Senior Analytical Chemist - GMP Stability & Method Dev

Parexel; Montpelier (VT); On-site; USD 85,000 - 120,000; Full time

Benefits offered by this job

Full benefits

401K

Paid time off

Job summary

Parexel is seeking a Scientist 3 - Analytical Chemist (Drug Substance Analysis) to join the drug product stability testing lab onsite in Rahway, NJ. This full-time position includes comprehensive benefits and long-term assignment with Parexel FSP.

The candidate will perform routine and stability analyses, develop and validate methods, and document findings in a GMP-compliant environment for late-stage development and testing.

Qualifications

• BS or MS in a life sciences field with GMP laboratory experience.
• Experience with chromatographic analysis and method validation.
• Proven ability to document with GDP standards and audit-ready reports.

Responsibilities

• Perform routine and stability sample analysis in a GMP lab.
• Author SOPs and contribute to method development and validation.
• Process and interpret data; prepare reports supporting product development.
• Maintain quality documentation and support release and stability testing.

Skills

Chromatographic analysis

GDP compliance

Separation science

Analytical method development

FTIR

KF

Dissolution

Data processing

Attention to detail

Multi-tasking

Independent work

Team collaboration

Education

BS in Chemistry / Chemical Engineering / Biochemistry / Biology or related

MS in Chemistry or related (preferred)

Tools

Empower software

HPLC/UPLC/GC instrumentation

Job description

Parexel is seeking a Scientist 3 - Analytical Chemist (Drug Substance Analysis) to join the drug product stability testing lab onsite in Rahway, NJ. This full-time position includes comprehensive benefits and long-term assignment with Parexel FSP.

The candidate will perform routine and stability analyses, develop and validate methods, and document findings in a GMP-compliant environment for late-stage development and testing.