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Principal Scientist, Pharmaceutical Analytical Sciences

Job in Rahway, Union County, New Jersey, 07065, USA
Listing for: Merck
Full Time position
Listed on 2026-07-27
Job specializations:
  • Pharmaceutical
    Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 150000 - 190000 USD Yearly USD 150000.00 190000.00 YEAR
Job Description & How to Apply Below



Job Description

Principal Scientist, Pharmaceutical Analytical Sciences
The Pharmaceutical Analytical Sciences (PAS) team at our company has an exciting opportunity for a Principal Scientist based in Rahway, NJ. Join us and experience our culture firsthand - 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.



Job Description

Principal Scientist, Pharmaceutical Analytical Sciences
The Pharmaceutical Analytical Sciences (PAS) team at our company has an exciting opportunity for a Principal Scientist based in Rahway, NJ. Join us and experience our culture firsthand - 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.

Driving Our Company s Pipeline
As a Principal Scientist, you will be part of a team developing innovative analytical methodologies for medicines based on small molecules, peptides, mRNA, oligonucleotides and bioconjugates. Our responsibilities range from early stage up to commercialization for both drug substance and a broad array of drug product dosage forms, including oral, sterile and combination products. You will lead and make critical contributions to the development of drug product and process through analytical characterization, imaging tools and data analysis.

You will also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities, in not particular order and by no means complete, include:

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