list of our current openings, please visit our website www.amyris.com.The Process Development team is seeking an Associate Scientist 3 with experience designing and analyzing early-stage microbial fermentations for the production of small molecules. This individual should be well-versed in fermentation science and also microbial physiology, secondary metabolism and biosynthetic pathways. We are specifically seeking an energetic, creative, and highly self-motivated individual that enjoys challenges in fermentation development. The successful candidate will interact closely with other fermentation scientists and engineers, downstream chemists and engineers, and upstream molecular biologists. ResponsibilitiesDesign and analyze fermentation experiments to maximize understanding and performance of strains and meet project goals for yield, productivity, purity specifications, and other process parameters.Optimize fermentation processes to maximize performance at the manufacturing scaleSupport technology transfer of fermentation processes to the pilot plant and manufacturing sites around the globeCommunicate with internal and external stakeholders through meetings and clearly written emails, reports and presentationsCollaborate with:Molecular biologists to understand the impact of genetic changes on strain performance Responsible for individual and co-worker safety and maintain safety as the highest priority by supporting and reinforcing procedures and policiesQualificationsRequires a BS in Chemical or Bio-Chemical Engineering/Microbiology/Biology/Food Science with at least 6 years of relevant experience or an MS with at least 4 years of experience. Experience designing and analyzing microbial fermentation experiments is required. Excellent interpersonal and communications skills are an essential characteristic of a successful candidate due to the highly collaborative nature of the positionAbility to work well in a fast-paced environment and balance multiple projectsStrong organization, problem solving, and quantitative analysis skills are criticalAbility to deliver clear, compelling and effective technical presentations to colleagues and managers PI107724464
Feb 14, 2019
Amyris, Inc.Location: Emeryville, CATeam: Manufacturing and Operations - Process Development & EngineeringWork Type: Full-TimeAmyris, a leader in industrial synthetic biology, uses its innovative bioscience solutions to achieve renewable products by converting plant sugars into hydrocarbon molecules. Amyris’ molecules are used in wide range of specialty & performance chemicals, flavors & fragrances and in applications ranging from cosmetics to biofuels. Learn more at www.amyris.com.As a VEVRAA Federal Contractor, Amyris is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Amyris complies with applicable state and local laws governing nondiscrimination in employment.For a full list of our current openings, please visit our website www.amyris.com.The Process Development team is seeking an Associate Scientist 3 with experience designing and analyzing early-stage microbial fermentations for the production of small molecules. This individual should be well-versed in fermentation science and also microbial physiology, secondary metabolism and biosynthetic pathways. We are specifically seeking an energetic, creative, and highly self-motivated individual that enjoys challenges in fermentation development. The successful candidate will interact closely with other fermentation scientists and engineers, downstream chemists and engineers, and upstream molecular biologists. ResponsibilitiesDesign and analyze fermentation experiments to maximize understanding and performance of strains and meet project goals for yield, productivity, purity specifications, and other process parameters.Optimize fermentation processes to maximize performance at the manufacturing scaleSupport technology transfer of fermentation processes to the pilot plant and manufacturing sites around the globeCommunicate with internal and external stakeholders through meetings and clearly written emails, reports and presentationsCollaborate with:Molecular biologists to understand the impact of genetic changes on strain performance Responsible for individual and co-worker safety and maintain safety as the highest priority by supporting and reinforcing procedures and policiesQualificationsRequires a BS in Chemical or Bio-Chemical Engineering/Microbiology/Biology/Food Science with at least 6 years of relevant experience or an MS with at least 4 years of experience. Experience designing and analyzing microbial fermentation experiments is required. Excellent interpersonal and communications skills are an essential characteristic of a successful candidate due to the highly collaborative nature of the positionAbility to work well in a fast-paced environment and balance multiple projectsStrong organization, problem solving, and quantitative analysis skills are criticalAbility to deliver clear, compelling and effective technical presentations to colleagues and managers PI107724464
SCS Engineers is an employee-owned environmental consulting and contracting firm that designs and implements sustainable environmental solutions. Our core capabilities are: solid and hazardous waste management, landfill gas, environmental due-diligence and assessment, brownfields redevelopment , site remediation, renewable energy, and regulatory compliance for businesses and municipalities responsible for protecting our air, water, and soil. Our employees take pride in their work, and together, we have the singular vision to be the environmental firm of choice for clients and our employee owners. If you thrive in a friendly, collaborative company and desire dynamic and challenging work among a team of innovative individuals, then SCS is the place for you. Do you have the innovative spirit we are looking for?Job Summary SCS Engineers is seeking a mid-level engineer, geologist or environmental professional in our Boca Raton, FL office to perform various activities related to environmental consulting. The ideal candidate will be a quick learner and self-motivated, is eager to learn, embraces teamwork, and has the desire to grow and develop professionally.Essential Duties and Responsibilities A mixture of office and filed work expected, with an emphasis on office work Phase I and II Environmental Site Assessments Multi-media sampling (soil, groundwater, surface water, sediment, air) and reporting Compliance monitoring, permitting, document preparation, and proposals Project Management of small to mid-scale projects Independently prepare environmental assessment reports Long field days and work at job sites throughout the southern FL area can be expected with this positionQualifications Bachelor's Degree in Environmental or Civil Engineering, Geology, Environmental Science or related field required Professional registration preferred (E.I.T./G.I.T.,P.E./P.G) 4-8 years of related environmental experience required Microsoft Office and computer programs (AutoCAD, Surfer, and/or ArcGIS preferred), field equipment experience preferred HAZWOPER training completed and up to date preferred Valid driver's license with driving record in good standing requiredAt SCS, you will have an opportunity to contribute to our strategic direction, help us continue to grow, and provide our clients with responsive, innovative, high quality client service. We offer excellent opportunities for career advancement and a competitive compensation package, including: medical, dental, vision, 401K, ESOP, paid holidays and PTO. SCS Engineers is an Equal Opportunity Employer (EOE). SCS provides equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disabled status.If you have questions, difficulty using our online system and/or you need an accommodation due to a disability then please contact us about your interest in employment at recruiting@scsengineers.com.PI107702164
Feb 13, 2019
SCS Engineers is an employee-owned environmental consulting and contracting firm that designs and implements sustainable environmental solutions. Our core capabilities are: solid and hazardous waste management, landfill gas, environmental due-diligence and assessment, brownfields redevelopment , site remediation, renewable energy, and regulatory compliance for businesses and municipalities responsible for protecting our air, water, and soil. Our employees take pride in their work, and together, we have the singular vision to be the environmental firm of choice for clients and our employee owners. If you thrive in a friendly, collaborative company and desire dynamic and challenging work among a team of innovative individuals, then SCS is the place for you. Do you have the innovative spirit we are looking for?Job Summary SCS Engineers is seeking a mid-level engineer, geologist or environmental professional in our Boca Raton, FL office to perform various activities related to environmental consulting. The ideal candidate will be a quick learner and self-motivated, is eager to learn, embraces teamwork, and has the desire to grow and develop professionally.Essential Duties and Responsibilities A mixture of office and filed work expected, with an emphasis on office work Phase I and II Environmental Site Assessments Multi-media sampling (soil, groundwater, surface water, sediment, air) and reporting Compliance monitoring, permitting, document preparation, and proposals Project Management of small to mid-scale projects Independently prepare environmental assessment reports Long field days and work at job sites throughout the southern FL area can be expected with this positionQualifications Bachelor's Degree in Environmental or Civil Engineering, Geology, Environmental Science or related field required Professional registration preferred (E.I.T./G.I.T.,P.E./P.G) 4-8 years of related environmental experience required Microsoft Office and computer programs (AutoCAD, Surfer, and/or ArcGIS preferred), field equipment experience preferred HAZWOPER training completed and up to date preferred Valid driver's license with driving record in good standing requiredAt SCS, you will have an opportunity to contribute to our strategic direction, help us continue to grow, and provide our clients with responsive, innovative, high quality client service. We offer excellent opportunities for career advancement and a competitive compensation package, including: medical, dental, vision, 401K, ESOP, paid holidays and PTO. SCS Engineers is an Equal Opportunity Employer (EOE). SCS provides equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disabled status.If you have questions, difficulty using our online system and/or you need an accommodation due to a disability then please contact us about your interest in employment at recruiting@scsengineers.com.PI107702164
SCS Engineers is an employee-owned environmental consulting and contracting firm that designs and implements sustainable environmental solutions. Our core capabilities are: solid and hazardous waste management, landfill gas, environmental due-diligence and assessment, brownfields redevelopment , site remediation, renewable energy, and regulatory compliance for businesses and municipalities responsible for protecting our air, water, and soil. Our employees take pride in their work, and together, we have the singular vision to be the environmental firm of choice for clients and our employee owners. If you thrive in a friendly, collaborative company and desire dynamic and challenging work among a team of innovative individuals, then SCS is the place for you. Do you have the innovative spirit we are looking for?Job Summary SCS Engineers is seeking an entry-level or staff level geologist or environmental professional in our Boca Raton, FL office to perform various activities related to environmental consulting. The ideal candidate will be a quick learner and self-motivated, is eager to learn, and has the desire to grow and develop professionally.Essential Duties and Responsibilities Approximately 50/50 field and office work expected Phase I and II Environmental Site Assessments Multi-media sampling (soil, groundwater, surface water, sediment, air) Compliance monitoring, permitting, document preparation, and participation in proposals Long field days and work at job sites throughout Southern FL can be expected at times with this positionQualifications Bachelor's Degree in Environmental or Civil Engineering, Geology, Environmental Science or related field required Training/certifications preferred (GIT or EIT) 0 to 4 years of environmental experience required Microsoft Office and computer programs (AutoCAD, Surfer, and/or ArcGIS preferred), field equipment experience preferred HAZWOPER training completed preferred Valid driver's license with driving record in good standing required Strong written and verbal communication, organizational and interpersonal skills; and the ability to work independently and with others; along with the ability to work on multiple simultaneous projects with successful time management is desireAt SCS, you will have an opportunity to contribute to our strategic direction, help us continue to grow, and provide our clients with responsive, innovative, high quality client service. We offer excellent opportunities for career advancement and a competitive compensation package, including: medical, dental, vision, 401K, ESOP, paid holidays and PTO. SCS Engineers is an Equal Opportunity Employer (EOE). SCS provides equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disabled status.If you have questions, difficulty using our online system and/or you need an accommodation due to a disability then please contact us about your interest in employment at recruiting@scsengineers.com.PI107701316
Feb 13, 2019
SCS Engineers is an employee-owned environmental consulting and contracting firm that designs and implements sustainable environmental solutions. Our core capabilities are: solid and hazardous waste management, landfill gas, environmental due-diligence and assessment, brownfields redevelopment , site remediation, renewable energy, and regulatory compliance for businesses and municipalities responsible for protecting our air, water, and soil. Our employees take pride in their work, and together, we have the singular vision to be the environmental firm of choice for clients and our employee owners. If you thrive in a friendly, collaborative company and desire dynamic and challenging work among a team of innovative individuals, then SCS is the place for you. Do you have the innovative spirit we are looking for?Job Summary SCS Engineers is seeking an entry-level or staff level geologist or environmental professional in our Boca Raton, FL office to perform various activities related to environmental consulting. The ideal candidate will be a quick learner and self-motivated, is eager to learn, and has the desire to grow and develop professionally.Essential Duties and Responsibilities Approximately 50/50 field and office work expected Phase I and II Environmental Site Assessments Multi-media sampling (soil, groundwater, surface water, sediment, air) Compliance monitoring, permitting, document preparation, and participation in proposals Long field days and work at job sites throughout Southern FL can be expected at times with this positionQualifications Bachelor's Degree in Environmental or Civil Engineering, Geology, Environmental Science or related field required Training/certifications preferred (GIT or EIT) 0 to 4 years of environmental experience required Microsoft Office and computer programs (AutoCAD, Surfer, and/or ArcGIS preferred), field equipment experience preferred HAZWOPER training completed preferred Valid driver's license with driving record in good standing required Strong written and verbal communication, organizational and interpersonal skills; and the ability to work independently and with others; along with the ability to work on multiple simultaneous projects with successful time management is desireAt SCS, you will have an opportunity to contribute to our strategic direction, help us continue to grow, and provide our clients with responsive, innovative, high quality client service. We offer excellent opportunities for career advancement and a competitive compensation package, including: medical, dental, vision, 401K, ESOP, paid holidays and PTO. SCS Engineers is an Equal Opportunity Employer (EOE). SCS provides equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disabled status.If you have questions, difficulty using our online system and/or you need an accommodation due to a disability then please contact us about your interest in employment at recruiting@scsengineers.com.PI107701316
Clemson UniversityLocation FMOFull/Part Time Full-TimeRegular/Temporary RegularJOB SUMMARY: Performs various arboricultural duties including, technical strategies of tree maintenance, disease treatment and disease prevention. Assists with maintaining and the inventory of trees within each designated zone. Performs other duties as assigned.JOB DUTIES: 50% - Essential - Ground Duties:Performs ground pruning using pole saws, battery and gas powered saws. Removes tree, stumps, fallen limbs and related debris. Plants trees. Sprays, stakes and maintains trees.30% - Essential - Aerial Duties:Uses aerial lift and approved techniques to remove and prune trees in order to provide clearance of streets, sidewalks and signs. Ensures the continued health of trees to reduce the risk of tree failure.15% - Essential - Equipment Operation and Maintenance:Operates and maintains all arboricultural equipment such as boom trucks, lifts, chippers, stump grinders, dump trucks, power tool and any arboricultural related equipment.5% - Essential - Weather Related Cleanup and Clearing:Operate equipment that is needed to clean up and clear roadways and sidewalks during weather events.MINIMUM REQUIREMENTS: A high school diploma and trade experience that is directly related to the area of employment.RESPONSIBILITIES: JOB KNOWLEDGEFirm Job Knowledge - Firm working knowledge of concepts, practices and procedures and ability to use in varied situationsSUPERVISORY RESPONSIBILITIESNo Supervisory Duties - Not responsible for supervising employees.BUDGETARY RESPONSIBILITIESNo Budget Responsibilities - No fiscal responsibility for the department's budget.PHYSICAL REQUIREMENTS: 75% - Communicate, converse, give direction, express oneself 75% - Recognize or inspect visually75% - Perceive, observe, clarity of vision70% - Stand for prolonged period 70% - Walk or move about 70% - Use hands or feet to operate or handle machinery, equipment, etc 70% - Extends hands or arms in any direction 50% - Move, transport, raise or lower 25% - Position self to accomplish task (i.e. stoop, kneel, crawl) 25% - Sit (stationary position) for prolonged period 10% - Ascend or descend (i.e. stairs, ladder)WORKING CONDITIONS: 60% - Mechanical Hazards 50% - Exposure to heat or cold 50% - Exposure to dust/fumes 50% - Noise 40% - Vibration 40% - Burn hazards20% - Wet or humid20% - Chemical hazardsPREFERRED REQUIREMENTS: Licenses - Commercial Driver's License Class A or BLicenses - Drivers License Class D normal Work Exp 1+ yearsWORK SCHEDULE: Standard Hrs: 40; Band: 04 ($ 28,600.00 - $ 36,700.00)APPLICATION DEADLINE: February 25, 2019JOB LOCATION: Clemson, SCCLOSING STATEMENT: Clemson University is an AA/EEO employer and does not discriminate against any person or group on the basis of age, color, disability, gender, pregnancy, national origin, race, religion, sexual orientation, veteran status or genetic information. Clemson University is building a culturally diverse faculty and staff committed to working in a multicultural environment and encourages applications from minorities and women.PI107700920
Feb 13, 2019
Clemson UniversityLocation FMOFull/Part Time Full-TimeRegular/Temporary RegularJOB SUMMARY: Performs various arboricultural duties including, technical strategies of tree maintenance, disease treatment and disease prevention. Assists with maintaining and the inventory of trees within each designated zone. Performs other duties as assigned.JOB DUTIES: 50% - Essential - Ground Duties:Performs ground pruning using pole saws, battery and gas powered saws. Removes tree, stumps, fallen limbs and related debris. Plants trees. Sprays, stakes and maintains trees.30% - Essential - Aerial Duties:Uses aerial lift and approved techniques to remove and prune trees in order to provide clearance of streets, sidewalks and signs. Ensures the continued health of trees to reduce the risk of tree failure.15% - Essential - Equipment Operation and Maintenance:Operates and maintains all arboricultural equipment such as boom trucks, lifts, chippers, stump grinders, dump trucks, power tool and any arboricultural related equipment.5% - Essential - Weather Related Cleanup and Clearing:Operate equipment that is needed to clean up and clear roadways and sidewalks during weather events.MINIMUM REQUIREMENTS: A high school diploma and trade experience that is directly related to the area of employment.RESPONSIBILITIES: JOB KNOWLEDGEFirm Job Knowledge - Firm working knowledge of concepts, practices and procedures and ability to use in varied situationsSUPERVISORY RESPONSIBILITIESNo Supervisory Duties - Not responsible for supervising employees.BUDGETARY RESPONSIBILITIESNo Budget Responsibilities - No fiscal responsibility for the department's budget.PHYSICAL REQUIREMENTS: 75% - Communicate, converse, give direction, express oneself 75% - Recognize or inspect visually75% - Perceive, observe, clarity of vision70% - Stand for prolonged period 70% - Walk or move about 70% - Use hands or feet to operate or handle machinery, equipment, etc 70% - Extends hands or arms in any direction 50% - Move, transport, raise or lower 25% - Position self to accomplish task (i.e. stoop, kneel, crawl) 25% - Sit (stationary position) for prolonged period 10% - Ascend or descend (i.e. stairs, ladder)WORKING CONDITIONS: 60% - Mechanical Hazards 50% - Exposure to heat or cold 50% - Exposure to dust/fumes 50% - Noise 40% - Vibration 40% - Burn hazards20% - Wet or humid20% - Chemical hazardsPREFERRED REQUIREMENTS: Licenses - Commercial Driver's License Class A or BLicenses - Drivers License Class D normal Work Exp 1+ yearsWORK SCHEDULE: Standard Hrs: 40; Band: 04 ($ 28,600.00 - $ 36,700.00)APPLICATION DEADLINE: February 25, 2019JOB LOCATION: Clemson, SCCLOSING STATEMENT: Clemson University is an AA/EEO employer and does not discriminate against any person or group on the basis of age, color, disability, gender, pregnancy, national origin, race, religion, sexual orientation, veteran status or genetic information. Clemson University is building a culturally diverse faculty and staff committed to working in a multicultural environment and encourages applications from minorities and women.PI107700920
Amyris, Inc.Location: Leland, NCTeam: Manufacturing and Operations - North Carolina PlantWork Type: Full-TimeAmyris, a leader in industrial synthetic biology, uses its innovative bioscience solutions to achieve renewable products by converting plant sugars into hydrocarbon molecules. Amyris’ molecules are used in wide range of specialty & performance chemicals, flavors & fragrances and in applications ranging from cosmetics to biofuels. Learn more at www.amyris.com.As a VEVRAA Federal Contractor, Amyris is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Amyris complies with applicable state and local laws governing nondiscrimination in employment.For a full list of our current openings, please visit our website www.amyris.com.Conduct chemical and physical laboratory tests to assist in making qualitative and quantitative analysis of solid and liquid products. This is a Quality Control/Quality Assurance position in which the Chemist will perform in-process and final product testing as well as the drafting of quality related SOPs. The Chemist must be willing to work some overtime, including weekends and holidays.ResponsibilitiesProvide and maintain a safe work environment by participating in safety programs, committees, or teams, and by conducting safety audits. Follow all company policies and procedures pertaining to ISO 22716-Good Manufacturing Procedures (GMPs) guidelines for cosmetics.Maintain clean instruments and equipment. Compile and interpret results of tests and analyses. Maintain an inventory of materials to maintain supplies. Prepare chemical solutions for products and processes following standardized formulas. Monitor product quality to ensure compliance to standards and specifications. Set up and conduct chemical and physical tests and analyses using techniques and instruments such as gas chromatography, auto titrators, KF titrators, tintometer, refractometer, viscometer, and others.Provide technical support and assistance to other chemists, mangers and engineers. Conduct sampling and analysis to maintain quality standards of raw materials, chemical intermediates, and products.Perform validation of analytical testing methods.Troubleshoot analytical instrumentation.Perform weigh outs of Raw Materials.Assist in the technical transfer of analytical methods Supervise and train QC technicians as needed. Perform inspections on empty and filled containers.Perform Release Testing on Finished Products.Assist in performing and analyzing process development experiments-which involves the safe use of standard laboratory glassware, equipment and autoclaves commonly used for organic, organometallic and inorganic synthesis. Second Shift position - (4pm - 12:am) QualificationsQualifications include a minimum of a BS in chemistry or related field. A concentration in analytical chemistry is desired, but not required. Experience in method validation and development is desired as well as troubleshooting of analytical instrumentation and software. Embrace Amyris Core ValuesAdherence to Amyris Safety Policies and ProceduresPhysical requirementsMust be available for flexible schedule including working days/nights and overtime on weekends. While performing the duties of this job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel. Specific vision abilities required by this job include close vision, color vision, depth perception, and ability to adjust focus. Must also be able to safely lift 25-30 pounds and work both indoors and outdoors in intense weather conditions. Must possess the ability to wear a respirator. PI107683487
Feb 13, 2019
Amyris, Inc.Location: Leland, NCTeam: Manufacturing and Operations - North Carolina PlantWork Type: Full-TimeAmyris, a leader in industrial synthetic biology, uses its innovative bioscience solutions to achieve renewable products by converting plant sugars into hydrocarbon molecules. Amyris’ molecules are used in wide range of specialty & performance chemicals, flavors & fragrances and in applications ranging from cosmetics to biofuels. Learn more at www.amyris.com.As a VEVRAA Federal Contractor, Amyris is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Amyris complies with applicable state and local laws governing nondiscrimination in employment.For a full list of our current openings, please visit our website www.amyris.com.Conduct chemical and physical laboratory tests to assist in making qualitative and quantitative analysis of solid and liquid products. This is a Quality Control/Quality Assurance position in which the Chemist will perform in-process and final product testing as well as the drafting of quality related SOPs. The Chemist must be willing to work some overtime, including weekends and holidays.ResponsibilitiesProvide and maintain a safe work environment by participating in safety programs, committees, or teams, and by conducting safety audits. Follow all company policies and procedures pertaining to ISO 22716-Good Manufacturing Procedures (GMPs) guidelines for cosmetics.Maintain clean instruments and equipment. Compile and interpret results of tests and analyses. Maintain an inventory of materials to maintain supplies. Prepare chemical solutions for products and processes following standardized formulas. Monitor product quality to ensure compliance to standards and specifications. Set up and conduct chemical and physical tests and analyses using techniques and instruments such as gas chromatography, auto titrators, KF titrators, tintometer, refractometer, viscometer, and others.Provide technical support and assistance to other chemists, mangers and engineers. Conduct sampling and analysis to maintain quality standards of raw materials, chemical intermediates, and products.Perform validation of analytical testing methods.Troubleshoot analytical instrumentation.Perform weigh outs of Raw Materials.Assist in the technical transfer of analytical methods Supervise and train QC technicians as needed. Perform inspections on empty and filled containers.Perform Release Testing on Finished Products.Assist in performing and analyzing process development experiments-which involves the safe use of standard laboratory glassware, equipment and autoclaves commonly used for organic, organometallic and inorganic synthesis. Second Shift position - (4pm - 12:am) QualificationsQualifications include a minimum of a BS in chemistry or related field. A concentration in analytical chemistry is desired, but not required. Experience in method validation and development is desired as well as troubleshooting of analytical instrumentation and software. Embrace Amyris Core ValuesAdherence to Amyris Safety Policies and ProceduresPhysical requirementsMust be available for flexible schedule including working days/nights and overtime on weekends. While performing the duties of this job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel. Specific vision abilities required by this job include close vision, color vision, depth perception, and ability to adjust focus. Must also be able to safely lift 25-30 pounds and work both indoors and outdoors in intense weather conditions. Must possess the ability to wear a respirator. PI107683487
University of DelawareJob Title Associate ScientistJob ID 106156Location Newark, DEUnder limited direction, the Associate Scientist will lead and manage a newly formed Flow Cytometry lab that is embedded in a satellite site of the Bio-Imaging Center. In this role, the Associate Scientist will independently manage and lead all of the flow cytometry and fluorescence activated cell sorting (FACS) day-to-day operation, research project consultation, and training of users. The Associate Scientist will be able to determine how flow cytometry or FACS advances a research project and will provide high-level intellectual contributions in experimental design and analysis of multi-color labeling protocols. MAJOR RESPONSIBILITIES: Oversee the daily operations of flow cytometry and FACS to provide high quality fee-for-service access. Operate and maintain analysis/sorting instrumentation, ancillary equipment, and data analysis workstations. Maintain knowledge of current technological developments and trends in the area of flow cytometry and FACS. Evaluate and recommend new technologies. Develop, adapt, or adopt new protocols, specialized methods, multicolor panels, and assay formats. Perform Flow and FACS procedures for investigators as needed. Train new users on flow cytometry and develop a training regime consisting of hands-on training, a user manual, and workshops. Conduct scientific outreach to build and maintain a vibrant, broad user-base. Direct projects or manage specialized segments of highly technical or complex studies. Collaborate with principal investigators and users on design, analysis, application and reporting of research projects. Assist with other instrumentation and services within the Bio-Imaging Center as needed. QUALIFICATIONS: Master's degree in related discipline and five years of experience in Biology/Chemistry/Biophysics or related field, or an equivalent combination of education and experience. Ph.D. preferred. In-depth and up to-date knowledge of flow cytometry and FACS. Proficiency with BD analyzers and FACS/Diva data analysis. Ability to adhere to and enforce safety procedures. Ability to follow and/or optimize research methodologies and protocols. Effective leadership, communication and organizational skills. Strong interpersonal skills with a service-oriented approach to assisting users in a core facility. Ability to work independently as well as a member of a team. Ability to train and instruct others, and interact effectively well with people of all ages and diverse backgrounds. Motivation to learn new techniques, flexibility, and ability to interact with a diverse group of research personnel. Experience with imaging technologies, including but not limited to whole animal imaging, intravital microscopy, microCT, or ultrasound imaging is desirable. PI107689128
Feb 13, 2019
University of DelawareJob Title Associate ScientistJob ID 106156Location Newark, DEUnder limited direction, the Associate Scientist will lead and manage a newly formed Flow Cytometry lab that is embedded in a satellite site of the Bio-Imaging Center. In this role, the Associate Scientist will independently manage and lead all of the flow cytometry and fluorescence activated cell sorting (FACS) day-to-day operation, research project consultation, and training of users. The Associate Scientist will be able to determine how flow cytometry or FACS advances a research project and will provide high-level intellectual contributions in experimental design and analysis of multi-color labeling protocols. MAJOR RESPONSIBILITIES: Oversee the daily operations of flow cytometry and FACS to provide high quality fee-for-service access. Operate and maintain analysis/sorting instrumentation, ancillary equipment, and data analysis workstations. Maintain knowledge of current technological developments and trends in the area of flow cytometry and FACS. Evaluate and recommend new technologies. Develop, adapt, or adopt new protocols, specialized methods, multicolor panels, and assay formats. Perform Flow and FACS procedures for investigators as needed. Train new users on flow cytometry and develop a training regime consisting of hands-on training, a user manual, and workshops. Conduct scientific outreach to build and maintain a vibrant, broad user-base. Direct projects or manage specialized segments of highly technical or complex studies. Collaborate with principal investigators and users on design, analysis, application and reporting of research projects. Assist with other instrumentation and services within the Bio-Imaging Center as needed. QUALIFICATIONS: Master's degree in related discipline and five years of experience in Biology/Chemistry/Biophysics or related field, or an equivalent combination of education and experience. Ph.D. preferred. In-depth and up to-date knowledge of flow cytometry and FACS. Proficiency with BD analyzers and FACS/Diva data analysis. Ability to adhere to and enforce safety procedures. Ability to follow and/or optimize research methodologies and protocols. Effective leadership, communication and organizational skills. Strong interpersonal skills with a service-oriented approach to assisting users in a core facility. Ability to work independently as well as a member of a team. Ability to train and instruct others, and interact effectively well with people of all ages and diverse backgrounds. Motivation to learn new techniques, flexibility, and ability to interact with a diverse group of research personnel. Experience with imaging technologies, including but not limited to whole animal imaging, intravital microscopy, microCT, or ultrasound imaging is desirable. PI107689128
Description:Job Summary: To deputize for the QA/RA Director(s) in their absence. To act as a responsible Person as required by regulation. To have direct responsibility for technical files (STED), international registration and to keep the company abreast of new regulations that are applicable. To assist with 510(k) and clinical trials.Quality Assurance responsibilities are risk management, auditing and new product development design control although other duties may be assigned as required.Responsibilities: Sole: Construct and maintain Standard Technical files as evidence of compliance to European and US regulations and other authorities as required.Sole: To produce reports and training literature on new regulations.Sole: To oversee the RoHS technical file construction and to verify their compliance.Sole: To produce post market surveillance reports and trending.Joint: To ensure risk management files are compliant to ISO14971 and are current.Joint: To give strategic direction for 510(k) and clinical trials.joint: As required, to be a contact person for European authorities and FDA.Joint: To take on and manage discrete quality or regulatory projects.Joint: To be involved in and to manage planned site inspections and Audits.Joint: To be the Regulatory subject matter expert for design control projects.Joint: To conduct secondary and third party audits.Joint: To act as one of company's Qualified Person (responsibilities are defined by regulation).Joint: to be a Subject Matter Expert for vigilance and reportable events.Joint: To write procedures in support of Quality, Regulatory and Clinical processes.Joint: To train Dynex personnel on quality and regulatory topics.Sole: to act as the Quality Representative for all Dynex European sites.Joint: to assist with shipping compliance issues.Supervisory Responsibilities: Direct report of Regulatory Associate(s). Responsible for project managing discrete projects.Success Factors: To be able to work independently and to manage project teams. To stay up to date with the current regulatory changes. To be able to communicate effectively through both written media and verbally. Strong mediation and negotiation skills. It would be beneficial to have formal qualification in auditing and project management..Requirements:Minimum Qualifications/Education: Specific knowledge of International standards and regulations inclusive of ISO, FDA, and EC/98/79 IVDD. A minimum of 5 years working with IVD devices with a scientific or engineering degree.Computer Skills: Computer literacy in Windows, Word, Excel, Power point and Vision.Work Environment: Office.Physical Requirements: Must be able to meet National Institute for Occupational Safety & Health (NIOSH) Standards.PI107634619
Feb 10, 2019
Description:Job Summary: To deputize for the QA/RA Director(s) in their absence. To act as a responsible Person as required by regulation. To have direct responsibility for technical files (STED), international registration and to keep the company abreast of new regulations that are applicable. To assist with 510(k) and clinical trials.Quality Assurance responsibilities are risk management, auditing and new product development design control although other duties may be assigned as required.Responsibilities: Sole: Construct and maintain Standard Technical files as evidence of compliance to European and US regulations and other authorities as required.Sole: To produce reports and training literature on new regulations.Sole: To oversee the RoHS technical file construction and to verify their compliance.Sole: To produce post market surveillance reports and trending.Joint: To ensure risk management files are compliant to ISO14971 and are current.Joint: To give strategic direction for 510(k) and clinical trials.joint: As required, to be a contact person for European authorities and FDA.Joint: To take on and manage discrete quality or regulatory projects.Joint: To be involved in and to manage planned site inspections and Audits.Joint: To be the Regulatory subject matter expert for design control projects.Joint: To conduct secondary and third party audits.Joint: To act as one of company's Qualified Person (responsibilities are defined by regulation).Joint: to be a Subject Matter Expert for vigilance and reportable events.Joint: To write procedures in support of Quality, Regulatory and Clinical processes.Joint: To train Dynex personnel on quality and regulatory topics.Sole: to act as the Quality Representative for all Dynex European sites.Joint: to assist with shipping compliance issues.Supervisory Responsibilities: Direct report of Regulatory Associate(s). Responsible for project managing discrete projects.Success Factors: To be able to work independently and to manage project teams. To stay up to date with the current regulatory changes. To be able to communicate effectively through both written media and verbally. Strong mediation and negotiation skills. It would be beneficial to have formal qualification in auditing and project management..Requirements:Minimum Qualifications/Education: Specific knowledge of International standards and regulations inclusive of ISO, FDA, and EC/98/79 IVDD. A minimum of 5 years working with IVD devices with a scientific or engineering degree.Computer Skills: Computer literacy in Windows, Word, Excel, Power point and Vision.Work Environment: Office.Physical Requirements: Must be able to meet National Institute for Occupational Safety & Health (NIOSH) Standards.PI107634619
Integrated DNA TechnologiesID 2019-4557Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 9 hours agoShift/Schedule M-F 12pm - 9pmOverview The Manufacturing Chemist efficiently produces high quality materials for use in IDT's production labs.ResponsibilitiesEssential Functions:Monitors inventory of the group effectively; utilizing the ERP system. Follows the current processes for manufacturing, storage and transportation methods.Adheres to current RCRA and hazardous material DOT regulations and follows hazardous material spill response protocols.Gathers, interprets and analyzes oligo data.Ensures materials are prepared in a timely fashion.Changes and dispenses materials for production, as necessary.Participates in customer and regulatory audits, as necessary.Maintains accurate and detailed product, process, instrument and training records.Adheres to all departmental protocols, rules, contamination controls, and safety procedures and understands the requirements of ISO 9001, ISO 13485 and ISO 14001.Demonstrates behavior consistent with the Integrated DNA Technologies Core Values. Performs other duties as assigned.Department/Group Specific Essential Functions:Utilizes a full face respirator, as required.
Feb 10, 2019
Integrated DNA TechnologiesID 2019-4557Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 9 hours agoShift/Schedule M-F 12pm - 9pmOverview The Manufacturing Chemist efficiently produces high quality materials for use in IDT's production labs.ResponsibilitiesEssential Functions:Monitors inventory of the group effectively; utilizing the ERP system. Follows the current processes for manufacturing, storage and transportation methods.Adheres to current RCRA and hazardous material DOT regulations and follows hazardous material spill response protocols.Gathers, interprets and analyzes oligo data.Ensures materials are prepared in a timely fashion.Changes and dispenses materials for production, as necessary.Participates in customer and regulatory audits, as necessary.Maintains accurate and detailed product, process, instrument and training records.Adheres to all departmental protocols, rules, contamination controls, and safety procedures and understands the requirements of ISO 9001, ISO 13485 and ISO 14001.Demonstrates behavior consistent with the Integrated DNA Technologies Core Values. Performs other duties as assigned.Department/Group Specific Essential Functions:Utilizes a full face respirator, as required.
Integrated DNA TechnologiesID 2019-4556Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 14 hours agoShift/Schedule MTWThF 7:00A-4:00P (United States of America)Overview The Custom Quality Control Analyst I ensures the quality of processes and products in support of all manufacturing areas within Integrated DNA Technologies. ResponsibilitiesDepartmental Specific Functions:Operates a variety of equipment related to qPCR and ddPCR; including sample handling equipment and other general laboratory equipment. Essential Functions:Analyzes data and information for quality, consistency, and accuracy.Handles sample and reagent preparations for required assays in a careful manner.Uses computers and a variety of custom software in a windows based environment to maintain accurate and detailed sample and instrument records.Demonstrates manual dexterity and technical proficiency with pipetting and sample handling.Communicates with all levels of peers and management to ensure detailed information transfer.Adheres to all departmental protocols, rules, contamination controls, and safety procedures.Understands and complies with the ISO 9001, ISO 14001 and ISO13485 requirements.Performs routine maintenance on equipment and participates in laboratory cleanliness and organization.Organizes and appropriately prioritizes workload to ensure efficiency in product manufacture.Executes multiple processes simultaneously (multi-tasks) to ensure efficiency in sample handling.Demonstrates behavior consistent with the Integrated DNA Technologies Core Values.Performs other duties as assigned.
Feb 10, 2019
Integrated DNA TechnologiesID 2019-4556Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 14 hours agoShift/Schedule MTWThF 7:00A-4:00P (United States of America)Overview The Custom Quality Control Analyst I ensures the quality of processes and products in support of all manufacturing areas within Integrated DNA Technologies. ResponsibilitiesDepartmental Specific Functions:Operates a variety of equipment related to qPCR and ddPCR; including sample handling equipment and other general laboratory equipment. Essential Functions:Analyzes data and information for quality, consistency, and accuracy.Handles sample and reagent preparations for required assays in a careful manner.Uses computers and a variety of custom software in a windows based environment to maintain accurate and detailed sample and instrument records.Demonstrates manual dexterity and technical proficiency with pipetting and sample handling.Communicates with all levels of peers and management to ensure detailed information transfer.Adheres to all departmental protocols, rules, contamination controls, and safety procedures.Understands and complies with the ISO 9001, ISO 14001 and ISO13485 requirements.Performs routine maintenance on equipment and participates in laboratory cleanliness and organization.Organizes and appropriately prioritizes workload to ensure efficiency in product manufacture.Executes multiple processes simultaneously (multi-tasks) to ensure efficiency in sample handling.Demonstrates behavior consistent with the Integrated DNA Technologies Core Values.Performs other duties as assigned.
National Audubon SocietyJob Locations US-MO-West AltonType Seasonal, Full-TimeJob Category Office/Support ServicesID 2019-3933City West AltonState/Province MOOverview Now in its second century, Audubon is dedicated to protecting birds and other wildlife and the habitat that supports them. Audubon’s mission is engaging people in bird conservation on a hemispheric scale through science, policy, education and on-the-ground conservation action. By mobilizing and aligning its network of Chapters, Centers, State and Important Bird Area programs in the four major migratory flyways in the Americas, the organization will bring the full power of Audubon to bear on protecting common and threatened bird species and the critical habitat they need to survive. And as part of BirdLife International, Audubon will join people in over 100 in-country organizations all working to protect a network of Important Bird Areas around the world, leveraging the impact of actions they take at a local level. What defines Audubon’s unique value is a powerful grassroots network of nearly 500 local chapters, 23 state offices, 41 Audubon Centers, Important Bird Area Programs in 50 states, and 700 staff across the country. Audubon is a federal contractor and an Equal Opportunity Employer (EOE).Position Summary The Audubon Center is seeking an Avian Territory Mapping Survey Technician to assist with avian monitoring (avian territory mapping surveys).Essential Functions • Monitor avian species presence in the field by both sight and sound • Data management and data entry tasks• Assist with facilitation of monitoring logisticsQualifications and Experience • Bachelor’s degree in Biology, Ecology, Conservation, Natural Sciences, or related field required• Experience with avian territory mapping techniques• Identification of Midwestern birds by sight and sound desired• Attention to detail and accuracy when gathering data • Strong organizational and communication skills• Ability to work independently and as part of a team• Ability to work early hours • Ability to work outdoors in varying climates and conditions (heat, biting insects, wet terrain) • Ability to work effectively with volunteers and/or interns to when performing point count surveys• Proficiency with Microsoft Office Suite• Must possess valid driver’s license• Experience with ArcGIS Collector desiredPI107612572
Feb 10, 2019
National Audubon SocietyJob Locations US-MO-West AltonType Seasonal, Full-TimeJob Category Office/Support ServicesID 2019-3933City West AltonState/Province MOOverview Now in its second century, Audubon is dedicated to protecting birds and other wildlife and the habitat that supports them. Audubon’s mission is engaging people in bird conservation on a hemispheric scale through science, policy, education and on-the-ground conservation action. By mobilizing and aligning its network of Chapters, Centers, State and Important Bird Area programs in the four major migratory flyways in the Americas, the organization will bring the full power of Audubon to bear on protecting common and threatened bird species and the critical habitat they need to survive. And as part of BirdLife International, Audubon will join people in over 100 in-country organizations all working to protect a network of Important Bird Areas around the world, leveraging the impact of actions they take at a local level. What defines Audubon’s unique value is a powerful grassroots network of nearly 500 local chapters, 23 state offices, 41 Audubon Centers, Important Bird Area Programs in 50 states, and 700 staff across the country. Audubon is a federal contractor and an Equal Opportunity Employer (EOE).Position Summary The Audubon Center is seeking an Avian Territory Mapping Survey Technician to assist with avian monitoring (avian territory mapping surveys).Essential Functions • Monitor avian species presence in the field by both sight and sound • Data management and data entry tasks• Assist with facilitation of monitoring logisticsQualifications and Experience • Bachelor’s degree in Biology, Ecology, Conservation, Natural Sciences, or related field required• Experience with avian territory mapping techniques• Identification of Midwestern birds by sight and sound desired• Attention to detail and accuracy when gathering data • Strong organizational and communication skills• Ability to work independently and as part of a team• Ability to work early hours • Ability to work outdoors in varying climates and conditions (heat, biting insects, wet terrain) • Ability to work effectively with volunteers and/or interns to when performing point count surveys• Proficiency with Microsoft Office Suite• Must possess valid driver’s license• Experience with ArcGIS Collector desiredPI107612572