Clinical QC Analyst: Release & Stability (GMP)

Insight Global; Malvern (Chester County); On-site; USD 47,733 - 67,984; Full time

Benefits offered by this job

Comprehensive benefits package

401(k) retirement plan eligibility

Paid sick leave

Job summary

A leading staffing agency is seeking a QC CRS Analyst responsible for conducting biochemical and testing of drug materials. This role requires one year of GMP QC experience and a bachelor's degree in biology or chemistry. Key responsibilities include analytical testing, peer reviews, and supporting method validation. The position offers a competitive hourly wage and comprehensive benefits, including medical and 401(k) retirement plan eligibility after 90 days.

Qualifications

• Minimum one year of relevant GMP QC work experience in pharmaceutical lab.
• Proficient in the application of cGMP and GLP regulations.
• Familiarity with analytical technologies in Cell and Gene Therapy Laboratories.

Responsibilities

• Conduct analytical biological testing of drug products.
• Perform peer reviews and approvals of laboratory data.
• Support analytical method qualification and validation.

Skills

GMP QC experience

Flow Cytometry

Microsoft Office proficiency

Analytical testing

Technical document interpretation

Education

Bachelor's degree in biology or chemistry

Job description

A leading staffing agency is seeking a QC CRS Analyst responsible for conducting biochemical and testing of drug materials. This role requires one year of GMP QC experience and a bachelor's degree in biology or chemistry. Key responsibilities include analytical testing, peer reviews, and supporting method validation. The position offers a competitive hourly wage and comprehensive benefits, including medical and 401(k) retirement plan eligibility after 90 days.