Analyst, Qc Microbiology – Product Testing

beigene.at

$79,000.00 - $109,000.00 annually; bonus/equity: e...
Not specified
Qc microbiology laboratory testing
Utilities sampling
Environmental monitoring
BeiGene is seeking an experienced Analyst in QC Microbiology to support GMP manufacturing and testing of pharmaceutical products. The ideal candidate should have a strong background in microbiological testing and experience working in an FDA-regulated environment

Job Summary

  • Performs laboratory activities to support GMP manufacturing, testing and release of materials, intermediates, and finished products under FDA/EU regulations.
  • Perform QC Microbiology laboratory testing including bioburden, endotoxin, sterility, and microbial ID testing to ensure timely generation and reporting of test results.
  • The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

Matching Summary

Match Score: 85

BeiGene is seeking an experienced Analyst in QC Microbiology to support GMP manufacturing and testing of pharmaceutical products. The ideal candidate should have a strong background in microbiological testing and experience working in an FDA-regulated environment.

Salary

$79,000.00 - $109,000.00 annually; Bonus/Equity: eligible for annual bonus plan and discretionary equity awards; Benefits: comprehensive benefits package

Skills & Requirements

Must-have

  • QC Microbiology laboratory testing
  • utilities sampling
  • environmental monitoring
  • cGMP/EU GMP regulations
  • microbiological testing methods

Nice-to-have

  • scientific and business professionals
  • collaborative
  • passionate interest in fighting cancer
  • hands-on approach
  • can do attitude

Key Requirements

  • Bachelor’s Degree or above in Microbiology, Biology or Biotechnology
  • Minimum of 2 years of working experience
  • 5+ years of experience preferred with no higher education
  • Working knowledge and experience with microbiological testing methods
  • Familiar with USP/EP and cGMP/EU GMP regulations
  • Familiar with instrument and equipment validation

Work Rights

Not specified

Tailored Resume

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