Job Description About This Role

　　The Head of Bio QA and Alliance Quality is a key member of the Site Leadership Team and​ has the overall responsibility for Global Quality Assurance operations at the RTP Bio site – including the Large Scale Manufacturing facility, Small Scale Manufacturing Facility, Flexible Volume Manufacturing, and Cell Banking operations.  This position has a heavily strategic component, responsible for the relationships with senior management of key partner and joint venture organizations pertaining to site operations. This position is also responsible for oversight of the Quality strategy for the assigned Biogen contract and/or internal program, including partner audit management and audit responses as well as the management of regulatory inspections related to partner programs or products.

　　This function has the responsibility to ensure the requirement of Global Quality System regulations are effectively established and maintained to provide PO&T with scalable Quality activities within the following business areas:

　　Disposition, release, and distribution of commercial and clinical drug substanceOversite of the engineering, facilities, maintenance, validation, QC, and manufacturing operations at the siteQuality Engineering support of site expansions, upgrades, and operationsOverall responsibility for site Change control, investigations, deviations, and site-related GxP documentationInspection readiness for all global regulatory markets (US, EU, Japan, BIR, MENA, etc.)  including inspections from partners and joint venture organizations.Oversees key interfaces and strategy for Biogen contracts and/or internal programs and guarantee the product release/distribution as current partnership agreements. What You'll Do

　　Quality oversight of Biogen manufacturing operations at the RTP BioManufacturing Site:

　　Develop and maintain strong and efficient relationships with internal partners (Manufacturing, Regulatory Affairs, Human Resources, Legal, Sourcing, and Finance) to ensure Global Quality goals and objectives are met. Lead, participate in, and provide direction to cross-functional teams related to product investigations, regulatory audits/inquiries, implementation of new/revised GxP guidelines, and PO&T strategic improvement initiativesInfluence and Negotiate Quality Agreements with corporate partners.Participate in BIIB Health Authority across multiple markets and manage RtQs associated with regulatory questions.Develop and maintain strong and efficient relationships with external partners to ensure adherence to Biogen standards, cGMP's and regulatory agency guidelinesEnsure performance is tracked and reported during Biogen management reviews. Develop and ensure execution and effectiveness verification of improvement action plans.Lead strategic initiatives to re-engineer business processes within Site Quality and within the PO&T organizationMake decisions regarding product disposition including release to market, regulatory reporting, and product disposition for all Biogen commercial and clinical products manufactured at the siteInfluence the development and execution of the Biogen External Supply Network Strategy and VisionDevelop and implement an onboarding quality strategy for partner / acquired clinical assets Ensure that the facilities, procedures, equipment, personnel, and process are continually evaluated and improved to ensure compliance.  Oversee the development, implementation, and maintenance of site Quality Systems that conform to Biogen Global Standards and Practices and cGMP:

　　Manage the QMS team for oversight of GxP activities with a focus on GMP manufacturing for commercial and clinical products. Ensure manufacture and distribution of Biogen products is performed in a safe, compliant manner, meeting the requirements defined by Biogen regulatory submissions, cGxP requirements, and Biogen Quality Agreements.Ensure that the Global Quality QMS is applied at all sites in accordance with the Global QMSEnsure that superuser support is maintained for critical business systems, including Oracle, Trackwise, PLM, and BIUSupport site and global management reviews as well as partner management reviews Lead and develop global teams:

　　Recruit, retain, and develop strong QA talent responsible for the management of quality operations to ensure the compliance of commercial and clinical products. Direct the Quality teams, including personal performance and development, in support of Corporate and Dept goals. Ensure team members are empowered, motivated, and have adequate development plans.Manage the utilization of Quality resources to ensure on-time supply of products and adherence to financial targets. Partner Relations:

　　Manage strategy of interactions with third-party senior management at leadership level to ensure optimal business operations for partner with concurrent security of the Biogen portfolio.Execute rights and responsibilities according to appointment as authorized signatory for Quality Agreement or other regulatory communications. Qualifications Required

　　Bachelor's of Science (B.S.) in Chemical Engineering, Biological Sciences or other relevant background required (PharmD, PhD or advanced degree strongly preferred)Minimum of 15 years of experience in the pharmaceutical industry, both on biological and solid forms products development and/or production.Minimum of 8 years of experience in Quality associated with biopharmaceutical / pharmaceutical production.Minimum of 5 years of experience managing people at Executive and mid-level managementMinimum of 5 years of experience in leading Global functions / Business UnitExtensive knowledge in GMPs, ICH and USA, EU, JP, ROW regulations and Contract ManufacturingStrong communication skillsStrong Influence and Negotiation skillsExtensive Business AcumenStrong ability to develop partnerships with others, both internally and externally. Focus on accuracy and staying compliant and understand the critical nature of working with customers and patients in mind. Continuous improvement mind-set as a core capability and drive strategic thinking, creativity, and operational excellence.  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.