Vertex Switzerland Distribution Posted June 24, 2026

Regulatory Strategy Associate Director

Zug, Switzerland Full time
Regulatory Affairs Associate Director

Vertex Switzerland Distribution is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Description

General Summary:

Reporting to the Senior Director of Regulatory Affairs and partnering closely with the cross-functional leadership team and the Swiss Country Manager, the Country Associate Director (AD) of Regulatory Affairs will act as a local strategic leader and key partner within the International Regulatory Affairs team. This role is critical in shaping and executing the regulatory strategy for Switzerland, ensuring alignment with global objectives while addressing local regulatory requirements.

The AD will demonstrate leadership, accountability, and collaboration to drive impactful outcomes for Vertex and its stakeholders.

Key Duties And Responsibilities

Regulatory

Inform the development and execution of innovative regulatory strategies to support product launches, lifecycle management, and compliance initiatives.

Translate the global regulatory strategy into actionable plans tailored to the Swiss regulatory environment, ensuring alignment with corporate goals.

Act as a strategic advisor to local senior leadership, providing insights and recommendations to anticipate and address regulatory trends.

Shape regulatory direction by influencing internal and external stakeholders, ensuring Vertex is positioned for success in the Swiss market.

Serve as the primary liaison with Swissmedic, leading all regulatory interactions, negotiations, and meetings with a focus on building trusted relationships.

Take full ownership of regulatory planning and execution for local Marketing Authorization Applications (MAAs), lifecycle management submissions, and compliance with national requirements.

Ensure timely and accurate communication of regulatory intelligence, legislative changes, and health authority requests to internal stakeholders.

Oversee the review and approval of promotional, medical, and educational materials, ensuring compliance with local regulations.

General

Actively engage with local cross-functional teams, including Commercial, Medical Affairs, Market Access, Quality, and Supply Chain, to align regulatory priorities with business objectives.

Represent Regulatory Affairs in local cross-functional forums, driving alignment and shared accountability across teams.

Build and maintain strong partnerships with external consultants, industry stakeholders, and trade associations to advance regulatory objectives

Contribute to cross-functional launch activities, ensuring regulatory readiness and operational excellence.

Knowledge And Skills

Regulatory

Extensive experience in regulatory affairs, with a proven track record of strategic leadership and successful regulatory negotiations.

In-depth knowledge of the Swiss regulatory environment, including requirements for innovative products across development and post-authorization phases.

Ability to influence internal and external stakeholders, with strong communication and presentation skills.

Demonstrated capacity to navigate complex, fast-paced environments with resilience, adaptability, and a focus on delivering high-quality results.

Commitment to fostering a collaborative and inclusive work environment, aligned with Vertex’s core values.

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 - ensuring assigned projects are appropriately prioritised and progressed in accordance with agreed regulatory plans

Education And Experience

Bachelor’s degree in life sciences required; advanced degree ( M.Sc . or Ph.D.) preferred.

Significant experience in regulatory affairs, with a focus on strategic leadership and cross-functional collaboration.

Fluency in written and spoken English; proficiency in German is highly desirable.

Flex Designation

Hybrid-Eligible Or On-Site Eligible

Flex Eligibility Status

In this Hybrid-Eligible role, you can choose to be designated as:

Hybrid: work remotely up to two days per week; or select

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-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

Job details

Seniority
Associate Director
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Zug, Switzerland
Employment type
Full time

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 171 comparable Associate Director Regulatory Affairs roles across 50 biopharma companies.

171Comparable roles tracked
165Currently active
50Companies hiring similar roles
28Countries represented

Salary context

49 of 171 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Chemistry Manufacturing Controls Manager · Vertex Pharmaceuticals Inc (US) $0/hr – $0/hr (≈ $0–$0/yr)
Highest disclosed · Regulatory Strategy Associate Director · Vertex Pharmaceuticals Inc (US) $168,000/yr – $252,000/yr
Peer group range $0 – $210,000 (median $180,500)

Where these roles are based

Top locations among the 171 comparable roles

United States70
India18
Ireland11
Japan11
Poland10
China8

+ 22 more countries

Seniority mix

171 of 171 peers have a known seniority level

Manager115
Associate Director30
Senior26

Therapeutic area mix

23 of 171 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology8
Dermatology & Aesthetics6
Neuroscience5
Immunology4

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

50%similar
AbbVie Cham, ZG Manager
Same function Adjacent seniority Same country
45%similar
Lilly Ontario, Ontario, Canada Associate Director
Same function Same seniority
45%similar
Lilly Shanghai, Shanghai, China Associate Director
Same function Same seniority
45%similar
Lilly Cork, Cork, Ireland Associate Director
Same function Same seniority
45%similar
AbbVie Mettawa, IL Associate Director
Same function Same seniority
45%similar
AbbVie Mettawa, IL Associate Director
Same function Same seniority

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

50%
Regulatory Affairs Manager (80%)
AbbVie · Cham, ZG · Manager
Function Therapeutic area Adjacent seniority Country
45%
Associate Director/ Director - Global Regulatory Scientist
Lilly · Cork, Cork, Ireland · Associate Director
Function Therapeutic area Seniority Country
45%
Associate Director, International Regulatory Affairs Advertising & Promotion
AbbVie · Mettawa, IL · Associate Director
Function Therapeutic area Seniority Country
45%
Associate Director, Regulatory Affairs US & Canada Strategy Lead – Facial Aesthetics - Device
AbbVie · North Chicago, IL · Associate Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.