Senior Analytical Chemist — GMP & Method Validation

Parexel; United States; On-site; USD 85,000 - 110,000; 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 to join as a full-time Parexel FSP employee on a long-term assignment onsite with a client in Rahway, NJ. The role focuses on chromatographic analysis, GMP documentation, and data reporting within a GMP laboratory.

The candidate should have hands-on LC/GC experience, method development knowledge, and familiarity with EMPOWER software or similar tools, with strong communication and teamwork skills.

Qualifications

• Hands-on chromatography experience with LC/GC
• Strong separations science knowledge
• GMP compliance and ALCOA documentation
• Excellent verbal and written communication
• Ability to multi-task and work in a team or independently

Responsibilities

• Support cleaning verification and swab analyses for GMP areas
• Perform raw materials release testing in GMP laboratory
• Support cleaning validation/verification for GMP manufacturing
• Interpret data, process, and report results
• Prepare GMP analytical reports and certificates of analyses
• Maintain safe, clean, and organized laboratory workspace
• Understand and apply analytical method development and validation concepts

Skills

LC/GC chromatography

Analytical method development

GMP/ALCOA documentation

Education

BS in Chemistry

MS in Analytical Chemistry

Tools

Empower chromatography software

Job description

Parexel is seeking a Scientist III - Analytical Chemist to join as a full-time Parexel FSP employee on a long-term assignment onsite with a client in Rahway, NJ. The role focuses on chromatographic analysis, GMP documentation, and data reporting within a GMP laboratory.

The candidate should have hands-on LC/GC experience, method development knowledge, and familiarity with EMPOWER software or similar tools, with strong communication and teamwork skills.