Analytical Chemist - Chromatography Focus (GLP)

Parexel International; Pennsylvania; On-site; USD 90,000 - 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 III - Analytical Chemist (Chromatography Focus) for a full-time, long-term assignment onsite at a client site in West Point, PA. The role supports GLP analytical testing, data interpretation, and compliant documentation across multiple therapeutic areas.

The candidate will manage samples, execute HPLC analyses, write reports, and ensure inspection readiness. A relevant chemistry degree with 3–5 years (or a Master with 1–2 years) of experience is required.

Qualifications

• Bachelor's degree in chemistry with 3–5 years of relevant experience or a Master's with 1–2 years of relevant experience.
• Experience supporting GLP analytical testing and documentation.
• Familiarity with ALCOA principles and compliant data handling.

Responsibilities

• Manage non-clinical study samples including receipt, tracking, organization, and documentation.
• Support GLP activities and dose formulation analysis using HPLC and related techniques.
• Document procedures, execution, results, and conclusions with ALCOA-compliant records.
• Troubleshoot GLP testing issues collaborating with cross-functional teams and QA.
• Perform data entry/review and author analytical reports and summaries.
• Support audit/inspection readiness and ensure traceable, accurate work.
• Assist in maintaining a compliant, safe, and inspection-ready laboratory.

Skills

GLP compliance

ALCOA

HPLC analysis

Data interpretation

Communication

Team collaboration

Education

Bachelor's degree in chemistry

Master's degree in chemistry

Tools

Empower software

Job description

Parexel is seeking a Scientist III - Analytical Chemist (Chromatography Focus) for a full-time, long-term assignment onsite at a client site in West Point, PA. The role supports GLP analytical testing, data interpretation, and compliant documentation across multiple therapeutic areas.

The candidate will manage samples, execute HPLC analyses, write reports, and ensure inspection readiness. A relevant chemistry degree with 3–5 years (or a Master with 1–2 years) of experience is required.