Senior QC Chemist — Capillary Electrophoresis (GMP)

BeiGene, Ltd.; Hopewell (VA); On-site; USD 91,000 - 126,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401(k)

FSA/HSA

Life Insurance

Paid Time Off

Wellness

Job summary

BeOne Medicines Ltd. is seeking an experienced QC Chemistry professional to perform capillary electrophoresis-based testing to support GMP manufacturing, testing, and release of material, intermediates, and finished products.

You will review data, report results, and lead troubleshooting for CE-related methods. The role requires a 4+ year track record in FDA-regulated biotech/pharma, familiarity with USP/EP and cGMP/EU GMP, and hands-on instrument validation experience.

Qualifications

• Bachelor's or above in Chemistry, Biochemistry, or Biotechnology related scientific discipline.
• Minimum 4+ years of working experience in an FDA-regulated biotechnology/pharmaceutical company.
• Familiar with USP/EP and cGMP/EU GMP regulations.
• Experience with HPLC, GC, TOC, and Capillary Electrophoresis techniques.

Responsibilities

• Perform routine and non-routine testing using capillary electrophoresis techniques in the QC Chemistry laboratory.
• Review, interpret, and report analytical data in accordance with GMP regulations.
• Lead troubleshooting efforts for analytical methods and instrumentation related to CE.
• Conduct laboratory investigations including OOS and deviations.

Skills

Capillary electrophoresis

GMP compliance

Data analysis

Troubleshooting CE

Method validation

OOS investigations

Education

Bachelor's in Chemistry/Biotech

Tools

Waters Empower

Job description

BeOne Medicines Ltd. is seeking an experienced QC Chemistry professional to perform capillary electrophoresis-based testing to support GMP manufacturing, testing, and release of material, intermediates, and finished products.

You will review data, report results, and lead troubleshooting for CE-related methods. The role requires a 4+ year track record in FDA-regulated biotech/pharma, familiarity with USP/EP and cGMP/EU GMP, and hands-on instrument validation experience.