Sr. Supervisor, Manufacturing; Night shift

Position Overview

Apply for the Sr. Supervisor, Manufacturing (Night shift) role at Biogen. This role operates on a 12‑hour rotation with a Red Night shift on a 2‑2‑3 schedule. The position is responsible for supervising the manufacturing of clinical and commercial products under GMP compliance. You will oversee Manufacturing Associates, schedule shift tasks, review manufacturing documents, troubleshoot issues, and coordinate with multiple departments.

Key Responsibilities

• Supervise Manufacturing Associates by observing, instructing, coaching, and developing staff while identifying technical and non‑technical development gaps.
• Perform manufacturing activities in accordance with cGMP guidelines, ensuring proper training and adherence to processes.
• Schedule and direct daily manufacturing activities and communicate any changes or issues to staff and management.
• Coordinate manufacturing operations with departments such as quality control, materials management, manufacturing sciences, validation, facilities, process engineering, and quality assurance.
• Review and approve batch‑related documents to ensure proper cGMP documentation practices are followed.
• Train manufacturing associates on process activities, including safety and cGMP requirements, and review safety records to implement corrective measures.
• Supervise validation activities ensuring timely execution of required validation protocols.
• Troubleshoot operational and equipment problems, make recommendations, and coordinate emergency repairs, changeovers, and preventive maintenance.
• Coordinate and draft revisions of batch‑related documents, including batch records and SOPs.

Required Qualifications

• Demonstrated leadership that champions the correct behaviors and a values‐driven culture.
• Strong organizational skills with a commitment to maintaining a supportive work environment and team development.
• High degree of accountability with a clear understanding of roles, responsibilities, and expectations.
• Tactical resource allocation skills to manage tasks based on operational demands.
• Experience working in a GMP pharmaceutical manufacturing facility.
• Educational requirements: Bachelor's Degree (STEM strongly preferred) + 4 years of transferrable experience; or Associate’s Degree + 6 years; or High School Diploma (or equivalent) + 8 years of transferrable experience.

Preferred Qualifications

• Technical/practical experience in Drug Product/Parenteral Filling.
• Competency in electronic systems (Oracle, CMMS, Trackwise, etc.).

Benefits & Perks

• 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 leave.

Additional Information

• Compensation: Base compensation range for this role is $98,000.00–$ [range pending].
• Base salary is determined through an analytical approach utilizing relevant skills, experience, job location, and internal equity.
• Regular employees are eligible for short‑term and long‑term incentives, including cash bonus and equity incentive opportunities.