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

Responsibilities

• 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

Requirements

• 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
• The following combination of academic and/or relevant experience may be considered: 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
• Additional Information
• The base compensation range for this role is: $98,000.00-$127,000.00
• Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
• Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
• In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being ; including, but not limited to:
• Medical, Dental, Vision, & Life insurances
• Fitness & Wellness programs including a fitness reimbursement
• Short- and Long-Term Disability insurance
• A 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 of up to $10,000 per calendar year
• Employee Resource Groups participation
• Why Biogen?
• At Biogen, we are committed to building on our culture of inclusion and belonging that

Benefits

Additional Information

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. Shift Details : This role follows a 2-2-3 calendar rotation on nights (6:00 PM - 6:00 AM ET) Internal Shift Details: Black Night rotating schedule We are seeking a Supervisor to lead night shift operations supporting drug substance manufacturing under cGMP conditions. This role oversees Manufacturing Associates, ensures compliant execution of production activities, and drives a culture of safety, quality, and continuous improvement. You will play a key role in coordinating cross-functional activities and delivering manufacturing campaigns in a highly regulated environment.

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