Job Description About This Role

　　The Manager, Quality Control (QC) – Sample Control oversees the responsibilities of the QC Sample Control group at the Research Triangle Park sites; develops team members and career paths; implements best industry practices; leads and participates in projects and participates in cross-site teams. Ensures team is aligned with goals, objectives. Schedules/balances team workload with respect to assignments, responsibilities, personnel, management of departmental milestones. Accountable for approval of technical documents for QC team. Responsible for ensuring GMP compliance, and alignment with quality systems.

　　What You’ll Do

　　Oversee team deliverables and sustainability with timely communication for priorities. Properly escalate issues to senior QC management as applicable to impact for teams.Able to flex and respond to unexpected situations, demands. Effectively problem solve and reallocate resources as necessary.Provide leadership for QC initiatives as related to scientific, technical discipline, business strategy- global improvements. Lead more complex projects, initiatives.  Manage activities including technical writing, project representation that are complex and/or those with significant impact.Hire and develop a well-functioning team – focusing on values and culture. Ensure establishment of goals and development plans for employees. Ensure effective team training for group activities, responsibilities and perform performance reviews.Coordinate activities with other departments; provide updates to QC team mgmt.  Routinely work closely with Quality Assurance, Stability, Regulatory, TD, Validation, AT, cross site stakeholders etc.

　　Who You Are

　　You love collaborating cross functionally to determine root cause and potential corrective actions.  You enjoy motivating and developing a team to meet or exceed goals.

　　Qualifications Bachelor's degree in science.5 years of experience in GMP in a Quality role, laboratory role, or support role.A mimimum of 2 years of leadership experience in comparable role, experience with regulations, FDA/MHRACan effectively lead change & complete initiatives aligned with the business.Ability to flex and respond to unexpected situations, demands. Additional Information

　　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.