89 jobs found

ChobaniChobani is an equal opportunity employer. Chobani will not discriminate against any applicant for employment on any basis including, but not limited to: race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, marital status, predisposing genetic characteristics and genetic information, or any other classification protected by federal, state and local laws.Location: Twin Falls, IdahoCategory: Research & DevelopmentWe are seeking a Principal Scientist, with an emphasis on nutrition, with a track record of research excellence and food discovery experience to join our R&D team. Expertise in nutritional science is required. The ideal candidate will be a highly motivated individual - skilled at working on multiple projects concurrently. They will have broad responsibilities and opportunities for growth in a collaborative work environment. Knowledge of recent scientific advances and the ability to translate these into research directions is important. As part of the Chobani team, you will be responsible for advancing projects in the discovery pipeline and conducting hypothesis-driven research that complement our programs.The responsibilities of this position include:Execute research and development plans and strategies for nutritional development in support of company objectives - this includes on cost and on time deliveryManage projects developing new formulations and products from conceptualization to commercializationProactively support the project teams, providing nutritional insight and strategic advice to ensure the feasibility and success of product development initiativesProvide ideas/concepts for constructing the product pipeline (e.g. new products, new combinations, new technologies)Communicate project requirements and recommendations as well as status to internal customers and external vendorsPromote more efficient and effective collaborative project workLead, assist, and work directly with plant processing and production personnel to ensure trial runs and start-up operations are performed on time and on costAble to conduct hands on analytical testing of nutrition and able to train scientists and technicians on basic physical, chemical and rheological testing required for the productBuild and develop an active collaboration with academia and external partners to grow the scientific collaboration with ChobaniAble to design and execute complex Design of Experiments, data collection and statistical data analysis on projects and train scientists and technicians on the sameAssist with design of pilot and industrial plant based on proven processSupport ideation, substantiation, and defense of claims, as well as challenges against competitors' claimsFollow Chobani's safety procedures and Good Manufacturing PracticesThe requirements of this position include:Minimum M.S in Nutritional Science or related degree. Advanced degree strongly preferred.3-5 years of relevant food industry experience, depending on level of degreeAbility to collect, analyze and present dataCapable of designing and executing research programsStrong people, influencing and relationship skills built in a complex environment Strong statistical training and ability to translate scientific learnings into simple communicationMaintain clean & safe manufacturing environment within all facilitiesExcellent written and verbal communicationFirm understanding of product and process developmentBusiness and product knowledgeMust be a self-starterFlexibility to travel/work across locations and time zones up to 50% of the timeAbout Us:Since our founding 10 years ago, we've always been a different kind of company. After moving to New York from his native Turkey, our CEO Hamdi Ulukaya found that in America, yogurt just wasn't as delicious or widely available as it was back home. He thought everyone deserved better options, so he set about making delicious, nutritious, natural, and accessible Greek Yogurt right here in the U.S.Our mission since day one has been to provide better food to more people. And now as the No. 1-selling Greek Yogurt brand in America and the second largest overall yogurt manufacturer, we believe every food maker has a responsibility to provide people with better options, which is why we're so proud of the way our food is made.Our food philosophy of crafting quality products with simple ingredients is what makes Chobani a different kind of yogurt. Our belief that business done right has the ability to change lives and strengthen communities is what makes Chobani a different kind of company. From the way we source our ingredients to how we treat our employees, Chobani strives to make universal wellness happen sooner with everything we do. Certified as a Great Place to Work ® for the last two years, our culture is built on shared passion, dedication, and a commitment to doing what is right. Together, the Chobani family has created something unlike what any company has done before. The possibilities are endless.PI107906470

Seattle GeneticsSeattle Genetics is an equal opportunity employer. All qualified applications will receive consideration for employment without regard to race, age, gender identity, sexual orientation, color, religion, sex, marital status, national origin, protected veteran status, disability status, or any other status protected by federal, state, or local law.Process Sciences . Bothell, WashingtonDescription Summary: The Analytical Sciences department is seeking a highly motivated and innovative Scientist/Sr. Scientist with prior biotechnology experience to join our team. The position will interact closely with the discovery research organization and be part of a team responsible for evaluating candidate manufacturability and charting a roadmap to continuously improve capabilities in the prediction, characterization, and control of the molecular liabilities that may limit development speed. The position will also be responsible for providing technical leadership in support of development, qualification and troubleshooting methods spanning various analytical platforms including chromatography and capillary electrophoresis. The successful candidate will actively participate in efforts directed at improving process efficiencies, expanding the range of assays and applications and improving technologies and infrastructure, from conceptualizing to experimental design through implementation. Responsibilities: Plan and execute analytical developability assessments and collaborate with colleagues in discovery research, protein engineering, process sciences and project management during the research to development transitionRepresent analytical sciences in highly collaborative groups across process sciences, manufacturing and researchContribute to the implementation of technologies and strategies aimed at successful and rapid development of novel biotherapeutic modalities Assist junior colleagues with sample analysis, troubleshooting, and instrument preventative maintenanceContribute to early and late phase pipeline programs through development, qualification, and transfer of analytical test methodPerform product characterization and analytical comparability exercises on diverse pipeline of biotherapeutics Author and review of analytical technical reports, IND and BLA filings Qualifications: PhD in life sciences field with 2+ years working experience in pharmaceutical or biotech field. BS or MS in life science field with 8+ years (MS) or 10+ years (BS) experience in pharmaceutical or biotech field. Prior experience in research and/or development of recombinant human protein therapeutics preferredStrong working knowledge of fundamental biopharmaceutical principles including an understanding of protein structure, chemistry, and degradation mechanismsPractical experience with biochemical and biophysical characterization methods such as chromatography, electrophoresis, UV/CD/fluorescence spectroscopies, calorimetry, light scattering, and sedimentation is preferred Good work ethic, team- and project-focused, and motivated to produce high quality data on aggressive timelinesExcellent written and oral communication skills, organization, multitasking, and demonstrated success working in a collaborative cross-functional environment As the leading employer in our industry in the Pacific Northwest, Seattle Genetics is proud to offer a competitive total compensation package as well as a comprehensive benefits program designed to support the whole lives of our employees and their families. Benefits include medical, vision and dental coverage, group and supplemental life insurance, 401(k) with company match, tuition reimbursement, relocation assistance and much more. To learn more about Seattle Genetics, please visit www.seattlegenetics.com.PI107876253

Integrated DNA TechnologiesID 2019-4530Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 14 hours agoShift/Schedule PT 20-29 hours (Saturdays 2pm-11pm and Sunday noon-4pm)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:Prepares columns and tubes and pours gels for the purification process.Crushes glass when necessaryAdheres to safety regulations, lab SOPs, and contamination controlsPerforms tasks outlined by the Maintenance Connection schedule within the given time period

Pharmaceutical Research Associates, Inc.(All) | US-RemoteOverview Do you want to watch clinical development change, or do you want to be the one to shape it?Because we're hoping you're here for the latter.Who are we?We Are PRA.We are 15,000+ employees strong, operating in more than 85 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most. Who are you?You are an innovative, analytical problem solver. You enjoy working with data and digging deeper to uncover answers. Clear, concise communication is the name of the game for you. It's how you get things done. You are energized through interactions with clients and team members and you know how to rally the troops to accomplish big things together.You are an experienced statistician who has worked within multiple statistical and therapeutic areas. You not only know how to plan, implement, and monitor the statistical processes for multiple clinical studies, but you're comfortable leading these initiatives. You're used to people coming to you for advice and you find it rewarding to watch your mentees succeed and grow. Because you're passionate about the work you do and the contributions you make, those around you feel inspired to do more!Still with us? Great! Because if this sounds like you, we want to learn more!Responsibilities What will you be doing?As a Senior Biostatistician, you are the lead on project teams for simple to complex clinical studies. You develop statistical analysis plans and reporting specifications for complex studies. You perform statistical analysis and interpret results. You perform the senior review of TFLs and provide significant input in the development and review of CRFs, edit specifications, and critical variable lists. You contribute to clinical study protocols and clinical study reports. As a Senior Biostatistician, you are responsible for training and mentoring new or junior statisticians on statistical methods and PRA procedures.Qualifications What do you need to have?• Master's degree in statistics or biostatistics.• At least 5 years of biostatistics experience.• Strong knowledge of multiple statistical and therapeutic areas, the drug development process, SAS procedures, and good programming practices. Oncology experience is desired, but not required. • Demonstrated ability to plan, implement, and monitor the statistical processes for multiple clinical studies. • Excellent communication skills and leadership ability. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.PI107867270

Princeton UniversityRequisition # 2019-9949Department PPPL NSTXCategory Research and LaboratoryFull-Time / Part-Time Full-TimeOverview The Princeton Plasma Physics Laboratory seeks to fill a staff Research Physicist position to work on energetic particle diagnostics and on the physics of energetic particle driven instabilities on the NSTX -U Spherical Torus. The main focus is to contribute to the development and operation of fast ion diagnostics that are essential to the operations of NSTX-U, as well as to conduct experimental research on NSTX-U to develop improved understanding of energetic particle transport mechanisms in tokamaks, with a specific focus on compact Spherical Torus configurations.Responsibilities The successful candidate will be responsible for upgrading and maintaining fast ion diagnostics on NSTX-U. In addition, the successful candidate will be responsible for the upgrade and operation of neutron detectors on NSTX-U during both the preparation for operations phase as well as during physics operation. The candidate will also interact with physicists working on energetic particle physics at PPPL to contribute to the validation of models for fast ion driven instabilities and their effect on fast ion transport against data from the NSTX-U fast ion and fluctuation diagnostics.Qualifications We are looking for a highly motivated, experienced scientist with good knowledge of energetic particle physics who will collaborate closely with both theorists and experimentalists. Applicants should have demonstrated skills in designing and operating fast ion diagnostics on tokamaks. Previous experience with first-principles numerical codes for simulations of fast ion physics in tokamak geometry is highly desirable. Preference will be given to candidates with proven experience in experimental plasma physics and knowledge in using & interpreting results from numerical codes, including first-principles codes for fast ion physics and more general tokamak transport codes such as TRANSP. Applicants should possess a Ph.D. in plasma physics and at least 3 years of experience as Research Scientist or equivalent. The position is at the RM2 level. For information: Mario Podest, email: mpodesta@pppl.govPrinceton University is an Equal Opportunity/Affirmative Action Employer and all qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, or any other characteristic protected by law. EEO IS THE LAW Salary Grade RES, 02 Standard Weekly Hours 40.00 Eligible for Overtime No Benefits Eligible Yes Essential Services Personnel (see policy for detail) No Physical Capacity Exam Required No Valid Driver's License Required No Connect With Us!Connect With Us! Join our Talent Network to receive updates about working at Princeton. If you are a qualified individual with a disability and are, therefore, unable or limited in your ability to use or access this system, you can request a reasonable accommodation by calling a Human Resources team member at (609) 243-2200. Princeton University/Princeton Plasma Physics Laboratory is an Equal Opportunity/Affirmative Action Employer and all qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, or any other characteristic protected by law. EEO IS THE LAW Princeton University/Princeton Plasma Physics Laboratory job offers are contingent upon the candidate's successful completion of a background check, reference checks, and pre-employment screening, as applicable. The type and extent of background check, reference checks, and pre-employment screening may vary depending on the requirements and/or functions of the job and the candidate's current employment status with Princeton University/Princeton Plasma Physics Laboratory. Princeton University/Princeton Plasma Physics Laboratory is a residential community and an employer that operates continuously 24 hours a day. Essential services employees perform jobs that are necessary and required to maintain basic University operations during scheduled closures or unscheduled suspension of normal operations due to emergencies, events, or other situations. Essential services employees may be asked and/or required to perform jobs or duties that fall outside of their normal job classification during an emergency event. Learn more about our Essential Services policy. If you have questions or comments regarding the iCIMS Privacy Policy or iCIMS FAQs, please contact accounts@icims.com. Go to Princeton University careers site. PI107831150

Integrated DNA TechnologiesID 2019-4562Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 1 day agoShift/Schedule M-F 7:00A-4:00P (United States of America)Overview The Purification Scientist I purifies custom oligonucleotides according to the customer's order. This generally includes the sorting, purification, and QC sampling of the products being made.ResponsibilitiesJob Specific Essential Functions:Adheres to safety regulations, lab SOPs, and contamination controlsPerforms the purification of oligos using various techniquesUses automated and manual lab equipment including limited maintenance and troubleshooting activitiesQuantifies and samples oligos for quality control testsAssesses QC data accurately and makes pass/fail decisions for oligosEnsures that product meets final purity guarantees through the custom purification processSorts oligos for the proper purification either by hand or using softwareUses custom software packages to complete tasks and create final productTroubleshoots oligo failures and makes thoughtful sorting and purification decisionsDemonstrates behavior consistent with the Integrated DNA Technologies Core ValuesPerforms other duties as assignedPosition Specific Essential Functions:Follows process flows including product specific flowsPerforms hand coupling of modificationsPerforms salt exchange precipitations by hand for non-routine process flowFollows protocols to mitigate carryover

Integrated DNA TechnologiesID 2019-4565Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 1 day agoShift/Schedule SuMTWTh 3:00P-12:00A (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 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 required

Integrated DNA TechnologiesID 2019-4566Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 1 day agoShift/Schedule M-F 5:00A-2:00P (United States of America)Overview The Purification Scientist I purifies custom oligonucleotides according to the customer's order. This generally includes the sorting, purification, and QC sampling of the products being made.ResponsibilitiesJob Specific Essential Functions:Adheres to safety regulations, lab SOPs, and contamination controlsPerforms the purification of oligos using various techniquesUses automated and manual lab equipment including limited maintenance and troubleshooting activitiesQuantifies and samples oligos for quality control testsAssesses QC data accurately and makes pass/fail decisions for oligosEnsures that product meets final purity guarantees through the custom purification processSorts oligos for the proper purification either by hand or using softwareUses custom software packages to complete tasks and create final productTroubleshoots oligo failures and makes thoughtful sorting and purification decisionsDemonstrates behavior consistent with the Integrated DNA Technologies Core ValuesPerforms other duties as assignedPosition Specific Essential Functions:Follows process flows including product specific flowsPerforms hand coupling of modificationsPerforms salt exchange precipitations by hand for non-routine process flowFollows protocols to mitigate carryover

Integrated DNA TechnologiesID 2019-4568Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 1 day agoShift/Schedule Su-Th 7:00A-4:00P (United States of America)Overview The Purification Scientist I purifies custom oligonucleotides according to the customer's order. This generally includes the sorting, purification, and QC sampling of the products being made.ResponsibilitiesJob Specific Essential Functions:Adheres to safety regulations, lab SOPs, and contamination controlsPerforms the purification of oligos using various techniquesUses automated and manual lab equipment including limited maintenance and troubleshooting activitiesQuantifies and samples oligos for quality control testsAssesses QC data accurately and makes pass/fail decisions for oligosEnsures that product meets final purity guarantees through the custom purification processSorts oligos for the proper purification either by hand or using softwareUses custom software packages to complete tasks and create final productTroubleshoots oligo failures and makes thoughtful sorting and purification decisionsDemonstrates behavior consistent with the Integrated DNA Technologies Core ValuesPerforms other duties as assignedPosition Specific Essential Functions:Follows process flows including product specific flowsPerforms hand coupling of modificationsPerforms salt exchange precipitations by hand for non-routine process flowFollows protocols to mitigate carryover

Integrated DNA TechnologiesID 2019-4567Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 1 day agoShift/Schedule Tu-F 4:30P-3:30A (United States of America)Overview The Purification Scientist I purifies custom oligonucleotides according to the customer's order. This generally includes the sorting, purification, and QC sampling of the products being made.ResponsibilitiesJob Specific Essential Functions:Adheres to safety regulations, lab SOPs, and contamination controlsPerforms the purification of oligos using various techniquesUses automated and manual lab equipment including limited maintenance and troubleshooting activitiesQuantifies and samples oligos for quality control testsAssesses QC data accurately and makes pass/fail decisions for oligosEnsures that product meets final purity guarantees through the custom purification processSorts oligos for the proper purification either by hand or using softwareUses custom software packages to complete tasks and create final productTroubleshoots oligo failures and makes thoughtful sorting and purification decisionsDemonstrates behavior consistent with the Integrated DNA Technologies Core ValuesPerforms other duties as assignedPosition Specific Essential Functions:Follows process flows including product specific flowsPerforms hand coupling of modificationsPerforms salt exchange precipitations by hand for non-routine process flowFollows protocols to mitigate carryover

IHRC, Inc.IHRC, INC. IS AN EQUAL OPPORTUNITY AND AFFIRMATIVE ACTION EMPLOYER. It is the policy of IHRC, Inc. to provide equal employment opportunities without regard to race, color, religion, citizenship, age, sex, sexual orientation, gender identity, national origin, ancestry, genetic information, veteran or disability status, or any other characteristic protected by applicable federal, state or local law, and to take affirmative action in accordance with applicable laws and Executive Orders.BioinformaticianLocation: GA - AtlantaRefID: ind1DescriptionJOB TITLE: BioinformaticianPOSITION NUMBER: 1902-92032-BI-01POSITION LOCATION: Atlanta, GA, USAANTICIPATED START DATE: Two weeks after candidate identificationTRAVEL: As required to fulfill the responsibilities of the positionIHRC, Inc. provides scientific, information management, management consulting, bioinformatics, and administrative program support to the Centers for Disease Control and Prevention (CDC) and other Federal and private sector clients. The successful candidate will be a full-time employee of IHRC, Inc., and will be assigned to the Meningitis Laboratory, Meningitis and Vaccine Preventable Diseases Branch (MVPDB), Division of Bacterial Diseases (DBD), National Center for Immunization and Respiratory Diseases (NCIRD), at the CDC, 1600 Clifton Road, Atlanta, GA to provide support for the development, enhancement, and maintenance of the laboratory and public health capacity of MVPDB.SCOPE OF WORKThe Bioinformatician will explore, assess and implement proper bioinformatics applications and tools to improve the bioinformatics capacity of the Meningitis Laboratory. Responsibilities will include organization, management and analysis of bioinformatics data obtained from pathogenic isolates collected through surveillance, carriage and other studies, and the development of cutting edge bioinformatics tools to advance the understanding of meningitis epidemiology, transmission, vaccine effectiveness, virulence and bacterial biology.MAJOR DUTIES AND RESPONSIBILITIES Perform quality control, assembly, annotation and analysis of pathogen genome sequences and management of genome sequence files and databases, including uploads to NCBI or other similar sequence data banks Develop, validate and implement suitable and customized whole genome sequencing based applications, data management systems, and cutting edge bioinformatics tools to improve and advance molecular diagnosis of different diseases Utilize existing open source and commercially available software and author custom code to fully analyze NGS data and ensure that all NGS data and metrics meet Quality Management standards Develop and maintain Standard Operating Procedures and protocols for bioinformatics analysis of next generation sequencing data Work with scientists in the laboratory to address public health related scientific questions and develop new systems to improve surveillance Prepare and deliver clear and concise reports and presentations for supervisors, colleagues, and collaborators, at internal and external (scientific) meetings Prepare scientific reports and manuscripts for meetings and publications Effectively communicate technical elements of bioinformatics to other staff scientists and upper management Provide technical support, guidance, advice and consultation for bioinformatics related studies and projects Provide training and assistance to scientists in the use of bioinformatics tools Participate in other laboratory activities as necessary MINIMUM QUALIFICATIONS Education and Experience: Master’s Degree in microbiology, biology, chemistry, computer science, bioinformatics, computational biology, mathematics, or basic medical science Required: Proficiency in the use of various open source and commercially available next generation sequence analysis tools Experience in the assembly, analysis, and annotation of genomic data from a variety of sequencing platforms such as Illumina, 454, PacBio, and IonTorrent Experience preforming phylogenetic analysis Experience performing quality assurance and control procedures on raw sequence reads Experience with Unix (BASH scripting) Experience with programming languages such as Python, Perl, Java, C, C++, JavaScript, SQL and R Experience creating and maintaining NGS databases Exceptional written and oral presentation skills and the ability to effectively convey information Exceptional communication and interpersonal skills, required for working in a fast paced multidisciplinary team environment, and for extensive interaction with clients and external partners Experience working with Microsoft Office, Access, Excel, and PowerPoint Desirable: Experience with relational databases such as MySQL and Microsoft SQL server Expertise in the underlying theory and the application of a wide range of bioinformatics tools Experience developing and implementing genomic typing methods Experience developing bioinformatics pipelines for analysis of NGS data Ability to configure and maintain a Unix/Linux bioinformatics computing environment Demonstrated skills and experience writing project reports, research protocols and manuscripts Demonstrated ability to synthesize new research ideas for project research Language Skills: The candidate must possess excellent oral and written communication skills in English REQUIREMENT: Must be United States citizen or permanent resident or have authorization for employment in the United States SALARY: Commensurate with qualifications and experienceTo apply for this position: If you are viewing this position on the IHRC Career Center, please click on the "Apply Now" button. If you are viewing this position on a site other than the IHRC Career Center, you may use the "click to apply" link, or you may apply by visiting our Career Center and searching for the position number listed at the top of this position description. To view all of our open positions, and to apply to those positions in which you may be interested, please visit our Career Center, which can also be reached by visiting www.ihrc.com/Careers and clicking on the "View Opportunities" link. PI107829825

Amyris, Inc.Location: Emeryville, CATeam: Intern - Process Analytical ChemistryWork Type: InternAmyris, 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.Amyris seeks to hire summer interns for the Process Analytical Chemistry (PAC) group, located in Emeryville, CA. As an Intern in our Process Analytical Chemistry group, you will be a member of a team developing and running analytical methods to test fermentation recovery and purification streams. The Process Analytical Chemistry team works closely with the Separations and Chemical Purification teams, providing data to guide process development. Each intern will work on a project under the mentorship of a scientist. The ideal candidate will be someone with a strong interest in biotechnology and analytical chemistry desiring hands on experience with a variety of cutting-edge instrumentation such as mass spectrometry, gas chromatography, high pressure liquid chromatography and ion chromatography.ResponsibilitiesFollow SOPs to analyze samples from fermentation recovery and purification streamsPrepare samples from a variety of sample types using approaches such as dilution, extraction, and/or SPE clean upPrepare analytical standards, buffers and other reagents Conduct analysis of assay dataDocument findings in notebooks and reportsPresent results at internal meetings and write final reportAttend team meetingsQualificationsCurrently pursuing a degree in chemistry, biotechnology, or a related disciplineEnthusiastic and willing to learn new skillsStrong interest in biotechnology, renewable ingredients, and/or sustainabilityExcellent organizational skillsDetail orientedProficient with MS Office and MS ExcelExcellent written and oral communication skills Ability to work safely in a lab environmentBasic knowledge of statistics a plusProven analytical, problem solving, and customer relations skillsSelf-motivated, ability to multi-task, demonstrates flexibility in job assignmentExcellent written and verbal skillsEmbrace Amyris Core ValuesAdherence to Amyris Safety Policies and Procedures PI107827061

Integrated DNA TechnologiesID 2018-4485Job Locations US-IA-CoralvilleCategory Manufacturing Operations# of Openings 1Posted Date 16 hours agoShift/Schedule SuMTWTh 11P-8A (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:Follows custom instructions outlined by Oligo Master Records or Manager Approved Process FlowsKeeps thorough records of specialized processes in the oligo process historyOrganizes and handles customer owned materials as well as non-standard reagent formulationsHandles expensive oligos and reagentsPrepares standard and custom shipping paperwork and labels

ChobaniChobani is an equal opportunity employer. Chobani will not discriminate against any applicant for employment on any basis including, but not limited to: race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, marital status, predisposing genetic characteristics and genetic information, or any other classification protected by federal, state and local laws.Location: Twin Falls, IdahoCategory: Research & DevelopmentAs a Research and Development Pilot Plant Scientist, you will be responsible for leading and supporting the R&D Teams in scheduling trials and projects to be completed in the Pilot Plant. Additionally, the candidate will perform the prior set-up, the monitoring and analyzing of the equipment during the trails. Work activities will also include following/preparing protocols, SOPs and final study reports, as well as general lab operations. The ability to independently organize, design, carryout and analyze data and report the results of their work in a concise and well documented manner are important aspects of the position. The responsibilities of this position include:Lead in the planning and execution of pilot trials to develop new products under the direction of the R&D ScientistsLead and assist industrial trials through to commercialization of new products as well as recommendations on dry ingredient management in the Twin Falls plantTrain pilot plant personnel, R&D Scientists as well as Chobani Operations and Quality team on new R&D standards and documentationSet up, operate and perform routine maintenance/PM of pilot plant equipment, including but not limited to all process equipment and lab testing devices and instrumentsKeep accurate records of trial data as well as laboratory work. Collect, prepare and analyze data in conjunction with R&D Manager/DirectorAssist in day to day operations, including production of bench top and sales samples, physical, chemical, and sensory evaluation of food ingredients and finished productsManagement of shipments of ingredients to vendors within US and overseas as well as finished good sales sample dispatch in coordination with regional sales managersAssist with clean-up and maintenance in the laboratory and pilot plant as well as ingredient and finished good storage facilitiesOrder ingredients and lab supplies internally and through external vendorsLog all incoming ingredients by projects, arrange for adequate storage and develop tracking and inventory system to keep inventory of samples and ingredients in the R&D labApply all company quality standards while performing inspections, audits, and commissioning of high-tech Greek yogurt processing equipment, must also comply with all federal, state, local and company regulations including, ISDA, OSHA, FDA, EPA and SQFLead cost saving/optimization initiatives as well as overall R&D program improvements and utilize Root Cause Analysis when necessaryPrepare for all quality inspections and commissioning work by reviewing construction plans, specifications, installation manuals, etc. Complete site-specific quality/testing/commissioning plans based on requirements and Chobani standardsFollow Chobani safety and GMP procedures and practicesThe requirements of this position include:Minimum B.S. Food Science or related degree. Advanced degree strongly preferred3-5 years of food industry experience required, dairy knowledge is a plusPrior experience in food industry manufacturing and pilot plant/lab set up highly preferred.Familiarity with Lean product development, basic research tools and statistical analysisHighly versatile & technically talented individual who can work on highly complex equipment and processesMaintain clean & safe manufacturing environment within all facilitiesExcellent verbal and written communication skills, good MS Office skillsAbility to work independently and in group settingsExperience in operating or maintaining manufacturing equipment in a food / beverage environment preferredOccasional travel may be necessaryWorking knowledge of Good Laboratory Practices and current Good Manufacturing PracticesAbout Us:Since our founding 10 years ago, we've always been a different kind of company. After moving to New York from his native Turkey, our CEO Hamdi Ulukaya found that in America, yogurt just wasn't as delicious or widely available as it was back home. He thought everyone deserved better options, so he set about making delicious, nutritious, natural, and accessible Greek Yogurt right here in the U.S.Our mission since day one has been to provide better food to more people. And now as the No. 1-selling Greek Yogurt brand in America and the second largest overall yogurt manufacturer, we believe every food maker has a responsibility to provide people with better options, which is why we're so proud of the way our food is made.Our food philosophy of crafting quality products with simple ingredients is what makes Chobani a different kind of yogurt. Our belief that business done right has the ability to change lives and strengthen communities is what makes Chobani a different kind of company. From the way we source our ingredients to how we treat our employees, Chobani strives to make universal wellness happen sooner with everything we do. Certified as a Great Place to Work ® for the last two years, our culture is built on shared passion, dedication, and a commitment to doing what is right. Together, the Chobani family has created something unlike what any company has done before. The possibilities are endless.PI107808307

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

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

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