Biologics Manufacturing Supervisor

About the role

AbbVie is looking for a Biologics Manufacturing Supervisor to lead and guide a stream-specific biologics group in manufacturing clinical and bulk drug substances according to safety, regulatory and operational requirements. The supervisor supports Cell Culture, Purification or Central Services areas and works in the Biologics Production facility.

Key responsibilities

• Ensure performance metrics and workload deliverables are completed in line with the site's business model, and build collaborative relationships with colleagues and departments.
• Organize daily and weekly shift activities and direct shift personnel.
• Coordinate stream and cross-stream initiatives, drive process troubleshooting, assist with change implementation and CAPAs, and resolve project hurdles.
• Operate computerized systems such as MES, HMI and PLC.
• Supervise manufacturing of bulk drug substance under cGMP, oversee batch records and SOPs, review records for completeness and accuracy, and act as point of contact for audits.
• Maintain a safe work environment in line with EHS policies and keep the plant audit-ready.
• Recruit, retain and develop manufacturing personnel and set a positive team environment.

Required profile

• Bachelor's or Master's degree in a science, pharmacy or engineering field, or equivalent.
• Minimum 5 years of experience in biotechnology or pharmaceutical manufacturing.
• Minimum 2 years of supervisory experience in biotechnology or pharmaceutical manufacturing.
• Ability to work with minimal management direction and strong organizational skills.

Required skills

• Working knowledge of safety, quality systems and cGMP.
• Knowledge of complex technical issues and manufacturing experience in a biopharmaceutical or similar environment.
• Computer proficiency and scheduling experience; good writing skills.