Director, Regulatory CMC, Biologics (Boston)

Job DescriptionGeneral Summary:The Director, Chemistry Manufacturing Controls leads a team in the execution of multi-product global regulatory CMC strategies for investigational and marketed products. This role is accountable for the preparation and filing of regulatory CMC submissions and managing the interactions with Health Authorities for CMC topics. This role provides regulatory guidance to various cross-functional teams to ensure all applicable global regulatory requirements are considered and appropriately incorporated into investigational and marketed products. This role will lead a group within Regulatory CMC responsible for multiple programs/products.Key Duties and Responsibilities:Oversees the preparation and review of CMC sections of regulatory submissions, and leads the interactions and responses with regulatory agenciesLeads the development of global CMC regulatory strategies for multiple investigational and/or marketed productsLeads the design, development and implementation of department strategies and contributes to the strategic planning for the areaEnsures assigned projects are appropriately resourced and is accountable for the results of the teamAs a people manager within the organization, may have financial accountabilities and human resource responsibilities for assigned staff.Knowledge and Skills:Excellent interpersonal skills to influence others internally and/or externally and to negotiate with others in a limited capacityAdvanced strategic thinking and problem solving skillsCollaborates and communicates in an open, clear, complete, timely, and consistent mannerStrong sense of planning and prioritization, and the ability to work with all levels of managementComprehensive knowledge of regulatory (FDA, EMA, Health Canada and ICH) guidelinesExperience with development and/or improvement of department processes/proceduresProven ability to impact and influence the decisions of a team and decision making committeesStrong experience managing technical individualsEducation and Experience:Bachelor's, Master's or PhD degree in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices, or another life-science fieldTypically requires 10 years of experience in the pharmaceutical or biotech industry or in a related field and 3 years of supervisory/management experience, or the equivalent combination of education and experienceFlex Designation:Hybrid-Eligible Or On-Site EligibleFlex Eligibility Status:In this Hybrid-Eligible role, you can choose to be designated as:Hybrid : work remotely up to two days per week;On-Site : work five days per week on-site with ad hoc flexibility.Company InformationVertex is a global biotechnology company that invests in scientific innovation. Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at

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