Sr. Supervisor, Manufacturing - Media & Solution Preparation (Nights)

About This Role Our factories run 24/7 operations. Our manufacturing teams work 12‑hour shifts (either Days or Nights) on a 2-2-3 calendar rotation. This role follows a 2-2-3 calendar rotation on nights (6:00 PM – 6:00 AM ET). Black Night rotating schedule. What You’ll Do Manage, coach, and develop Manufacturing Associates; identify skill gaps and implement development plans. Schedule and direct daily manufacturing operations, ensuring alignment with production timelines and priorities. Ensure all activities are executed in compliance with cGMP standards and that team members are fully trained prior to execution. Partner cross‑functionally with QC, QA, Materials Management, MS&T, Validation, Facilities, and Engineering to support batch execution, sampling, and validation activities. Lead and support training efforts across safety, GMP, and process‑related activities; monitor and improve safety performance. Troubleshoot operational and equipment issues; coordinate maintenance, repairs, and changeovers with Facilities. Draft and revise manufacturing documentation, including batch records and SOPs. Who You Are You’re a hands‑on leader with a strong foundation in drug substance manufacturing and a deep understanding of cGMP operations. You bring both technical credibility and people leadership, with the ability to influence, coach, and drive results in a fast‑paced manufacturing environment. Required Skills Bachelor’s degree from an accredited college or university, STEM preferred and at minimum 3 years of direct experience. A BioWorks Certificate and/or associate’s degree, STEM preferred and at minimum 5 years of direct experience. A High School Diploma (or equivalent) and at minimum 7 years of direct experience. Strong working knowledge of cGMP requirements with the ability to ensure compliant execution of manufacturing activities. Demonstrated experience being a lead, leading, supervising, coaching, and/or developing manufacturing teams. Experience leading training efforts across safety, GMP, and process‑related activities, with a focus on compliance and performance. Preferred Skills Experience troubleshooting operational and equipment issues and coordinating maintenance, repairs, and changeovers. Experience drafting and revising manufacturing documentation, including batch records and SOPs. Job Level Professional Benefits 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 an additional end‑of‑year 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. EEO Statement 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. #J-18808-Ljbffr Biogen, Inc.