Principal Scientist, Pharmaceutical Analytical Sciences

Merck; Rahway (NJ); On-site; USD 150,000 - 190,000; Full time

Job summary

Merck in Rahway, NJ seeks a Principal Scientist to drive the development of analytical methodologies for medicines across small molecules, peptides, mRNA, oligonucleotides and bioconjugates.

You will lead analytical characterization, imaging tools and data analysis to support drug product and process development from early stage through commercialization, contributing to regulatory submissions to enable clinical trials.

Job description

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: