Drug Product Analytical Scientist – GMP & Stability

Parexel; United States; On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

Full benefits

Sick time

401K

Paid holidays

Paid time off

Job summary

Parexel is seeking a Scientist2 or Scientist3 for analytical chemistry in the drug product registration stability testing lab, onsite at West Point, PA. This is a full-time Parexel FSP position on long-term assignment with full benefits and 401(k).

The role requires hands-on GMP analytics using HPLC/UPLC, data integrity, and the ability to manage multiple projects in a compliant environment. Sponsorship is not offered.

Qualifications

• Experience with GMP analysis using HPLC/UPLC including assay/impurity, troubleshooting and data processing interpretation.
• 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

• Perform routine and stability sample analysis in the drug product registration lab.
• Author SOPs and contribute to day-to-day problem solving.
• Drive new technologies and continuous improvement for optimized lab operations.
• Support testing requirements and ensure high-quality stability data for late-stage development.

Skills

GMP/HPLC

Data interpretation

Data integrity

Communication

Project management

Teamwork

Self-motivation

Education

B.S./M.S. in Chemistry, Biochemistry, Engineering

Tools

Empower software

Job description

Parexel is seeking a Scientist2 or Scientist3 for analytical chemistry in the drug product registration stability testing lab, onsite at West Point, PA. This is a full-time Parexel FSP position on long-term assignment with full benefits and 401(k).

The role requires hands-on GMP analytics using HPLC/UPLC, data integrity, and the ability to manage multiple projects in a compliant environment. Sponsorship is not offered.