Senior Scientist, Small Molecule - Analytical R&D GMP Labs

Merck • Rahway, NJ

4d • $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, diversified 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 a Senior 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.

Requirements

• Excellent written and oral communication skills, as well as interpersonal skills, are necessary to qualify for this role. Candidates will also be required to work in a team environment with cross-functional interactions.

Nice To Haves

• Though not required, the ideal applicant would have hands-on experience in GMP operations, advanced chromatographic separation science, spectroscopy analysis, dissolution testing, and other analytical techniques.
• In addition, experience with Empower, data science, and LCMS are also a plus.

Responsibilities

• Support execution of Good Manufacturing Practices (GMP) activities such as release and stability testing to support development of active pharmaceutical ingredients (APIs), pharmaceutical formulations, and manufacturing processes using both traditional and advanced analytical tools.
• Document the execution, procedure, results, and conclusions of experiments in a detailed and organized manner following ALCOA principles.
• Troubleshoot and investigate any challenges associated with the GMP testing through active collaboration with cross-functional project teams and/or Quality stakeholders.
• Validate and implement analytical methods to support release and stability testing of clinical materials.
• Perform data entry, data review, and author analytical reports or data summaries.
• Strong collaboration with fellow Analytical Research & Development colleagues as well as cross-functional partners such as Global Development Quality, Process Chemistry, and Pharmaceutical Operations.
• Support compliance audit/inspection activities.

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.

What This Job Offers

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