Scientist - II

Summary

The Merck Small Molecule Analytical Research and Development group is seeking a dedicated Scientist to join our GMP operations team in Rahway, NJ. This role is ideal for a high-energy professional with a passion for exceptional science and a commitment to improving human health through innovative drug delivery. You will join a diverse team characterized by strong ethics and integrity, focusing specifically on the critical task of releasing clinical supplies for new and ongoing studies.

This is a hands‑on, lab‑based position that offers the opportunity to work with advanced predictive analytical tools in a fast‑paced, collaborative environment.

• Execute Good Manufacturing Practices (GMP) activities, including release and stability testing for active pharmaceutical ingredients (APIs) and pharmaceutical formulations.
• Utilize advanced analytical techniques such as HPLC, UPLC, and Dissolution testing to support clinical supply development.
• Document all experimental procedures, results, and conclusions with high precision, adhering strictly to ALCOA principles and Good Documentation Practices (GDP).
• Troubleshoot and investigate technical challenges in the lab through active collaboration with cross‑functional project teams and Quality stakeholders.
• Validate and implement robust analytical methods to ensure the integrity of clinical materials.
• Manage data integrity by performing accurate data entry, thorough data review, and authoring technical reports or data summaries.
• Collaborate effectively with colleagues in Process Chemistry, Pharmaceutical Operations, and Global Development Quality to meet project milestones.
• Maintain a high level of independence in lab operations while contributing to a cohesive team environment.

• Bachelor of Science (B.S.) in Chemistry, Pharmaceutical Sciences, or a related Life Science field with 3–5 years of relevant industry experience.
• Master of Science (M.S.) in Chemistry, Pharmaceutical Sciences, or a related Life Science field with 2 years of relevant industry experience.

• Core Technical
  
  Skills:
  
  Hands‑on experience with HPLC, UPLC, Dissolution testing, spectroscopy, and advanced chromatographic separations.
• Software Proficiency:
  Practical experience using Empower software for data acquisition and analysis.
• Regulatory Knowledge:
  Deep understanding of GMP operations, GDP, and ALCOA documentation standards.
• Analytical Breadth:
  Experience with LCMS and data science applications is highly preferred; experience with Gas Chromatography (GC) is a plus.
• Soft Skills:
  
  Proven ability to troubleshoot independently, high attention to detail, and excellent verbal and written communication skills.
• Stability: A consistent and stable job history within a GMP or pharmaceutical laboratory setting is required.

• Location:
  
  This is a 100% onsite, lab-based role located in Rahway, NJ.
• Position Type:
  Temporary assignment with the possibility of extension based on performance and business needs.
• Work Environment:
  Requires a team-oriented "hard worker" who is curious, independent, and capable of operating without constant hand-holding.