Senior Scientist, Analytical R&D

Senior Scientist – Pharmaceutical Analytical Sciences

The Pharmaceutical Analytical Sciences group has an opening for a Senior Scientist based in Rahway, NJ. Join us and experience our culture first‑hand – one of strong ethics & integrity, diversified experiences, exceptional science and a passion for improving human health through innovative drug delivery technologies and predictive analytical tools.

• Drive solutions to analytical development challenges for synthetic small molecules, peptides and oligonucleotide active pharmaceutical ingredients and pharmaceutical products using conventional and novel technologies.
• Design scientific studies to inform the selection and deep understanding of synthetic routes, formulation compositions, and manufacturing processes.
• Implement analytical methods for laboratory development, release and shelf‑life assessment of clinical supplies under GMP conditions.
• Provide leadership on drug development pipeline projects and on innovative technology teams shaping analytical methods and tools of the future.
• Author regulatory submission documents across the project life‑cycle and respond to agency questions.
• Document work in a detailed and timely manner.
• Collaborate effectively with internal and external partners.
• Present results of experiments and innovation efforts to project teams and at cross‑functional forums.
• Engage in the external scientific community through participation in professional organizations, conferences and publications.

5‑10% travel.

• PhD in Chemistry, Pharmaceutical Science, or related discipline.
• Master’s degree in chemistry, Pharmaceutical Sciences, or related discipline plus at least 3 years of pharmaceutical industry experience.
• Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or related discipline plus at least 7 years of industry experience.

• Proven record of strong technical problem solving and innovative research supported by scientific publications.
• Excellent written and oral communication skills.
• Strong leadership, collaboration and interpersonal skills.

• Experience with large molecule characterization (oligonucleotides, enzymes, peptides, etc.).
• Chromatography (LC, GC) method development, analysis and troubleshooting.
• Other advanced analytical techniques such as mass spectrometry or dissolution.
• Data science.

• Adaptability
• Analytical Method Development
• Assay Development
• Bioanalytical Analysis
• Biochemical Assays
• Biopharmaceuticals
• Cell‑Based Assays
• Chromatographic Techniques
• Chromatography
• Clinical Trials
• Data Science
• Dosage Forms
• GMP Compliance
• GMP Environments
• Innovative Thinking
• Medicinal Chemistry
• Nuclear Magnetic Resonance (NMR) Analysis
• Pharmaceutical Sciences
• Process Analytical Technology (PAT)
• Project Management
• Regulatory Submissions
• Ribonucleic Acid (RNA)
• Strategic Thinking
• Technical Writing
• Ultra Performance Liquid Chromatography (UPLC)

• Current employees apply.
• Contingent workers apply.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other legally protected characteristics. As a federal contractor, we comply with affirmative action requirements for protected veterans and individuals with disabilities.

For more information about personal rights under U.S. Equal Opportunity Employment laws, visit the EEOC and related resources.

Salary Range: $ – $. The successful candidate will be eligible for annual bonus and long‑term incentive, if applicable. We offer a comprehensive package of benefits, including medical, dental, vision, retirement (401(k)), paid holidays, vacation and sick days.

Apply through the company website. The Final date to receive applications is stated on the posting.