Job Description

General Summary:

• Reporting to the Senior Director of Regulatory Affairs, the Country Associate Director (AD) of Regulatory Affairs will provide regional and local expertise as a member of the Global Regulatory Affairs (GRA) team to ensure Vertex establishes and implements best practices
• This individual will be responsible for providing local regulatory expertise to ensure Vertex establishes and implements best practices in accordance with national requirements in Switzerland

Key Duties and Responsibilities:

Regulatory

• Act as main contact with local National Health Authority (HA) Swissmedic for Regulatory Activities
• Track all HA requests and relevant new local legislation and diligently forward to relevant GRA contact
• Provide regional and local regulatory expertise, maintain current knowledge of local requirements and anticipate, assess and communicate changes to local and RA Senior Management in a timely manner
• Obtaining national regulatory intelligence through interaction with Swissmedic
• Act as local expert for regulatory queries coming from other functions, e.g. medical and supply chain, on topics such as compassionate use, exemption from local labelling, etc.
• Act as local contact for national requirements related to MAAs. Submission and follow-up of local MAAs and subsequent variations for nationally approved products in Switzerland
• Review and approval of translations for labelling, artwork and Product Information
• Review of promotional material according to the local requirements (AWV, Pharma Code)
• Participate in local cross-functional launch activities
• Ensure all work is compliant with regulatory requirements and company policies and procedures

General

• As applicable, support and contribute to local cross-functional and leadership teams to achieve corporate and departmental goals and objectives.
• Exhibit ownership and accountability for all projects and internal assignments; plan, schedule and arrange own work activities with limited direction
• Attend meetings at local or international Vertex Offices
• Exemplify Vertex’s core values in fulfilling these job duties

Knowledge and Skills:

Regulatory

• Extensive relevant industry experience in regulatory affairs and understanding of current trends in local and regional requirements; e xperience across the life-cycle (development and post-authorization).
• Specialized knowledge of local regulatory environments and stakeholders
• Recognized as a knowledgeable resource for regulatory advice by other departments
• Experience of managing complex negotiations with Regulatory Authorities
• Must be able to facilitate interactions with International Regulatory Affairs, other departments within the Company and external parties (national authorities, trade associations, professional bodies, etc.)
• Proactively identify risks and develop potential solutions

General

• Desire to be part of a highly innovative company aimed at transforming the lives of people with serious diseases, their families and society.
• Good interpersonal skills and ability to deal effectively with a variety of personalities
• Strategic ability, as evidenced by an awareness of the "big picture" strategic issues facing the business overall and positioning of local strategy relative to global and international requirements
• Self-motivated with the ability and desire to take on new challenges, to help build an organization and still be part of a team taking a hands-on approach to projects.
• Team player, but also able to behave independently where needed, at the same time this individual must understand and embrace being part of a team and working collaboratively with others.
• Strong analytical ability; and an ability to deal with ambiguity, uncertainty and complexity
• Display solid ethics and fully comply with all regulatory, legal and industry codes of conduct.
• Ability to navigate and be successful in a fast-paced environment while delivering high quality results.
• Accountability - e nsuring assigned projects are appropriately prioritised and progressed in accordance with agreed regulatory plans
• Excellent communication skills, strong oral/written presentation skills.
• Fluent written and spoken English

Education and Experience:

• Bachelor’s degree in life sciences required
• M.Sc. or Ph.D. degree is preferred.
• Experience in regulatory affairs with track record of success

#LI-SG1

#LI-Hybrid

Flex Designation:

Hybrid-Eligible Or On-Site Eligible

Flex Eligibility Status:

In this Hybrid-Eligible role, you can choose to be designated as:
1. Hybrid work remotely up to two days per week; or select
2. On-Site work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.

#LI-Hybrid

Company Information

Vertex 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 ApplicationAssistance@vrtx.com