29 jobs found

Environmental Analyst (Monitoring)Staten Island, New York The Interstate Environmental Commission is seeking an Environmental Analyst to serve as project manager for IEC’s Western Long Island Sound Study Monitoring Program. The incumbent will coordinate monitoring surveys, supervise field monitoring, assist with laboratory analyses, prepare and distribute data summaries and reports, as well as support IEC’s other programs related to ambient water quality monitoring and citizen science. To apply, send a cover letter, resume, a list of references, and a short writing sample to jobs@iec-nynjct.org by September 25, 2018. Please reference position number 19-IEC-002 in the e-mail subject line.

Responsibilities:The Clinical Data Scientist at Otsuka will support a diverse array of initiatives including advanced computational modeling, clinical development (with particular focus on digital programs), and software development projects. Paramount to this role is the ability to support clinical programs with appropriate analytical strategies.Work closely with stakeholders interfacing with clinical and real-world data to identify, enhance, and support the quantitative and technological needs for all Otsuka projectsManaging software development projects at various levelsReviewing/planning clinical studies across multiple CNS programs, and conducting analyses related to time series modeling, supervised and unsupervised learning techniques, Bayesian methodologies, and othersProvide statistical and modeling support for planning and implementing clinical and real-world evidence studies/programs to meet the value/evidence needs of payers, health systems, clinicians, and patients.Provide solutions of clinical and economic utility by leveraging internal, external and real-world data sources.Guide evidence-based product development (digital/non-digital) by extracting therapeutic intelligence from such data sourcesTravel (up to 15-20%) Qualifications:Qualifications Required:A PhD in Pharmaceutical Science, Statistics, Engineering, Mathematics, or a related quantitative field with 0- 5 of years of post-graduate experienceKnowledge of existing and upcoming statistical methods (supervised and unsupervised) in pharmaceutical data analysisProficiency with programming in software such as Python, R, MATLAB, SAS, SQL etc.Knowledge of pharmaceutical modeling tools such as NONMEM, Monolix, Phoenix NMLE, etc.Knowledge of clinical development and clinical trial executionMust be agile to grow in new directions, acquire new skills, and work with a team of scientists and practitioners from different functional areas to solve problems and create solutions of clinical and economic utility.Must be able to bring insights to stakeholders with ability to extract therapeutic intelligence by leveraging internal, external, and real-world data sources.Excellent communication skillsPreferred:Knowledge of, and experience with, real world databasesKnowledge of current and emerging 'big data' technologiesOtsuka Pharmaceutical Company is a global healthcare company with the corporate philosophy: "Otsuka-people creating new products for better health worldwide." Otsuka researches, develops, manufactures and markets innovative products, with a focus on pharmaceutical products to meet unmet medical needs and nutraceutical products for the maintenance of everyday health.In pharmaceuticals, Otsuka is a leader in the challenging area of mental health and also has research programs on several under-addressed diseases including tuberculosis, a significant global public health issue. These commitments illustrate how Otsuka is a "big venture" company at heart, applying a youthful spirit of creativity in everything it does.Otsuka Pharmaceutical Company is a subsidiary of Otsuka Holdings Co., Ltd. headquartered in Tokyo, Japan. The Otsuka group of companies employed 45,000 people worldwide and had consolidated sales of approximately USD 11 billion ( 9.9 billion) in 2016. All Otsuka stories start by taking the road less travelled. Learn more about Otsuka Pharmaceutical Company on its global website at www.otsuka.co.jp/en. Learn more about Otsuka in the U.S. at www.otsuka-us.com.PI103943175

Integrated DNA TechnologiesID 2018-4001Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 12 hours agoShift/Schedule MTWThF 12:00P-9:00P (United States of America)Overview The Chemical Technician efficiently produces high quality reagents for use in IDT's production labs. ResponsibilitiesMonitors inventory of the Chemical Processing group effectively, utilizing the ERP system. Participates in customer and regulatory audits as necessary.Maintains accurate and detailed product, process, instrument and training records.Prepares materials according to documented procedures using standard lab equipmentAdheres to all departmental protocols, rules, contamination controls, and safety procedures and understands the requirements of ISO 9001, ISO 13485 and ISO 14001.Participates in the Hazardous Material Spill Response Team.Demonstrates and upholds behavior consistent with the Integrated DNA Technologies Core Values and delivers the Integrated DNA Technologies experience to customers and other business associates.Other duties as assigned.

Myriad Genetics, IncMyriad is an equal opportunity employer and as such, affirms in policy and practice to recruit, hire, train and promote, in all job classifications without regard to race, color, religion, gender, age, sexual orientation, gender identity, national origin, disability status or status as a protected veteran. Reasonable accommodation will be provided for qualified individuals with disabilities and disabled veterans in job application procedures. We believe that diversity lends a regional, national, and global advantage to the clients we serve. Our workforce consists of dynamic individuals, with a range of backgrounds, talents, and skills.OverviewAt Assurex The Reimbursement Specialist 1 coordinates and performs all aspects of billing and collections from Commercial, Government, Private payers in the healthcare industry for AssureRx Health in accordance with training materials, written processes, scripts and Standard Operating Procedures (SOPs). The Reimbursement Specialist 1 works in a high performance, team environment and is responsible for a number of billing and collections-oriented tasks.ResponsibilitiesUnderstand payer requirements for submission of patient claims including appealsPopulate and maintain SOPs, including payer specific data for the management of claims and communicate same to Customer Service.Monitor status of claims in collections systemInvestigate error notifications and hand-off as appropriateRespond to denials, re-submit and/or appeal as appropriateMonitor and report standardized metrics on claims status/progress in a timely mannerEstablish contact points/relationships with payers to optimize claims/appeals processEnsure completeness and accuracy of contract database for in-network payersMonitor cash receipts against contracts database, follow up discrepancies as appropriateWhen claim/appeals process exhausted (according to policy) hand-off to Customer Service to initiate collections from patientsQualificationsHigh School Diploma requiredKnowledge of medical billing and collection practices1-3 years of experience working in a Reimbursement Specialist positionsProficient in all Microsoft Office software applications including strong knowledge in Microsoft ExcelKnowledge of basic medical coding and third-party operating procedures and practicesSkill in answering a telephone in a pleasant and helpful mannerAbility to read, understand and follow oral and written instructionsAbility to establish and maintain effective working relationships with payersMust be well organized and detail-orientedGood financial acumenStrong team skillsExcellent time management, scheduling, and organizational skillsMust be analytical, flexible, innovation, and self-motivatedMust have the flexibility to work extra hours to meet corporate and departmental goalsAbout Our CompanyAssurex is a personalized medicine company that specializes in pharmacogenomics and is dedicated to helping healthcare providers get the genetic information they need to determine the genetically appropriate medication(s) for individual patients suffering from neuropsychiatric and other medical conditions. Assurex Health's proprietary technology is based on pharmacogenomics- the study of the genetic factors that influence an individual's response to drug treatments-as well as evidence-based medicine and clinical pharmacology. The GeneSight test was developed in the Assurex Health clinical laboratory and is based on patented technology licensed from two world renowned medical centers, Mayo Clinic and Cincinnati Children's Hospital Medical Center, who continue to be research collaborators. The company was founded in 2006 and is located in Mason, OH. Assurex Health is a subsidiary of Myriad Genetics, Inc.PI103926247

Integrated DNA TechnologiesID 2018-3995Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 10 hours agoShift/Schedule MTWThF 7:00A-4:00P (United States of America)Overview The Lab Assistant performs preparatory work and general laboratory upkeep to aid in the production of oligonucleotides. ResponsibilitiesEssential Functions:Performs lab cleaning, includes but is not limited to: surface decontamination, equipment decontamination, washing glassware.Stores and organizes lab equipment in the proper manner.Keeps the lab's raw material inventory at appropriate levels.Maintains electronic recordsPerforms administrative tasksDemonstrates behavior consistent with the Integrated DNA Technologies Core Values.Performs other duties as assigned

Tradebe Environmental Services, LLCJob ID 2018-3601# Positions 1Location US-PA-ChambersburgCategory Technical Field Services - Field ChemistsLocation: Company Tradebe Treatment and Recycling, LLCOverviewTradebe is one of the largest global companies in the environmental sector serving various markets including industrial, manufacturing, petrochemical, pharmaceutical, oil & gas and more. As a global business dedicated to sustainable waste management, we seek the greenest waste solutions possible with a priority on recycling and recovery. We recycle over 60% of the waste we process. Our patented SDS technology offers generators an effective, cost-efficient method for recycling organic solid waste to recover viable products as an alternative to waste disposal. Tradebe's network of 24 locations throughout the US includes fully permitted TSDFs and regional 10-day service centers positioned throughout the country. We maintain a fully permitted transportation fleet operating throughout this network to service our clients' diverse transport requirements. For eligible employees we offer health and wellness benefits, including medical, dental, vision, life insurance, 401K, tuition reimbursement, paid time off, and much more. ResponsibilitiesTechnical Services Chemists are the front-line employees who are responsible for the collection, identification, packaging and transportation of hazardous and non-hazardous waste. Our Technical Services Chemists have the opportunity to work directly in the field with clients in university, R&D, manufacturing and healthcare settings, gaining invaluable experience and networking opportunities. The position is aimed at intelligent, hard-working, dedicated, and ambitious people looking to become involved in the environmental services industry and are committed to environmental sustainability. This position requires extensive travel and field work. Responsibilities and Duties:With health and safety as a priority, the selected candidate will need to identify, segregate, and package unused / discarded chemicals produced at our customer locations per DOT and EPA standards. Will label and load containers onto the trucks to transport packaged materials from the customer site to Tradebe facilities within region. Must accurately maintain daily logs, including time sheets, expense reports, dispatch trip reports and vehicle inspection reports. The selected candidate will work directly with clients to answer questions, solve problems and follow all indicated SOPs for the applicable client locations. Must also be able to adhere to all OSHA and Tradebe safety policies. QualificationsA Bachelor's Degree in chemistry, environmental science, or other related science is preferred. Lab Pack experience is preferred but not required. A willingness to travel overnight throughout the week is required. Must have a clean driving record and the ability to obtain a CDL Class B with Hazmat and Tanker endorsements within 6 months of hire. The selected candidate must have successful completion of DOT/OSHA physical exam; have the ability to wear a full-face respirator as well as pass a pre-employment physical, drug screen, and background check. EOE/M/F/Vets/DisabledPI103791460

The Clinical Programming Manager is responsible for the management of all SAS programming project activities within Clinical Programming group.Provides analysis programming including generating reports, tables, listings, graphs, statistical analyses, and applications to satisfactorily fulfill requirements. While some programming is maintenance programming (modifying existing programs), the majority is writing new programs.Contributes to design of program templates. Works with team members to develops new subroutines or expands program to simplify statement, programming, or coding of future problems.Evaluates project progress and recommends changes in procedures and objectivesRepresents group in providing solutions to technical problems.Coordinates validation of all analyses generated by Analysis Programming GroupCollaborates with other function managers and Otsuka departments (i.e., Safety, Medical Writing, Clinical, Biostatistics and Quality Management) to ensure that their requirements are satisfactorily fulfilledDevelops Clinical Programming group training manuals to promote standard processes and procedures.

Integrated DNA TechnologiesID 2018-3978Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 11 hours agoShift/Schedule MTWThF 5:00A-2:00P (United States of America)Overview 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:Gathers, interprets and analyzes scale readouts and BCMS scripts.Participates in the Hazardous Material Spill Response Team.

ResponsibilitiesSenior Manager Data Scientist with expertise in machine learning, artificial intelligence, statistical data analytics, and applications. Must have an excellent knowledge of advanced methods, and experience in applying those methods to a variety of applications. Must be agile to grow in new directions, work with a team of scientists and practitioners from different functional areas to solve problems in pharmaceuticals.Key Job ResponsibilitiesEstablish and implement end to end proof of concept for data analyses across functional areasCreate innovative methodologies for dataBuild proof of concept systemsEstablish strategic partnerships with technical leadership across functional areasPresenting to senior leadership as well external audienceDemonstrates the ability to create new and different solutions that align to real work problems and opportunitiesProficiency in computer programming with excellent software development skills using state-of-the-art technologies and languages (C++, Java, R, Python, and other scripting languages)Required Qualifications:3-5 years hands on experience in machine learningMaster's Degree required and PhD strongly preferred in Computer Science, Statistics, or a related field with focus on data analysisCommand of principles of machine learning, statistical analysis, data mining algorithms, and mathematical modelingDemonstrated ability to use knowledge of recent techniques, and develop new methodologiesDemonstrated experience in applying Machine Learning to at least one of the areas: Computer Vision, Natural Language Analysis or text analysis, large data sets, and social network analysisExcellent software development skills, esp. in rapid prototypingEstablished publication recordExcellent communication skillsExperience in machine learning on large size data using MapReduce and Hadoop preferredExperience in health care data analytics preferredBackground in information security and privacy preferredTravel (approximately 15%)Otsuka Pharmaceutical Company is a global healthcare company with the corporate philosophy: "Otsuka-people creating new products for better health worldwide." Otsuka researches, develops, manufactures and markets innovative products, with a focus on pharmaceutical products to meet unmet medical needs and nutraceutical products for the maintenance of everyday health.In pharmaceuticals, Otsuka is a leader in the challenging area of mental health and also has research programs on several under-addressed diseases including tuberculosis, a significant global public health issue. These commitments illustrate how Otsuka is a "big venture" company at heart, applying a youthful spirit of creativity in everything it does.Otsuka Pharmaceutical Company is a subsidiary of Otsuka Holdings Co., Ltd. headquartered in Tokyo, Japan. The Otsuka group of companies employed 45,000 people worldwide and had consolidated sales of approximately USD 11 billion ( 9.9 billion) in 2016. All Otsuka stories start by taking the road less travelled. Learn more about Otsuka Pharmaceutical Company on its global website at www.otsuka.co.jp/en. Learn more about Otsuka in the U.S. at www.otsuka-us.com.Disclaimer:This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.PI103757377

Responsibilities:The Clinical Data Scientist at Otsuka will support a diverse array of initiatives including advanced computational modeling, clinical development (with particular focus on digital programs), and software development projects. Paramount to this role is the ability to support clinical programs with appropriate analytical strategies.Work closely with stakeholders interfacing with clinical and real-world data to identify, enhance, and support the quantitative and technological needs for all Otsuka projectsManaging software development projects at various levelsReviewing/planning clinical studies across multiple CNS programs, and conducting analyses related to time series modeling, supervised and unsupervised learning techniques, Bayesian methodologies, and othersProvide statistical and modeling support for planning and implementing clinical and real-world evidence studies/programs to meet the value/evidence needs of payers, health systems, clinicians, and patients.Provide solutions of clinical and economic utility by leveraging internal, external and real-world data sources.Guide evidence-based product development (digital/non-digital) by extracting therapeutic intelligence from such data sourcesTravel (up to 15-20%) Qualifications:Qualifications Required:A PhD in Pharmaceutical Science, Statistics, Engineering, Mathematics, or a related quantitative field with 0- 5 of years of post-graduate experienceKnowledge of existing and upcoming statistical methods (supervised and unsupervised) in pharmaceutical data analysisProficiency with programming in software such as Python, R, MATLAB, SAS, SQL etc.Knowledge of pharmaceutical modeling tools such as NONMEM, Monolix, Phoenix NMLE, etc.Knowledge of clinical development and clinical trial executionMust be agile to grow in new directions, acquire new skills, and work with a team of scientists and practitioners from different functional areas to solve problems and create solutions of clinical and economic utility.Must be able to bring insights to stakeholders with ability to extract therapeutic intelligence by leveraging internal, external, and real-world data sources.Excellent communication skillsPreferred:Knowledge of, and experience with, real world databasesKnowledge of current and emerging 'big data' technologiesOtsuka Pharmaceutical Company is a global healthcare company with the corporate philosophy: "Otsuka-people creating new products for better health worldwide." Otsuka researches, develops, manufactures and markets innovative products, with a focus on pharmaceutical products to meet unmet medical needs and nutraceutical products for the maintenance of everyday health.In pharmaceuticals, Otsuka is a leader in the challenging area of mental health and also has research programs on several under-addressed diseases including tuberculosis, a significant global public health issue. These commitments illustrate how Otsuka is a "big venture" company at heart, applying a youthful spirit of creativity in everything it does.Otsuka Pharmaceutical Company is a subsidiary of Otsuka Holdings Co., Ltd. headquartered in Tokyo, Japan. The Otsuka group of companies employed 45,000 people worldwide and had consolidated sales of approximately USD 11 billion ( 9.9 billion) in 2016. All Otsuka stories start by taking the road less travelled. Learn more about Otsuka Pharmaceutical Company on its global website at www.otsuka.co.jp/en. Learn more about Otsuka in the U.S. at www.otsuka-us.com.PI103238316

Integrated DNA TechnologiesID 2018-3969Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 9 hours agoShift/Schedule M-F 40 Hour Week (United States of America)Overview The Chemical Process Development Scientist develops raw material manufacturing processes, oligonucleotide manufacturing processes and coordinates change control of those processes.ResponsibilitiesEssential Functions:Designs and performs experimentation with assistance or as prescribed by management to improve existing or create new processes or materials.Manages new processes from proof of concept through validation and implementation. Prioritizes work and completes projects in an accurate and timely manner. Analyzes and interprets QC and experimental data.Collaborates and effectively communicates with all levels of IDT staff within various departments to facilitate successful project and process outcomes, including full documentation via reports and/or presentations.Documents all testing via reports and/or presentations and presents data and recommend future steps.Manages all aspects of internal and external process and technology transfers.Adheres to all departmental protocols, rules, and safety regulations and understand the requirements of ISO 9001, ISO 13485, and ISO 14001.Programs, uses and maintains equipment.Prepares reports and presentations to communicate data and make recommendations for further action.Drives change at all IDT locations.Demonstrates behavior consistent with the Integrated DNA Technologies Core Values.Performs other duties as assigned.

Integrated DNA TechnologiesID 2018-3965Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 18 hours agoShift/Schedule MTWThF 7:00A-4:00P (United States of America)Overview The Formulation Scientist I formulates custom oligonucleotides according to the customer's specifications. This generally includes quantification, final packaging, and QC sampling of the products being made.ResponsibilitiesJob Specific Essential Functions:Uses automated and manual lab equipment accurately; including limited maintenance and troubleshooting activitiesUses custom software packages to complete tasks and create final productUtilizes stoichiometry to convert measurement units and creates custom solutionsTranslates order requirements into a process to formulate oligos to the customer's specificationsQuantifies and samples oligos for quality control testsAssesses QC data accurately and makes pass/fail decisions for oligosMaintains daily ship deadlines for all productsMaximizes automation for all processesIncorporates new products and processes continuouslyAdheres to safety regulations, lab SOPs, and contamination controlsDemonstrates behavior consistent with the Integrated DNA Technologies Core ValuesPerforms other duties as assignedPosition Specific Essential Functions:Completes replication of plate and/or tube ordersUtilizes ERP system to order lab supplies and fulfill work orders, as neededAssists with writing and double checking scripts and mapping for liquid handlersAssists with creating and following custom flows for special processing ordersCompletes backend checks on final product, as required

Integrated DNA TechnologiesID 2018-3967Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 14 hours agoShift/Schedule MTWTh 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 techniquesAdheres to safety regulations, lab SOPs, and contamination controlsUses lab equipment including limited maintenance and troubleshooting activitiesUses custom software packages to complete tasks and create final productAssesses QC data accurately and makes pass/fail decisions for oligosHandles expensive oligos and reagentsKeeps thorough records of specialized processes in the oligo process historyFollows documented custom instructions, when applicableDemonstrates behavior consistent with the Integrated DNA Technologies Core ValuesPerforms other duties as assignedPosition Specific Essential Functions:Organizes and handles customer owned materials as well as non-standard reagent formulationsPrepares oligos for final shipment to customer or for further processing in other departmentsUses aids and SOPs to make decisions about the proper production path per product

Integrated DNA TechnologiesID 2018-3913Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 8 hours agoShift/Schedule MTWTh 8:30P-7:30A (United States of America)Overview The Formulation Scientist I formulates custom oligonucleotides according to the customer's specifications. This generally includes quantification, final packaging, and QC sampling of the products being made.ResponsibilitiesPosition Specific Essential Functions:Completes replication of plate and/or tube orders Utilizes ERP system to order lab supplies and fulfill work orders, as neededAssists with writing and double checking scripts and mapping for liquid handlersAssists with creating and following custom flows for special processing ordersCompletes backend checks on final product, as requiredJob Specific Essential Functions:Uses automated and manual lab equipment accurately; including limited maintenance and troubleshooting activitiesUses custom software packages to complete tasks and create final productUtilizes stoichiometry to convert measurement units and creates custom solutionsTranslates order requirements into a process to formulate oligos to the customer's specificationsQuantifies and samples oligos for quality control testsAssesses QC data accurately and makes pass/fail decisions for oligosMaintains daily ship deadlines for all productsMaximizes automation for all processesIncorporates new products and processes continuouslyAdheres to safety regulations, lab SOPs, and contamination controlsDemonstrates behavior consistent with the Integrated DNA Technologies Core ValuesPerforms other duties as assigned

Environmental Analyst I - Geologist Stony Brook, NY The New England Interstate Water Pollution Control Commission (NEIWPCC) and the New York State Department of Environmental Conservation (NYSDEC) are seeking an organized and diplomatic Environmental Analyst – Geologist to provide overall program implementation on Long Island, update Source Water Assessment and Protection Plans (SWAPPs), and provide technical assistance to communities preparing SWAPPs. Candidate will review and prioritize existing SWAPPs for Nassau and Suffolk Counties and coordinate with NYSDEC and other state and local agencies to collect relevant information. Will identify potential contamination threats from geothermal systems, Hazardous Waste Remediation sites, inactive landfills, petroleum spill sites, threats from industrial and commercial facilities, solid waste facilities, and areas with 1,4-dioxane and PFAS contamination.

Integrated DNA TechnologiesID 2018-3911Job Locations US-CA-San DiegoCategory Manufacturing Operations# of Openings 1Posted Date 12 hours agoShift/Schedule M-Th 2-11p and F 1-10pOverview The Team Leader provides guidance and direction for the department by ensuring that workflow is prioritized and that processes are being followed according to protocol. This position acts as a resource to personnel and as a liaison between management and staff. ResponsibilitiesJob Specific Essential Functions:Assists with supervising and directing staff which would include employee hiring, training, evaluations and discipline. Organizes and prioritizes workflow within the group and communicates with staff to ensure that all products are completed, according to customer requirements, and sent to shipping department in a timely manner. Performs all responsibilities of a Production Scientist I and II.Collaborates with other critical operational departments to ensure product completion, according to customer specifications.Interprets QC results and follows up when failures warrant further investigation.Troubleshoots instrument problems encountered and submits/tracks work orders when necessary.Troubleshoots and corrects problems that may arise throughout the process.Uses aids and SOPs to make decisions about the proper production path per product.Keeps all work instructions and logs current pertaining to processes, and initiates the creation of additional documents when necessary.Communicates group needs to management regarding potential quality, speed or cost improvementsDemonstrates and upholds behavior consistent with the Integrated DNA Technologies Core Values and delivers the Integrated DNA Technologies experience to customers and other business associates.Performs other duties as assigned.

Clemson University: College of Engineering, Computing and Applied SciencesWarren H. Owen Distinguished Professor in Electrical & Computer Engineering with a focus in Power Electronics and DrivesLocation: Riggs HallApplications and nominations are sought for the Warren H. Owen Distinguished Professor in Electrical and Computer Engineering at Clemson University (http://www.clemson.edu/ece/). The candidate's teaching and research should encompass a broad range of topics related to power electronics, including power electronic devices, converter topologies, control, electrical drive systems and energy storage systems. In addition, the ideal candidate should have a solid understanding of the cyber-infrastructure related areas of power electronic systems such as embedded controller systems, networking, and communication and sensing. The person filling the position will hold a senior faculty position in the Holcombe Department of Electrical and Computer Engineering and will be located on Clemson's main campus in Clemson, SC. The Holcombe Department of Electrical and Computer Engineering is one of the largest and most active departments at Clemson, withover 35 primaryfaculty positions and 14 affiliated full-time faculty members, approximately 550 undergraduates and 190 graduate students. The main campus includes state-of-the-art real-time simulation facilities for research in intelligent control of the electric grid, a modern power-electronics laboratory, and a thriving undergraduate and graduate emphasis in power systems. There are also power system facilities at the Clemson University Restoration Institute (CURI) in N. Charleston SC, that are associated with the department. CURI houses a $98M power facility initiated in 2009 from a $45M Department of Energy grant. The facility includes the SCE&G Energy Innovation Center which contains the world's most-advanced wind-turbine drivetrain testing facility capable of full-scale highly accelerated mechanical and electrical testing of advanced drivetrain systems for wind turbines. The SCE&G Energy Innovation Center also houses the Duke Energy Electrical Grid Research Innovation and Development (eGRID) Center, a facility with real-time simulation and 20MVA hardware-in-the-loop capability. Clemson University is the largest land-grant institution in South Carolina, enrolling 18,600 undergraduates and 4,800 graduate students. Seven colleges house strong programs in architecture, engineering, science, agriculture, business, social sciences, arts and education. A faculty of 1,500 and staff of 3,700 support 84 undergraduate degree offerings, 73 master's degree programs and 40 Ph.D. programs. An annual operating budget of approximately $1.1.5 billion and an endowment of $683 million fund programs and operations. The University has externally funded research expenditures of $109 million per year. Research and economic development activities are enhanced by public-private partnerships at 4 innovation campuses and 6 research and education centers located throughout South Carolina. Clemson University is ranked 23rd among national public universities by U.S. News & World Report.QUALIFICATIONSApplicants must have an earned doctorate in Electrical Engineering or a closely related field.APPLICATION INSTRUCTIONSTo apply, please submit a cover letter, a CV, the contact information for *five* references, a research statement, and a teaching statement via Interfolio. To ensure full consideration, applicants must apply by November 15, 2018; however, the search will remain open until the position is filled.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.PI103612858

Territory: Southwest (preferred location is in the central part of the USA near a large metro area) Responsibilities: To be a credible source of evidence based information that demonstrates the value of Otsuka products from the clinical, economic and humanistic standpoint and works in partnership with providers, payers and other key stakeholders to apply practical real-world solutions to improve patient outcomes. This position will cover cross-therapeutic areas within the company.Insights: collect and submit field medical insights that drive decision making and prioritization of evidence generation efforts and healthcare solutionsSolutions: identify opportunities for solutions within territory that improve patient outcomes; deploy and apply solutions through direct customer interactionsHealthcare Systems & Trends: maintain a comprehensive knowledge of territory, the interconnectivity of the key decision makers within and the challenges faced in providing and delivering optimal patient careEconomic Value: communicate and deliver pharmacoeconomic data (including quality, cost and patient outcomes) that address payer and provider needs and priorities; including implementing practice decision support and care management tools that positively impact the delivery of patient careCompliance: conduct all interactions with healthcare professionals, payers and other stakeholders in accordance with all applicable Otsuka policies and procedures.Qualifications:Advanced degree in Pharmacy, Medicine, Biological Sciences, Health Services Research or Public Health, (Pharm.D., M.D., Ph.D. or D.Ph.) is requiredMust have an understanding of the interconnectivity of health systems, overall delivery of patient care and how to solution with the overall goal of improved patient outcomesMust be an expert on current literature, therapeutic issues, process of care and the competitive landscape related to therapeutic areaWillingness to travel (60-80% travel time) within assigned territoryOtsuka Pharmaceutical Development & Commercialization, Inc. (OPDC) is an innovative, fast-growing healthcare company that discovers and develops new compounds that address unanswered medical needs and advance human health. With a strong focus on neuroscience, oncology, and cardio-renal treatments, OPDC is dedicated to improving the health and quality of human life. For more information, visit www.otsuka-us.com. OPDC is a subsidiary of Otsuka America, Inc. (OAI), a holding company established in the U.S. in 1989. OAI is wholly owned by Otsuka Pharmaceutical Co., Ltd. The Otsuka Group employs approximately 42,000 people globally and its products are available in more than 80 countries worldwide. Otsuka welcomes you to visit its global website at https://www.otsuka.co.jp/en/.Disclaimer: This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.PI103522983

Integrated DNA TechnologiesID 2018-3950Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 10 hours agoShift/Schedule PT 10-19 hours/week (United States of America)Overview The Lab Assistant performs preparatory work and general laboratory upkeep to aid in the production of oligonucleotides. ResponsibilitiesJob Specific Essential Functions:Performs lab cleaning, includes but is not limited to: surface decontamination, equipment decontamination, washing glassware.Stores and organizes lab equipment in the proper manner.Prepares tubes, plates and other labware for use as necessaryMaintains electronic records of tasks performedPerforms administrative tasksComplies with the requirements for an ISO 9001 and ISSO 14001 environment.Performs necessary safety, emergency, and cleaning procedures.Demonstrates behavior consistent with the Integrated DNA Technologies Core ValuesPerforms other duties as assignedPosition Specific Essential Functions:Crushes glass when necessaryApplies proper expiration dating to reagent/cleaning labelsAdheres to safety regulations, lab SOPs, and contamination controlsPerforms tasks outlined by the Maintenance Connection schedule within the given time period

Clemson University: College of Science: Biological SciencesProfessor- Organismal BiologyLocation: Long 132The Department of Biological Sciences at Clemson University invites applications for three tenure-track Assistant Professor positions in (1) Microbiology, (2) Evolutionary Medicine, and (3) Organismal Biology, with an expected start date of August, 2019. We seek creative, interactive individuals who address cutting-edge research questions. The Department awards undergraduate and graduate degrees in Biological Sciences and Microbiology, as well as graduate degrees in Environmental Toxicology. The department of Biological Sciences is a founding member of the newly formed College of Science, a central player in both the university's strategic plan, ClemsonForward (https://www.clemson.edu/forward/) and the college's ScienceForward plan (https://www.clemson.edu/science/about/scienceforward.html). We invite applicants who will complement and enhance the Department's existing research strengths (http://www.clemson.edu/science/departments/biosc/). Located on Lake Hartwell in the foothills of the Blue Ridge Mountains, Clemson University is South Carolina's public land-grant University. As a Carnegie R1 Institution, the University has excellent research resources including the globally ranked Palmetto high performance computing cluster, Sciences Genomics and Bioinformatics Facility, state-of-the-art light microscopy, electron microscopy, animal, or fish facilities, a multi-user analytical laboratory and metabolomics core, the Campbell Museum of Natural History, and the 17,500-acre Clemson Experimental Forest. There are many opportunities for collaboration across a wide group of partners on and off campus, including faculty in other departments in the College of Science, the College of Engineering, Computing and Applied Sciences, or other colleges at Clemson, USC School of Medicine in Greenville, Greenville Health System, and the Center for Human Genetics (Greenwood, SC). The University and Department are committed to building a diverse and inclusive body of faculty scholars dedicated to working and teaching in a multi-cultural environment (http://www.clemson.edu/inclusion/). We encourage applications from women, minorities, and individuals with a commitment to mentoring underrepresented demographics in the sciences. We are also supportive of the needs of dual career couples. Successful candidates must hold a doctoral degree and have postdoctoral experience. Competitive candidates will demonstrate an ability to develop a vigorous and independent, externally funded and nationally recognized research program; demonstrate teaching excellence and a commitment to diversity inclusion; and participate in relevant undergraduate and graduate education programs.We seek an organismal biologist using integrative and/or comparative approaches to examine fundamental biological questions. We especially encourage applicants whose work integrates across scales and utilizes big data approaches to understand biodiversity and processes of change.QUALIFICATIONSSuccessful candidates must hold a doctoral degree and have postdoctoral experience. Competitive candidates will demonstrate an ability to develop a vigorous and independent, externally funded and nationally recognized research program; demonstrate teaching excellence and a commitment to diversity inclusion; and participate in relevant undergraduate and graduate education programs.APPLICATION INSTRUCTIONSApplicants should submit the following items to the distinct Interfolio link listed for the position to which they apply: (1) letter of application; (2) CV; (3) statement of research interests and future plans; (4) statement of teaching interests and experience; (5) statement describing past experience and/or future plans to promote diversity and inclusion; and (6) up to three reprints in one PDF. Applicants should also arrange, through Interfolio, for three confidential letters of recommendation to be submitted. For full consideration, applications should be submitted by August 31, 2018. Review will continue until the positions are filled.Inquiries should be directed to Dr. Christopher L. Parkinson (viper@clemson.edu).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.PI103487784