Sr. Supervisor, Manufacturing (Night shift)
Biogen
August 24, 2026
On-site
Triangle, NC
Operations
About This Role
This position is on a 12-hour rotation, Red Night shift on a 2, 2, 3 schedule.
Responsibilities
- Supervise Manufacturing Associates on a Night shift: observe/instruct, coach, lead, and develop staff; identify development gaps and implement plans.
- Perform manufacturing activities per cGMPs, ensuring reports are fully trained on an activity prior to performing it.
- Schedule and direct daily manufacturing activities; timely communicate scheduling changes/issues to staff and management.
- Coordinate manufacturing activities with other departments (e.g., production schedulers, quality control, materials management, manufacturing sciences, validation, facilities, process engineering, quality assurance) to ensure execution of PPRs, sampling, validation, etc.
- Review and approve batch-related documents, ensuring proper cGMP documentation practices.
- Train associates on process activities, including safety and cGMP requirements; review safety records and implement corrective measures.
- Supervise validation activities to ensure timely execution of required validation protocols.
- Troubleshoot operational/equipment problems; coordinate emergency repairs, changeovers, and preventative maintenance with facilities.
- Coordinate and draft revisions of batch-related documents, including batch records and SOPs.
Qualifications/Skills
- Grounded understanding of parenteral filling and drug product manufacturing principles; solid knowledge of engineering/scientific principles for assigned areas.
- Particularly knowledgeable in safety, GMP, and Human Performance principles.
- Leadership, organization, accountability, and tactical resource allocation.
- Experience in a GMP pharmaceutical manufacturing facility.
Required Skills/Education
- Sr. Supervisor: Bachelor’s (STEM strongly preferred) + 4 years transferrable experience; or Associates + 6 years; or High School + 8 years.
Preferred Skills
- Technical/practical experience in Drug Product/Parenteral Filling.
- Competency in electronic systems (Oracle, CMMS, Trackwise, etc.).
Benefits (if applicable as stated)
- Base compensation range: $98,000.00–$127,000.00.
- Medical, dental, vision, life; fitness/wellness reimbursement; short- and long-term disability; paid vacation and end-of-year shutdown; paid holidays/personal days; sick time; paid maternity/parental leave; 401(k) match; employee stock purchase plan; tuition reimbursement up to $10,000/year; employee resource group participation.
This position is on a 12-hour rotation, Red Night shift on a 2, 2, 3 schedule.
Responsibilities
- Supervise Manufacturing Associates on a Night shift: observe/instruct, coach, lead, and develop staff; identify development gaps and implement plans.
- Perform manufacturing activities per cGMPs, ensuring reports are fully trained on an activity prior to performing it.
- Schedule and direct daily manufacturing activities; timely communicate scheduling changes/issues to staff and management.
- Coordinate manufacturing activities with other departments (e.g., production schedulers, quality control, materials management, manufacturing sciences, validation, facilities, process engineering, quality assurance) to ensure execution of PPRs, sampling, validation, etc.
- Review and approve batch-related documents, ensuring proper cGMP documentation practices.
- Train associates on process activities, including safety and cGMP requirements; review safety records and implement corrective measures.
- Supervise validation activities to ensure timely execution of required validation protocols.
- Troubleshoot operational/equipment problems; coordinate emergency repairs, changeovers, and preventative maintenance with facilities.
- Coordinate and draft revisions of batch-related documents, including batch records and SOPs.
Qualifications/Skills
- Grounded understanding of parenteral filling and drug product manufacturing principles; solid knowledge of engineering/scientific principles for assigned areas.
- Particularly knowledgeable in safety, GMP, and Human Performance principles.
- Leadership, organization, accountability, and tactical resource allocation.
- Experience in a GMP pharmaceutical manufacturing facility.
Required Skills/Education
- Sr. Supervisor: Bachelor’s (STEM strongly preferred) + 4 years transferrable experience; or Associates + 6 years; or High School + 8 years.
Preferred Skills
- Technical/practical experience in Drug Product/Parenteral Filling.
- Competency in electronic systems (Oracle, CMMS, Trackwise, etc.).
Benefits (if applicable as stated)
- Base compensation range: $98,000.00–$127,000.00.
- Medical, dental, vision, life; fitness/wellness reimbursement; short- and long-term disability; paid vacation and end-of-year shutdown; paid holidays/personal days; sick time; paid maternity/parental leave; 401(k) match; employee stock purchase plan; tuition reimbursement up to $10,000/year; employee resource group participation.