Associate Director, Epidemiology Analytics Daiichi Sankyo, Inc.Associate Director, Epidemiology AnalyticsBasking Ridge, NJ$157,920–$236,880 / yearFull timeProvide data management of diverse data (e.g., real-world setting and clinical trial) to set up epidemiologic data sets for various approaches, quantitative epidemiologic data analysis, interpretation of results, visualization of results, and generate manuscripts to disseminate findings. Doctorate Degree (PhD) in Biostatistics, Data Science, Statistics, Applied Mathematics, Epidemiology or related field plus a minimum of 4 years of experience in epidemiologic methods and data analysis (pharmaceutical industry in safety or associated service provider experience is preferred).
Associate Scientist, QC Operation WuXi Biologics Cayman IncAssociate Scientist, QC OperationCranbury, NJ$49,700–$79,500 / yearSupport stability study program as backup stability coordinator, including but not limited to stability study protocol review, stability study initiation, stability sample management, and stability summary report generation. Job Respsonsibilities: In charge of QC sample management, including but not limited to sample receiving, aliquoting, and distribution for testing by using either LIMS lot disposition module or paper-based forms if LIMS is unavailable.
Associate Scientist The ChemoursAssociate ScientistNewark, New JerseyIn key sectors such as clean energy, advanced electronics, high-performance computing and AI, climate friendly cooling, and high-quality paints and coatings for homes and industrial infrastructure---sustainable solutions and more modern living depend on Chemours chemistry. Pay Range (in local currency): $73,947.00 - $115,542.00 Chemours Level: 23 Annual Bonus Target: 6% The pay range and incentives listed above is a general guideline based on the primary location of this job only and not a guarantee of total compensation.
Associate Research Scientist ETSAssociate Research ScientistPrinceton, NJProvide scientific and technical skills so as to contribute to conceptualizing, designing, obtaining support for, conducting, and managing one or more of the following: (1) research projects or (2) development projects, particularly those for which scientific principles are applied to the creation of tools to improve the efficiency or quality of the practice of test development or statistical analysis; new item types; (3) the scoring of responses to open-ended items; (4) innovative assessment prototypes or products. Participate in dissemination activities through the publications of research papers in peer review journals and in the ETS Research Report series, the issuing of progress and technical reports, the presentation of seminars at major conferences and at ETS, or the use of other appropriate communication vehicles, including books and chapters, that impact practice in the field or at ETS.
HTP Production Associate Scientist - Automation Workflows GenScript/ProBioHTP Production Associate Scientist - Automation WorkflowsPiscataway, NJ$60,000–$75,000 / yearGuided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions. The ideal candidate is comfortable working with automated laboratory systems, possesses strong organizational skills, and has experience with laboratory data management platforms such as ELN, LIMS, or similar systems.
HTP Analytical QC Associate Scientist GenScript/ProBioHTP Analytical QC Associate ScientistPiscataway, NJ$60,000–$75,000 / yearGuided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions. Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products.
HTP Analytical QC Associate Scientist GenScript ProBioHTP Analytical QC Associate ScientistPiscataway, New JerseyGuided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions. Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products.
Associate Scientist, MSAT Cell & Gene Therapy Legend Biotech CorpAssociate Scientist, MSAT Cell & Gene TherapySomerset, NJ$83,711–$104,637 / yearHeadquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. This role combines cell therapy manufacturing studies with basic lab operations, supporting automated instrument workflow studies and managing inventory and availability of materials in a fast-paced, GMP-regulated environment.
Associate Principal Scientist, DSCS Digital Technologies-Laboratory Automation, Semantic Technologies & Scientific Data Integration Merck & Co IncAssociate Principal Scientist, DSCS Digital Technologies-Laboratory Automation, Semantic Technologies & Scientific Data IntegrationRahway, NJ$142,400–$224,100 / yearRequired Skills: Animal Vaccination, Animal Vaccination, Biopharmaceutical Industry, Cell Line Development, Computer Science, Data Integration, Data Science, Detail-Oriented, Downstream Process Development, Drug Delivery Technology, Drug Development, Expression Vectors, Informatics, Interpersonal Relationships, Laboratory Automation, Leading Project Teams, Materials Science, Molecular Biology, Oncology, Pharmaceutical Development, Pharmaceutical Formulations, Pharmaceutical Process Development, Pharmaceutical Sciences, Physical Characterization, Scientific Data Management {+ 1 more}. Working at the intersection of pharmaceutical science, digital technologies, and data integration, the candidate will support the development of semantic models, ontologies, and knowledge graph frameworks that improve interoperability, traceability, discoverability, and consistency across scientific systems.
HTP Analytical QC Associate Scientist Genscript Biotech CorpHTP Analytical QC Associate ScientistPiscataway, NJ$60,000–$75,000 / yearGuided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions. Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products.
HTP Production Associate Scientist Genscript Biotech CorpHTP Production Associate ScientistPiscataway, NJ$60,000–$75,000 / yearGuided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions. The ideal candidate is comfortable working with automated laboratory systems, possesses strong organizational skills, and has experience with laboratory data management platforms such as ELN, LIMS, or similar systems.
Associate Research Scientist Educational Testing ServiceAssociate Research ScientistPrinceton, NJProvide scientific and technical skills so as to contribute to conceptualizing, designing, obtaining support for, conducting, and managing one or more of the following: (1) research projects or (2) development projects, particularly those for which scientific principles are applied to the creation of tools to improve the efficiency or quality of the practice of test development or statistical analysis; new item types; (3) the scoring of responses to open-ended items; (4) innovative assessment prototypes or products. Participate in dissemination activities through the publications of research papers in peer review journals and in the ETS Research Report series, the issuing of progress and technical reports, the presentation of seminars at major conferences and at ETS, or the use of other appropriate communication vehicles, including books and chapters, that impact practice in the field or at ETS.
Associate Research Scientist RD PartnersAssociate Research ScientistLawrenceville, New Jersey£65,977–£82,472Experimental techniques could include, but are not limited to, the following: Processing human tissue and blood, Cell-based assays, Flow cytometry, ELISAs/MSD assays, RNA extraction and cDNA synthesis, Gene expression array cards. The qualified candidate will process human samples, maintain the laboratory's biobank (including sample storage and retrieval), and perform a range of experimental procedures under the guidance of senior scientists.
Associate Principal Scientist, Analytical R&D Merck & Co IncAssociate Principal Scientist, Analytical R&DRahway, NJ$142,400–$224,100 / yearJoin us and experience our culture firsthand - one of strong ethics & integrity, diversified experiences, exceptional science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. Your main responsibilities will include: Driving Pipeline: Leading or participating on analytical teams driving the development of drugs in the company's pipeline, with a deep understanding of product development from early stage through commercialization.
NewAssociate Principal Scientist Engineer, Drug and Device Combination Products (Onsite) Merck & Co IncAssociate Principal Scientist Engineer, Drug and Device Combination Products (Onsite)Rahway, NJ$142,400–$224,100 / yearRequired Skills: Analytical Chemistry, Chemical Biology, Collaborative Development, Combination Products, Design Failure Mode and Effect Analysis (DFMEA), GMP Compliance, Mechanical Engineering, Mechanical Testing, Medical Device Quality Systems, Medicinal Chemistry, Project Management, Project Management Support, Quality Control Management, Quality Management Systems (QMS), Test Method Validation. The Associate Principal Scientist / Engineer of Method Development, Testing & Transfer will be responsible for helping to lead the Center of Excellence (CoE) focused on developing and validating platform and innovative device/CP functional test methods with high technical rigor in support of development activities, IND-enabling stability, commercial stability, and Design Verification.
Associate Scientist WuXi Biologics Cayman IncAssociate ScientistCranbury, NJAssociate Scientist supports Quality Control laboratory operations through preparation of reagents and buffers, glassware management, laboratory organization, and general support of physicochemical testing activities. Associate's degree in Chemistry, Biochemistry, Biology, or a related scientific field preferred; equivalent laboratory experience may be considered.
NewAssociate Principal Scientist - ADME Just-Evotec BiologicsAssociate Principal Scientist - ADMEPrinceton, New JerseyAbility to perform high-impact as well as high throughput studies to completion in a fast paced environment, while managing multiple projects to meet the timelines. Provides scientific knowledge and responsible in establishing new TOX assays as well as contribute to the continuous improvement of the current TOX assays.
Associate Principal Scientist - In Vitro Toxicology - Microelectrode Array - Site Based, Princeton, NJ Just-Evotec BiologicsAssociate Principal Scientist - In Vitro Toxicology - Microelectrode Array - Site Based, Princeton, NJPrinceton, New JerseyAbility to perform high-impact as well as high throughput studies to completion in a fast paced environment, while managing multiple projects to meet the timelines. Provides scientific knowledge and responsible in establishing new TOX assays as well as contribute to the continuous improvement of the current TOX assays.
Associate Scientist, Protein Characterization Insmed IncAssociate Scientist, Protein CharacterizationNJ$103,000–$131,000 / yearFor New York City Residents: To assist in identifying candidates with qualifications matching those required and/or preferred for this role, Insmed uses an Automated Employment Decision Tool ("AEDT") that employs artificial intelligence to analyze and score information provided in resumes and application materials including, but not limited to, skills, work experience, education, and job-related qualifications. Desire to expand knowledge in advanced analytical and biophysical techniques to characterize proteins including light scattering (e.g., DLS, SEC-MALS, batch MALS), circular dichroism, fluorescence, Amide IFTIR, thermal stability (DSC), and sub-visible particle analysis.
Associate Principal Scientist, Statistical Programming Merck & Co IncAssociate Principal Scientist, Statistical ProgrammingRahway, NJ$144,373–$224,100 / yearPosition Requirements: Must possess significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; and programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic data (raw concentration data, derived PK parameters). Education Requirements: Must have a Bachelor's degree (or US equivalent) in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering, Pharmaceutical Sciences, or related field plus 9 years SAS programming experience in a clinical trial environment.
Associate Principal Scientist, Microbiology Testing, EM/Utilities Monitoring Program - Onsite/First Shift Merck & Co IncAssociate Principal Scientist, Microbiology Testing, EM/Utilities Monitoring Program - Onsite/First ShiftRahway, NJ$142,400–$224,100 / yearRequired Skills: Analytical Method Development, Assay Development, Biological Assay Development, Biological Sciences, Cell-Based Assays, Chromatographic Techniques, Contamination Control, Cross-Functional Teamwork, Good Manufacturing Practices (GMP), High Resolution Mass Spectrometry (HRMS), Laboratory Information Management System (LIMS), Liquid Chromatography-Mass Spectrometry (LC-MS), Mass Spectrometry Analysis, Microbiological Test, Microbiology, Process Analytical Technology (PAT), Protein Analysis. Leverage QC microbiology expertise as a subject matter expert in support of sterile operations within the quality control department including isolator qualifications, sterility testing, biological indicator challenge tests, and method suitability, endotoxin, microbial enumeration, media / reagent quality control testing, mycoplasma.
Applied AIML Data Scientist-Senior Associate JPMorgan Chase Bank, N.A.Applied AIML Data Scientist-Senior AssociateJersey City, NJFull timeThe Legal Applied AI/ML team in Corporate Technology at JPMorgan Chase focuses on solving challenging business problems such as semantic search, question answering, document analysis, automation of service inquiries through data science and ML techniques, particularly using GenAI and LLM tools and techniques. As an Applied AI ML Data Scientist-Senior Associate on Corporate team, you will have the opportunity to study complex business problems and apply advanced algorithms to develop, test, and evaluate AI/ML applications or models for those problems.
Associate Director, Patient Safety Scientist Bristol-Myers Squibb CoAssociate Director, Patient Safety ScientistMadison, NJ$150,300–$182,125 / yearResponsible for creation and update of the EDSR to proactively characterize emerging safety concerns during asset development, support Structured Benefit Risk, and define the strategy for Company Core Risk Management and gaining alignment with SMT/governance, including collaboration with Epidemiology on risk minimization effectiveness, non-interventional research (NIR) activities for post-authorization safety studies (PASS). The Associate Director, Patient Safety Scientist, is a key partner and strategic advisor to Medical Safety Assessment Physician (MSAP)/Safety Management Team (SMT) Chair to characterize conditions for safe use of BMS medicines and proactively communicate safety evidence to influence decision-making for assets in development and marketed products by evaluating and mitigating risks.
Associate Principal Scientist, Stat. Programming - A&R Standards, Innovation (Hybrid) Merck & Co IncAssociate Principal Scientist, Stat. Programming - A&R Standards, Innovation (Hybrid)Rahway, NJ$142,400–$224,100 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Ability to comprehend analysis plans which may describe methodology to be programmed; understanding of statistical terminology and concepts; Implements statistical methods not currently available through commercial software packages.
Associate Principal Scientist Evotec SEAssociate Principal ScientistPrinceton, NJ$93,500–$115,000 / yearAbility to perform high-impact as well as high throughput studies to completion in a fast paced environment, while managing multiple projects to meet the timelines. Provides scientific knowledge and responsible in establishing new TOX assays as well as contribute to the continuous improvement of the current TOX assays.
Associate Principal Scientist - In Vitro Toxicology - Microelectrode Array - Site Based, Princeton, NJ Evotec SEAssociate Principal Scientist - In Vitro Toxicology - Microelectrode Array - Site Based, Princeton, NJPrinceton, NJ$93,500–$126,500 / yearAbility to perform high-impact as well as high throughput studies to completion in a fast paced environment, while managing multiple projects to meet the timelines. Provides scientific knowledge and responsible in establishing new TOX assays as well as contribute to the continuous improvement of the current TOX assays.
Associate Scientist Trilon GroupAssociate ScientistEast Brunswick, NJ$60,000–$70,000 / yearWith expertise spanning civil/site engineering, environmental permitting, transportation infrastructure, construction management, and advanced surveying technologies, we are committed to delivering high-quality, timely solutions to local, state, and federal clients. Artheon is a trusted engineering and consulting firm offering services that rival large organizations while maintaining the personalized client relationships of a boutique firm.
Associate Scientist IMCD NVAssociate ScientistAllendale, NJ$75,000–$95,000 / yearMinimum 6 years of related experience in formulation development with a focus on solid oral dosage forms; hands-on experience with powder handling, blending, wet granulation, milling, tablet compression, capsule filling, film coating, or fluid bed processing; experience performing USP testing, including dissolution, disintegration, friability, and tablet hardness. Working closely with the Senior Scientist, this role will support customer projects, supplier collaborations, technical demonstrations, and internal application studies involving oral solid, liquid, and topical dosage forms while following GLP, safety, quality, and regulatory requirements.
Associate Director, Global Drug Safety & Pharmacovigilance Scientist Genmab ASAssociate Director, Global Drug Safety & Pharmacovigilance ScientistPrinceton, NJFor 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. Contribute to safety-related documents for Genmab products throughout product lifecycle from FIH to post-marketing, including robust safety surveillance, Safety Assessment Reports for potential signals/risks, RSI in IB, ADR in the CCDS and product labels, Aggregate Safety Reports (e.g.
Associate Principal Scientist, Post Market Safety, L''Oréal Research & Innovation L'Oreal USA IncAssociate Principal Scientist, Post Market Safety, L''Oréal Research & InnovationNJResearch & Innovation. 13-Apr-2026.
NewAssociate Principal Scientist - ADME CyprotexAssociate Principal Scientist - ADMEPrinceton, New JerseyAbility to perform high-impact as well as high throughput studies to completion in a fast paced environment, while managing multiple projects to meet the timelines. Provides scientific knowledge and responsible in establishing new TOX assays as well as contribute to the continuous improvement of the current TOX assays.
Associate Principal Scientist - In Vitro Toxicology - Microelectrode Array - Site Based, Princeton, NJ CyprotexAssociate Principal Scientist - In Vitro Toxicology - Microelectrode Array - Site Based, Princeton, NJPrinceton, New JerseyAbility to perform high-impact as well as high throughput studies to completion in a fast paced environment, while managing multiple projects to meet the timelines. Provides scientific knowledge and responsible in establishing new TOX assays as well as contribute to the continuous improvement of the current TOX assays.
Associate Scientist ArtheonAssociate ScientistEast Brunswick, New Jersey$60,000–$70,000 / yearWith expertise spanning civil/site engineering, environmental permitting, transportation infrastructure, construction management, and advanced surveying technologies, we are committed to delivering high-quality, timely solutions to local, state, and federal clients. About Artheon Artheon is a trusted engineering and consulting firm offering services that rival large organizations while maintaining the personalized client relationships of a boutique firm.
Associate Scientist Peptide Formulation - Contract Protagonist TherapeuticsAssociate Scientist Peptide Formulation - ContractNewark, New JerseyExperience And Skills 8+ years of experience in peptide or small molecule development with BS in chemistry, engineering, pharmaceutics, or other related scientific discipline (or) 5-8 years with MS in chemistry, engineering, pharmaceutics, or other related scientific discipline (or) 3-5 years of experience in drug formulation with PhD in chemistry, engineering, pharmaceutics, or other related scientific discipline. The Company also has a number of preclinical stage drug discovery programs addressing clinically and commercially validated targets including an oral IL-17 peptide antagonist, obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin programs.
FSP Associate Research Scientist: Analytical Outsourcing Thermo Fisher Scientific IncFSP Associate Research Scientist: Analytical OutsourcingNew Brunswick, NJ$90,000–$110,000 / yearSummary: The Analytical Outsourcing manages end-to-end testing programs, research specifications, and quality oversight for raw materials and packaging components supporting clinical drug product manufacturing, within the External Partner Management team, part of Product Development Operations. Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.
Associate Scientist Bristol-Myers Squibb CoAssociate ScientistSummit West, NJ$71,910–$87,138 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. This includes execution of thorough root cause investigations, interviewing personnel, hypothesis testing and interpretation of results, authoring investigation reports, identifying corrective and preventive actions (CAPA), and troubleshooting complex problems.
Associate Scientist I Ewing A-TEKAssociate Scientist I EwingEwing, New JerseyWe may assess application materials for job-related technical depth, internal consistency, and demonstrated hands-on experience, including through follow-up questions, skills assessments, or reference checks. Candidates may use tools (including AI) for proofreading or formatting; however, using any tool to fabricate, exaggerate, or misrepresent qualifications, experience, or work product is not permitted.
Associate Environmental Scientist Sundance Consultants LLCAssociate Environmental ScientistFlorham Park, NJField work will include oversight of subcontractors, including drillers and other laborers, during soil boring advancement, monitoring well installation, excavation activities, and remedial construction activities; and sampling various media including soil, groundwater, sediment, soil vapor and air. Its diverse expertise encompasses environmental remediation, urban planning, engineering iconic coastal and marine structures, developing sustainable energy sources, and pioneering resource extraction methods.
Associate Principal Scientist, Combination Product Design Verification (Associate Director Equivalent) Merck & Co IncAssociate Principal Scientist, Combination Product Design Verification (Associate Director Equivalent)Rahway, NJ$142,400–$224,100 / yearRequired Skills: Collaborative Development, Combination Products, Commercialization, Design Controls, Design Failure Mode and Effect Analysis (DFMEA), Design Verification Testing, Device Development, Human Factor Engineering, Manufacturing Processes, Mechanical Engineering, Mechanical Testing, Medical Device Quality Systems, Method Validation, Product Risk Management, Project Leadership, Quality Management Systems (QMS), Release Testing, Self Motivation, Testing Methodology, Test Method Validation, Test Procedure Development, Troubleshooting. This role has a primary focus on design verification while encompassing the full spectrum of testing activities, including test method development and validation, analytical transfers, incoming testing, in-process, release testing, and testing readiness to enable successful clinical introduction and commercialization.
Order Management Associate Scientist GenScript/ProBioOrder Management Associate ScientistPiscataway, NJ$60,000–$75,000 / yearGuided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions. The position works closely with Production, Project Management, and cross-functional teams to coordinate planning, track progress, and support efficient end-to-end project delivery in a collaborative and fast-paced environment.
Order Management Associate Scientist GenScript ProBioOrder Management Associate ScientistPiscataway, New JerseyGuided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions. The position works closely with Production, Project Management, and cross-functional teams to coordinate planning, track progress, and support efficient end-to-end project delivery in a collaborative and fast-paced environment.
Associate Principal Scientist, Human Factors Merck & Co IncAssociate Principal Scientist, Human FactorsRahway, NJ$142,400–$224,100 / yearRequired Skills: Combination Products, Commercialization, Design Controls, Human Factor Engineering, Human Factors, Labels, Medical Devices, Regulatory Requirements, Risk Assessments, Risk Management, Test Method Validation, Troubleshooting, Usability Testing, User Research. Key Responsibilities and Activities: Lead Human Factors Project Work (Execution and Strategy), including, but not limited to: Establish and own HF strategy from early concept through validation and post-market for devices and combination products.
Associate Principal Scientist, Engineering Merck & Co IncAssociate Principal Scientist, EngineeringRahway, NJ$142,400–$224,100 / yearRequired Experience and Skills: For BS/MS candidates, at least 8 years of relevant work experience post-graduation - OR - for PhD candidates with at least 3 years of relevant work experience post PhD defense, where relevant work experience would include the following: Experience performing lab-based research/process development in a chemical engineering-related area. Under scientific and administrative direction, an engineer in this role conducts independent research which involves conceiving, designing, planning, and implementing advanced experiments aimed at achieving research goals related to process development, technology development, and production of active pharmaceutical ingredients (API).
Associate Scientist, Microbiology Genscript Biotech CorpAssociate Scientist, MicrobiologyPennington, NJ$55,000–$70,000 / yearProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017. About the Position: The position reports to the Microbiology Manager, is ideally suited for a professional with extensive technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer.
NewAssociate Environmental Scientist True EnvironmentalAssociate Environmental ScientistFlorham Park, New JerseyField work will include oversight of subcontractors, including drillers and other laborers, during soil boring advancement, monitoring well installation, excavation activities, and remedial construction activities; and sampling various media including soil, groundwater, sediment, soil vapor and air. Its diverse expertise encompasses environmental remediation, urban planning, engineering iconic coastal and marine structures, developing sustainable energy sources, and pioneering resource extraction methods.
Order Management Associate Scientist Genscript Biotech CorpOrder Management Associate ScientistPiscataway, NJ$60,000–$75,000 / yearGuided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions. The position works closely with Production, Project Management, and cross-functional teams to coordinate planning, track progress, and support efficient end-to-end project delivery in a collaborative and fast-paced environment.
Associate Scientist - Downstream Avantor IncAssociate Scientist - DownstreamBridgewater, NJ$69,000–$110,975 / year3rd Party Non-Solicitation Policy: By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. How you will thrive and create and impact: Downstream Process Execution: Perform bench-scale purification of biologics, such as monoclonal antibodies, bispecific, fusion proteins, or AAV, independently or in collaboration with other scientists.
Associate Director, Global Clinical Scientist (Cell Therapy) Bristol-Myers Squibb CoAssociate Director, Global Clinical Scientist (Cell Therapy)Madison, NJ$211,910–$256,789 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Associate Scientist, Microbiology GenScript/ProBioAssociate Scientist, MicrobiologyPrinceton, NJ$55,000–$70,000 / yearProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017. The position reports to the Microbiology Manager, is ideally suited for a professional with extensive technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer.
Associate Scientist, Microbiology GenScript ProBioAssociate Scientist, MicrobiologyNew JerseyProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017. The position reports to the Microbiology Manager, is ideally suited for a professional with extensive technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer.