Sr. Scientist, Analytical R&D

MSD

6d•$117,000 - $184,200•Hybrid

About The Position

The Small Molecule Analytical Research and Development 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, experiences, exceptional science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. 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. You would also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities include: Driving solutions to analytical development challenges for synthetic small molecule, peptide and oligonucleotide active pharmaceutical ingredients and pharmaceutical products using conventional and novel technologies Designing scientific studies to inform the selection and deep understanding of synthetic routes, formulation compositions, and manufacturing processes. Implementing analytical methods for laboratory development, as well as release and shelf-life assessment of clinical supplies under good manufacturing practice (GMP) conditions. Providing leadership not only on drug development pipeline projects, but also innovative technology teams shaping analytical methods and tools of the future. Authoring regulatory submission documents across the project development lifecycle, as well as responding to agency questions. Documenting work in a detailed and timely manner. Collaborating effectively with internal and external partners. Presenting results of experiments and innovation efforts to project teams and at various cross-functional forums. Engaging in the external scientific community, e.g. through participation in professional organizations, conferences, and publications.

Requirements

Applicants must hold one of the following: 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.
A proven record of strong technical problem solving and innovative research experience, supported by scientific publications.
Excellent written and oral communication skills.
Strong leadership, collaboration and interpersonal skills.
Accountability
Adaptability
Analytical Method Development
Assay Development
Bioanalytical Analysis
Biochemical Assays
Cell-Based Assays
Chromatographic Techniques
Communication
GMP Environments
Innovative Thinking
Nuclear Magnetic Resonance (NMR) Analysis
Process Analytical Technology (PAT)
Strategic Thinking
Team Management
Technical Writing
Ultra Performance Liquid Chromatography (UPLC)

Nice To Haves

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

Responsibilities

Driving solutions to analytical development challenges for synthetic small molecule, peptide and oligonucleotide active pharmaceutical ingredients and pharmaceutical products using conventional and novel technologies
Designing scientific studies to inform the selection and deep understanding of synthetic routes, formulation compositions, and manufacturing processes.
Implementing analytical methods for laboratory development, as well as release and shelf-life assessment of clinical supplies under good manufacturing practice (GMP) conditions.
Providing leadership not only on drug development pipeline projects, but also innovative technology teams shaping analytical methods and tools of the future.
Authoring regulatory submission documents across the project development lifecycle, as well as responding to agency questions.
Documenting work in a detailed and timely manner.
Collaborating effectively with internal and external partners.
Presenting results of experiments and innovation efforts to project teams and at various cross-functional forums.
Engaging in the external scientific community, e.g. through participation in professional organizations, conferences, and publications.

Benefits

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.
More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

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