May 13, 2026For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at LeidosCareersFraud@leidos.com.
ul>Perform analytical testing for incoming, in-process and final products, and stability samples using equipment such as balances, pipettes, pH meter, UV/Visible spectrophotometer, Total Organic Carbon analyzer, etc. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis.
div>My client is expanding and seeks a Senior Scientist to investigate neurotransmitters, novel compounds, and large molecules in the CNS space.
Collaborate with management to help write study plans and reports and be able to discuss the data collection and analyses processes in a clear manner.
Princeton, New Jersey30+ days ago
This is a hands‑on, lab‑based role at our Princeton, NJ office—ideal for someone eager to deepen their expertise in ligand binding assays (LBAs) while supporting impactful bioanalytical work that fuels clinical trials worldwide. In this role, you will support our Ligand Binding team through a wide range of scientific and operational activities, including: Performing ligand binding assays (e.g., ELISA, ECL, RIA, cell‑based assays) in accordance with established methods, SOPs, and regulatory requirements.
Newark, New Jersey23 days ago
In 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. The 350 scientists, engineers, and technicians at the site work in 130 laboratories that provide 320,000 square feet of space for research and development, technical service, and manufacturing support of Chemours businesses.
Princeton, NJ30+ days ago
Ligand Binding Analytical Scientist II - Princeton, NJ in Princeton, NJ - Syneos Health Apply Inside Syneos Health Our Values Who We Are Our Solutions Diversity, Equity, And Inclusion Why Work Here Discover what our more than 29,000 employees already know: work here matters everywhere. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients.
Princeton, NJ30+ days ago
Clinical Research - Ligand Binding Analytical Scientist I in Princeton, NJ - Syneos Health Apply Inside Syneos Health Our Values Who We Are Our Solutions Diversity, Equity, And Inclusion Why Work Here Discover what our more than 29,000 employees already know: work here matters everywhere. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients.
Elizabeth, New Jersey30 days ago
PhD in Analytical Chemistry, Flavor/Fragrance Chemistry, Atmospheric Chemistry, Cosmetic Chemistry, or a related field with 5+ years of post-degree experience, or equivalent combination of advanced degree and demonstrated technical leadership. Excellent cross-functional communication skills, with a track record of translating complex analytical requirements into actionable plans for non-chemistry stakeholders (e.g., ML engineers, product teams).
Education Minimum Requirements: Minimum 3 years relevant industry experience for applicants with a Bachelor of Science degree, or 0 years of relevant industry experience for applicants with a Master of Science degree in Chemistry, Pharmaceutical Sciences, or related fields. In your role as Scientist, you will be part of a team of Analytical Chemists working on cross-functional scientific teams to enable novel small molecule, peptide, and oligonucleotide drug development through laboratory-based analytical characterization and statistical data analysis.
In this role, you will lead a small team of analytical chemists and play a key role in multidisciplinary innovation programs, delivering critical analytical insights that enable the development of impactful fragrance, taste, health, and nutrition solutions. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere.
The successful candidate will join a group of innovative analytical scientists with broad deliverables to support commercial pharmaceutical products, ensuring an undisrupted supply of our company products to patients globally. Bachelor's Degree (BS) in Chemistry or related discipline with at least seven (7) years of relevant pharmaceutical development experience, OR Master's Degree (MS) in Chemistry or related discipline with at least five (5) years of relevant pharmaceutical development experience, OR PhD in Analytical Chemistry or related discipline.
Branchburg, NJ30+ days ago
This role emphasizes hands-on laboratory work, technical leadership, and collaboration within a cross-functional team, with a strong focus on HPLC- and UPLC-based techniques for protein and antibody characterization. The Lead Analytical Scientist Chromatography will serve as a technical subject matter expert supporting chromatographic method development, optimization, and routine testing at a client site.
PhD in Analytical Chemistry, Flavor/Fragrance Chemistry, Atmospheric Chemistry, Cosmetic Chemistry, or a related field with 5+ years of post-degree experience, or equivalent combination of advanced degree and demonstrated technical leadership. Mentor and technically develop junior and mid-level scientists, establishing best practices, reviewing work for scientific integrity, and elevating the teams overall analytical capability.
Join 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.
ProBio 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. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
ProBio 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. Guided 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 Senior Scientist - Analytical Development plays a key role in our company' animal health research and development, by supporting the analytical development of high priority drug candidates and execute studies to characterize key physical and chemical properties of active pharmaceutical ingredients, excipients, and formulated drug products (e.g., tablets, solutions, implants). Techniques often used by persons in these positions include separation techniques (e.g., HPLC, GC, TLC), in-vitro dissolution, general/wet chemical methods, physical characterizations (e.g., particle size analysis, SEM and light microscopy), spectroscopy (e.g., UV/Vis and FTIR) and thermal methods (e.g., DSC, TGA).
The Associate Principal Scientist is a laboratory-based scientific role tasked with solving complex analytical problems at the interface of biology, chemistry, and lab informatics disciplines to enable development of Biologics drug substances and drug products. A strong team player with excellent oral and written communication skills; ability to work both independently for development of assays and cross-functionally for successful transfer of assays.
The Senior Scientist is a laboratory-based scientific role tasked with solving complex analytical problems at the interface of biology, chemistry, and lab informatics disciplines to enable development of Biologics drug substances and drug products. A strong team player with excellent oral and written communication skills; ability to work both independently for development of assays and cross-functionally for successful transfer of assays.
Must possess in-depth knowledge of analytical chemistry techniques, such as spectrophotometric, dissolution and drug release, chromatographic techniques and measuring physical parameters (viscosity, particle size or droplet size by laser diffraction, melting point by DSC, water content by TGA, identification by XRPD, and other techniques). The individual is a part of the Quality Control Technical Services team which develops, validates/verify, and qualifies testing methods for active pharmaceutical ingredients, excipients and dosage forms, including troubleshooting and lifecycle management of analytical methods.
This position offers the opportunity to make a meaningful impact by advancing real-time analytical capabilities, enabling process monitoring and control, as well as supporting technology transfer and launch readiness efforts for programs progressing from early development into manufacturing. B.S. in chemistry, biochemistry, biotechnology, bioengineering, chemical engineering, or a related discipline with a minimum of 6 years of relevant industry experience; or.
p>In your role as Senior Scientist, you will be part of a team developing innovative analytical methodologies for early to late phase programs with application to drug substance and a broad array of drug product dosage forms, combination products and modalities through analytical characterization, imaging tools, and data analysis. Your main responsibilities include:
For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. Qualifications - B.S. or M.S. in Chemistry, Chemical Engineering, Biochemistry, Biology or similar life sciences and relevant years of experience in analytical chemistry or biologics testing laboratory: Scientist 3 - B.S. with 3 to 5 years of experience; M.S. with 1 to 2 years of experience.
In your role as Scientist, you will be a critical part of the Analytical Research and Development Microbiology team with responsibilities including leading the rapidly growing pipeline via collaboration with stakeholders to deliver on critical data in a good manufacturing practices (GMP) microbiology laboratory, including finished products testing, utilities, and environmental monitoring. Support of sterile operations within the quality control department including utilizing isolator for sterility testing, conduct method suitability testing, endotoxin, microbial enumeration, media / reagent quality control testing.
p>Description: The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Creates and maintains laboratory record documentation (notebooks and computer-based), documents exact steps followed during analysis execution, calculates and reports results in a timely manner.
p>For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. Qualifications - B.S. or M.S. in Chemistry, Chemical Engineering, Biochemistry, Biology or similar life sciences and relevant years of experience in analytical chemistry or biologics testing laboratory:
- Scientist 3 - B.S. with 3 to 5 years of experience; M.S. with 1 to 2 years of experience.
For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. We are looking for a Scientist III or Principal Scientist I – Liquid Chromatography – Mass Spectrometry (LC-MS) and Analytical Support to work as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Rahway, NJ.
Pennington, NJ30+ days ago
ProBio 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. GenScript''s businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
Piscataway, NJ17 days ago
GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. This role is responsible for performing analytical characterization and quality control testing of recombinant proteins generated from high-throughput production workflows.
Piscataway, New Jersey14 days ago
Guided 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.
Qualifications: Bachelor's degree in Analytical Chemistry, Biochemistry, or related field with a minimum of 4 years of industry analytical development or quality control experience. Job Responsibilities: Conduct assay development, transfer, optimization, assessment, and routine testing for ELISA-based assays, PCR-based assays, and cell-based assays.
Piscataway, NJ30+ days ago
Established in 1806 as a small soap and candle business in New York City, Colgate-Palmolive is now a truly global company with products sold in over 200 countries and territories under such internationally recognized brand names as Colgate, Palmolive, Softsoap, Irish Spring, Protex, Sorriso, Kolynos, elmex, Tom's of Maine, Sanex, Ajax, Axion, Soupline, Haci Sakir, Suavitel, PCA SKIN, EltaMD, Filorga and Hello as well as Hill's Science Diet and Hill's Prescription Diet. Colgate-Palmolive is a leading consumer products company that serves hundreds of millions of consumers worldwide with brands and products across four core businesses - Oral Care, Personal Care, Home Care and Pet Nutrition.
Drives research strategy including independently managing analytical method development/validation (mostly LC and GC) for active pharmaceutical ingredients, excipients and dosage forms to be used in the analytical R&D laboratory for routine analysis. Interpret and communicate complex experimental results, present technical findings to internal R&D & management teams and document findings in internal technical reports and/or external publications.
Within the Global Quality Large Molecule Analytical Sciences (GQ- LMAS) organization, this Analytical Transfer Team includes activities interfacing with a global network of product manufacturing and testing sites, collaborating with product development groups within our our company Manufacturing Division and our our company's Research Laboratories division, continuous improvement of analytical methodology, assay validation, analytical technical transfer, and Biologics License Application preparation. Global Quality Large Molecule Analytical Sciences (GQ-LMAS), in our company's Manufacturing Division, is accountable for the commercialization of large molecule, vaccines and biologics, analytical techniques from Phase III through launch and transfer to supply.
Summit West, NJ13 days ago
Based 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.
New Jersey, NJ30+ days ago
For 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. Hands on experience and deep understanding of techniques like Peptide mapping, HPLC/UPLC (IEX, SE, RP), SEC-MALS, DLS, DSC, CD & CE-SDS along with impurity assays for HCP, residual Protein A, residual host cell DNA, Bioburden and Endotoxin detection.
Bridgewater, NJ27 days ago
Cellares is seeking an innovative and highly motivated Senior Analytical Transfer Scientist with expertise in method transfer, validation and development of bioanalytical methods to support the Cell therapy Analytical Science and Technology team. This individual will interface cross-functionally across the Quality control, Manufacturing Science and Technology, Quality, Analytical Development team, Regulatory and serve as the analytical subject matter expert (SME) in supporting product development and regulatory submission.
This role will focus on the establishment, development and qualification of flow cytometry-based methods, cell-based potency assays, and other bioanalytical strategies to support the release, characterization and stability assessment of cell therapy products (multiple types of cell product, in vivo vector product, etc). Headquartered 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.
Headquartered 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. The individual will be responsible for analytical methods development, qualification and internal or external transfer; routine testing of final product (GMP), stability, and in-process samples; and performing data review and verification, lab and instrument maintenance etc.
Pennington, NJ30+ days ago
ProBio 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. Scientist, Analytical Operations, 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.
Piscataway, NJ30+ days ago
GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. This role is responsible for performing analytical characterization and quality control testing of recombinant proteins generated from high-throughput production workflows.
Pennington, NJ17 days ago
ProBio 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. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
ProBio 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. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
Piscataway, NJ30+ days ago
The individual in this capacity performs analytical methods qualifications/validations, analyzes active pharmaceutical ingredients, excipients, and finished dosage forms using appropriate analytical methods and maintains/qualifies analytical equipment. Essential Functions: • Performs analysis and release of active pharmaceutical ingredients, excipients, in-process materials, and finished drug products to support the formulation development team, maintaining full compliance with all applicable US FDA - cGMP regulations and internal SOPs.
Pennington, NJ30+ days ago
GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. QC 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.
p>Required Skills: Analytical Chemistry, Analytical Development, Biochemistry, Capillary Electrophoresis (CE), Chromatography, ELISA Techniques, Gel Electrophoresis, High-Performance Liquid Chromatography (HPLC), Immunoassays, Laboratory Techniques, Oral Communications, Polymerase Chain Reaction (PCR), Size Exclusion Chromatography (SEC), Technical Writing, Ultra Performance Liquid Chromatography (UPLC). The Scientist is a laboratory-based scientific role tasked with solving complex analytical problems at the interface of biology, chemistry, and lab informatics disciplines to enable development of Biologics drug substances and drug products.
Bridgewater, NJ8 days ago
Analytical Chemist / QC Scientist I performs fit-for-purpose testing in support of manufacturing, including in-line and finished product release testing using various analytical techniques. ResponsibilitiesPerform fit-for-purpose testing following operating procedures in support of manufacturing, including in-line and finished product release testing using various analytical techniques.
Bridgewater, NJ30+ days ago
p>Henkel holds leading positions in both industrial and consumer businesses: Our portfolio includes well-known hair care products, laundry detergents, fabric softeners as well as adhesives, sealants, and functional coatings. This position is with our Adhesive Technologies business unit - where we empower our people to transform industries and provide our customers with a competitive advantage through adhesives, sealants and functional coatings.