Analytical Chemist (Drug Product) – GMP & Stability

Parexel; Lansing (MI); On-site; USD 85,000 - 125,000; Full time

Benefits offered by this job

Full benefits

Sick time

401K

Paid holidays

Paid time off

Job summary

Parexel is seeking a Scientist 2 or 3 - Analytical Chemist (Drug Product) for a full-time role, onsite at a client site in Rahway, NJ. The position supports drug product stability testing and analytical characterization with a focus on compliance and data integrity.

The candidate will perform routine and stability analyses, SOP authoring, and problem solving while contributing to continuous improvement and the adoption of new technologies in a regulated lab environment.

Qualifications

• Experience with GMP analysis using HPLC/UPLC including assay/impurity, troubleshooting and data processing interpretation/analysis.
• Routine testing, data integrity assessments, investigative report authoring, and/or sample management responsibilities.
• Strong computer, scientific, and organizational skills.
• Clear communicator who speaks up about problems and improvement ideas.
• Able to manage multiple ongoing projects.
• Ability to work independently and as part of a team.
• Self-motivation, efficiency, adaptability, and a positive attitude.

Responsibilities

• In the drug product registration stability testing lab, you’ll perform routine and stability sample analysis, SOP authoring, and day-to-day problem solving.
• You’ll contribute to new technologies and continuous improvement measures for optimized lab operations and other testing requirements.
• You’ll apply analytical characterization technologies and compliance principles to drive method robustness and high-quality stability data.

Skills

GMP analysis

HPLC/UPLC

data interpretation

multitasking

team collaboration

independent work

self-motivation

Education

BS/MS in Chemistry

Tools

Empower software

Job description

Parexel is seeking a Scientist 2 or 3 - Analytical Chemist (Drug Product) for a full-time role, onsite at a client site in Rahway, NJ. The position supports drug product stability testing and analytical characterization with a focus on compliance and data integrity.

The candidate will perform routine and stability analyses, SOP authoring, and problem solving while contributing to continuous improvement and the adoption of new technologies in a regulated lab environment.