Senior Scientist I or Scientist III - Analytical Chemist (Drug Product) - FSP

Parexel•United States-New Jersey-Remote, NJ

40d•Onsite

About The Position

Parexel FSP is seeking a Scientist 3 or Senior Scientist I - Analytical Chemist (Drug Product) to work as a full-time employee on a long-term assignment onsite at one of their clients in Rahway, NJ. This role involves supporting the development and delivery of new therapies within the CMC Operations group. The position requires a strong background in analytical chemistry, particularly in a GMP laboratory environment, with a focus on drug product analysis. The ideal candidate will be adept at chromatographic techniques, documentation, and project management, contributing to the development of therapies that benefit patients.

Requirements

B.S./M.S. in Chemistry, Chemical Engineering, Biochemistry, Biology or similar life sciences.
Relevant years of experience as listed below in a GMP laboratory environment.
Scientist 3 - B.S. with 3-5 years of experience; M.S. with 1-2 years of experience
Senior Scientist - B.S. with 5+ years of experience; M.S. with 2+ years of experience
Hands-on experience with chromatographic analysis using various UPLC, HPLC and GC techniques, including method and instrument troubleshooting.
Consistently adheres to GDP standards with accurate, compliant documentation.
General knowledge of separations science.
General understanding of analytical method development and method validation.
Hands-on experience with FTIR, KF and Dissolution.
Strong computer, scientific, and organizational skills.
Excellent communication (oral and written) and attention to detail.
Excellent organization to multi-task and manage multiple ongoing projects in parallel including GMP release, stability testing along with data processing, interpretation and reporting.
Ability to work independently and as part of a team, displaying self-motivation, adaptability, and a positive attitude.

Nice To Haves

Empower software
Analysis of drug product and drug substance

Responsibilities

Perform hands-on experience with chromatographic analysis using various UPLC, HPLC and GC techniques.
Method and instrument troubleshooting.
Accurate, compliant documentation adhering to GDP standards.
Analytical method development and method validation.
Hands-on experience with FTIR, KF and Dissolution.
Multi-task and manage multiple ongoing projects in parallel including GMP release, stability testing along with data processing, interpretation and reporting.
Work independently and as part of a team, displaying self-motivation, adaptability, and a positive attitude.