Job DescriptionMonday-Thursday, 10 hours (base) with occasional overtime and weekendsThis position is responsible for the supervision of manufacturing of clinical and commercial products under GMP conditions. The incumbent will supervise Manufacturing Associates on either a day, night, or hybrid shift; schedules shift tasks; ensures GMP compliance and safety; drafts and reviews manufacturing documents; troubleshoots; and coordinates with other departments.What You'll DoSupervises Manufacturing Associates - observing/instructing, coaching, leading and developing staff. Identifies technical/non-technical development gaps and implements applicable plans/objectives.Performs manufacturing activities per cGMPs, ensuring that reports are fully trained on a given activity prior to performing the activity.Schedules and directs daily manufacturing activities, timely communicating scheduling changes/issues to staff and management.Coordinates manufacturing activities with other departments. This includes providing updates to production schedulers, and working closely with quality control, materials management, manufacturing sciences, validation, facilities, process engineering, and quality assurance, etc. to ensure execution of PPRs, sampling, validation, etc.Reviews and approves batch related documents, ensuring the proper cGMP documentation practices are followed.Trains manufacturing associates on process activities, including Safety requirements and cGMP requirements. Reviews safety records and identifies/implements corrective measures.Supervises validation activities, ensuring proper and timely execution of validation protocols required in respective areas.Troubleshoots operational and equipment problems and makes recommendations. Also coordinates emergency repairs, changeovers, and preventative maintenance activities with the facilities group.Coordinates and drafts revisions of batch related documents, including batch records and SOPs.Who You AreGood understanding of the operating principles for large scale biologics manufacturing. Solid knowledge of the engineering and scientific principles associated with designated areas of responsibility. Understands the primary design principles for the facility (e.g. air pressure differentials, material flow, people flow, utility systems). Basic understanding of the roles of other functional groups within the company. Particularly knowledgeable on safety, GMP, and Human Performance principles.QualificationsRequired SkillsSr. SupervisorBachelor's Degree (BS) from an accredited college or university in a relevant scientific or engineering discipline with 6 years of relevant experience, or an Associate Degree in the scientific or engineering discipline with a minimum of 8 years relevant experience, or a high school degree with a minimum of 10 years relevant experience.Additional InformationAll your information will be kept confidential according to EEO guidelines.Why Biogen?Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients' lives and on changing the course of medicine. Together, we pioneer. Together, we thrive.At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.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.PDN-98a08a1f-4a04-4f9c-839f-e70d8cc8c80d