Scientist, Large Molecule Analytical (On-site)

MSD • Rahway, NJ

3d • $87,300 - $137,400 • Onsite

About The Position

The Large Molecule Analytical department within the Research & Development Division is seeking a laboratory-based Scientist to solve complex analytical problems at the interface of biology, chemistry, and laboratory informatics, supporting development of biologics drug substances and drug products. The successful candidate will collaborate in a fast-paced, integrated, multidisciplinary team.

The Scientist will develop, qualify, implement, troubleshoot, and transfer analytical methods for monoclonal proteins and other complex therapeutic proteins. The role calls for effective organizational, multitasking, and oral and written communication skills, scientific leadership, and an interest in conducting research and publishing. Experience with cross-functional collaboration in an academic or industrial setting is preferred.

The position is based primarily in Rahway, New Jersey, and is an on-site role. It is a regular employee position with a first-shift schedule and 10% travel. Domestic relocation is available; visa sponsorship is not available.

Requirements

• Bachelor of Arts or Bachelor of Science in analytical chemistry, biochemistry, or a related field, with at least 3 years of pharmaceutical industry experience; or a master's degree with at least 0 years of relevant experience, with expected graduation no later than January 2027.
• Prior experience in a laboratory environment.
• Ability to apply basic scientific principles and concepts to laboratory work.
• Ability to operate and troubleshoot analytical methods.
• Understanding of the fundamentals of separations science.
• Experience with UPLC/HPLC analysis of biologics (such as SEC, RP, or IEX) and CE techniques, or experience with molecular biology techniques (such as PCR and DNA extraction) and immunoassay techniques (such as ELISA and gel electrophoresis).
• Ability to manage prioritization and execution of individual deliverables within overall project timelines, with appropriate supervision.
• Demonstrated experience working in collaborative team environments.
• Experience authoring and reviewing internal technical reports, sections of regulatory filings such as INDs or BLAs, and external scientific publications.

Nice To Haves

• Experience working as part of a project team.
• Strong knowledge of protein structure and degradation pathways.
• Experience analyzing biologic modalities such as monoclonal antibodies, antibody-drug conjugates, and fusion proteins.
• Background in analytical methodologies and a sound scientific understanding of Critical Quality Attributes, QbD, and DOE principles.
• Experience with Microsoft Office and research applications such as RLIMS, ELN, and Empower.
• Experience in data analytics, programming, or laboratory automation.
• Evidence of strong cross-functional collaboration in an academic or industrial setting.

Responsibilities

• Solve complex analytical problems at the interface of biology, chemistry, and laboratory informatics to enable development of biologics drug substances and drug products.
• Develop, qualify, implement, troubleshoot, and transfer analytical methods for monoclonal proteins and other complex therapeutic proteins.
• Execute routine laboratory experiments and interpret data with appropriate technical guidance.
• Work within project timelines to prioritize and complete individual deliverables under appropriate supervision.
• Collaborate effectively in an integrated, multidisciplinary team environment.
• Author and review internal technical reports, sections of regulatory filings such as INDs and BLAs, and external scientific publications.

Benefits

• Medical, dental, vision, healthcare, and other insurance benefits for employees and their families.
• Retirement benefits, including a 401(k).
• Paid holidays.
• Vacation.
• Compassionate and sick days.
• Eligible for an annual bonus and long-term incentive, if applicable.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level