Analytical R&D Scientist — GMP (2nd Shift)

MSD

Rahway (NJ)

Sur place

USD 105 000 - 125 000

Plein temps

Il y a 3 jours
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Avantages offerts par ce poste

Medical benefits
Dental benefits
Vision benefits
401(k) plan
Paid holidays
Vacation

Résumé du poste

Merck & Co., Inc. in Rahway, NJ, seeks a Scientist in Analytical Chemistry to work on cross‑functional teams enabling small molecule, peptide, and oligonucleotide drug development through analytical characterization and data analysis.

This is a second‑shift role (3:30 PM–11:30 PM). You will support GMP release and stability testing, document experiments per ALCOA, troubleshoot challenges, and contribute to method validation and data reporting while collaborating with Quality, Process Chemistry,

Qualifications

  • Minimum 3 years relevant industry experience for applicants with a Bachelor degree in Chemistry, Pharmaceutical Sciences, or Life Sciences.
  • Experience with GMP operations and analytical method validation is preferred.
  • Strong written and oral communication and cross‑functional collaboration skills.

Responsabilités

  • Support GMP release and stability testing for APIs and formulations.
  • Document methodology, results, and conclusions following ALCOA principles.
  • Troubleshoot GMP testing with cross‑functional teams and Quality stakeholders.
  • Validate analytical methods for release and stability testing of clinical materials.
  • Generate and review analytical reports or data summaries.
  • Collaborate with Analytical R&D and Global Development Quality teams; support audits.

Connaissances

Analytical Chemistry
GMP
Data Review
Troubleshooting
Chromatography
Empower
LCMS

Formation

Bachelor of Science in Chemistry

Outils

Empower
LCMS
Spectroscopy

Description du poste

Merck & Co., Inc. in Rahway, NJ, seeks a Scientist in Analytical Chemistry to work on cross‑functional teams enabling small molecule, peptide, and oligonucleotide drug development through analytical characterization and data analysis.

This is a second‑shift role (3:30 PM–11:30 PM). You will support GMP release and stability testing, document experiments per ALCOA, troubleshoot challenges, and contribute to method validation and data reporting while collaborating with Quality, Process Chemistry,

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