Sr Associate I, Quality Control Microbiology

Biogen

Research Triangle Park, NC, United States
Base: $81,000.00-$105,000.00; bonus/equity: short ...
Onsite
Microbiological testing
Environmental monitoring
Aseptic techniques
The Sr. Associate I is responsible for leading key operational aspects of the QC Microbiology laboratory, performing and training team members on microbial testing of in-process drug substance, EM/UM, and raw materials samples

Job Summary

  • The Sr. Associate I is responsible for leading key operational aspects of the QC Microbiology laboratory, performing and training team members on microbial testing of in-process drug substance, EM/UM, and raw materials samples.
  • This onsite position operates on 10-hour shifts from Sunday through Wednesday during the first shift (8AM-6PM), with some occasional support required outside of those hours.
  • Biogen offers a full and highly competitive range of benefits designed to support employees’ and their families physical, financial, emotional, and social well-being.

Matching Summary

The Sr. Associate I is responsible for leading key operational aspects of the QC Microbiology laboratory, performing and training team members on microbial testing of in-process drug substance, EM/UM, and raw materials samples.

Salary

Base: $81,000.00-$105,000.00; Bonus/Equity: short term and long-term incentives, cash bonus and equity incentive opportunities; Benefits: Medical, Dental, Vision, & Life insurances, Fitness & Wellness programs, Disability insurance, paid vacation, holidays, sick time, Maternity and Parental Leave, 401(k) program, Employee stock purchase plan, Tuition reimbursement

Skills & Requirements

Must-have

  • microbiological testing
  • environmental monitoring
  • aseptic techniques
  • LIMS experience
  • cleanroom gowning requirements

Nice-to-have

  • collaborative approach
  • attention to detail
  • data integrity commitment
  • pioneering spirit
  • inclusion and belonging

Key Requirements

  • Bachelor’s in Microbiology, Biology, or related field
  • Minimum 4 years’ experience
  • pharmaceutical microbiology GMP-regulated manufacturing
  • document control experience
  • fundamental statistical tools familiarity

Work Rights

Not specified

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