Sr Associate I, Quality Control Microbiology

Schedule

This onsite position operates on 10‑hour shifts from Sunday through Wednesday during the first shift (8AM‑6PM), with occasional support required outside of those hours.

We are seeking a highly motivated QC Microbiology Sr Associate I to support microbiological testing of in‑process and raw materials, and environmental/utilities monitoring at an RTP drug substance manufacturing facility. The Sr. Associate I is responsible for leading key operational aspects of the QC Microbiology laboratory, performing and training other team members on the microbial testing of all in‑process drug substance, EM/UM, and raw materials samples.

Additionally this role is responsible for method qualification and projects as assigned.

• Review test data in LIMS
• Prepare quarterly EM/UM reports
• Support testing for all qualification and study directed testing
• Troubleshoot complex assays
• Perform microbiology testing (e.g., Bioburden, Endotoxin, plate reading, and microbial identification) following standard procedures
• Conduct routine Environmental Monitoring (viable and non‑viable) in controlled manufacturing areas
• Collect and process utility and compressed gas samples
• Comply with SOPs and controlled documents under minimal supervision
• Maintain laboratory cleanliness, equipment readiness, and inventory
• Perform investigations (i.e., laboratory and deviations)
• Follow site safety and contamination control policies
• Work overtime as required by business needs
• Perform other assigned duties

Someone who demonstrates strong attention to detail and analytical skills, along with a solid commitment to maintaining data integrity and quality. You possess a collaborative approach and work effectively across manufacturing and facilities teams.

• Bachelor’s in Microbiology, Biology, or related field
• Minimum 4years’ experience in pharmaceutical microbiology and GMP‑regulated manufacturing
• LIMS experience, including using electronic notebooks
• Demonstrated knowledge of microbiological assays (bioburden, endotoxin, environmental monitoring), aseptic techniques, and general laboratory techniques
• Experience with document control including reviewing and editing technical documents
• Intermediate familiarity with fundamental statistical tools to analyze data in relation to trends and results
• Ability to follow procedures and complete technical tasks
• Can meet cleanroom and aseptic gowning requirements
• Physically able to stand long periods, bend, move carts, and lift 25lbs
• Strong written and verbal communication skills, along with proficiency in Microsoft Word and Excel
• Excellent organizational skills with the ability to prioritize, follow through on tasks, and meet deadlines

• Advanced knowledge of Microbiology testing and Microbiology theory
• Prior experience in utilities monitoring, including gas monitoring
• Prior training experience, including classroom training
• Proficient in using LIMS systems, Veeva, Kneat, and Microsoft software
• Knowledgeable in GMP, GLP, and GDP requirements
• Advanced knowledge of all compendial test methods (Bioburden, Endotoxin, Sterility testing)
• LEAN lab and Six Sigma training and/or certification
• Advanced experience with microbial , ability to troubleshoot complex equipment and instrumentation (MALDI, Micro Seq)
• Experience performing EM/UM excursion investigations

Professional

• Base salary range: $81,000.00 – $
• Short‑term and long‑term incentives, including cash bonus and equity incentive opportunities
• Medical, Dental, Vision, & Life insurances
• Fitness & Wellness programs including a fitness reimbursement
• Short‑ and Long‑Term Disability insurance
• Minimum of 15 days of paid vacation and additional shutdown time off (Dec
  26‑Dec
  31)
• Up to 12 company paid holidays + 3 paid days off for Personal Significance
• 80 hours of sick time per calendar year
• Paid Maternity and Parental Leave benefit
• 401(k) program participation with company matched contributions
• Employee stock purchase plan
• Tuition reimbursement up to $10,000 per calendar year
• Employee Resource Groups participation

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E‑Verify Employer in the United States.