Position Title:  Manager Medical Safety

Date:  Oct 7, 2026
Requisition ID:  34099
Work Location: 

Neuchatel, NE, CH, 2000

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At PMI, we’ve chosen to do something incredible. We’ve transformed our business and are building our future on one clear purpose—to deliver a smoke-free future.

With huge change comes huge opportunity. So, wherever you join us, you’ll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions.

We're looking for a Manager Medical Safety located in Neuchatel to provide robust safety expertise for assigned products through lifecycle management. 

Impact You'll Own

  • Be responsible for the product safety surveillance program
  • Oversee adverse events collection, evaluation, processing, assessment, reporting during and after clinical studies and post marketing safety surveillance.

What You'll Do

  • Ensure review/medical assessment of reported adverse events and serious adverse events. Apply standard pharmacovigilance procedures and guarantee compliance with requirements for adverse events’ assessment and regulatory reporting.
  • Support and review study protocol writing including all clinical study related documents; review of Safety Update Reports (SURs). Provide clinical information and safety reports as required by regulatory agencies/ethics committees (from clinical studies and consumer usage, spontaneous or solicited sources)
  • Oversee and assess safety trending/signal detection processes. Drive decision making on identified product risks. Participates in the resolution of legal liability, in compliance with internal standards/procedures as well as regulations - e.g. Good pharmacovigilance practices (GVP) and Good clinical practices (GCP)
  • Keep abreast of applicable rules/regulations. Create/deliver safety training to internal and external parties, within clinical evaluation projects.

Skills & Experience

  • Medical Doctor
  • Demonstrated experience in medical safety, safety signal detection and adverse event reporting
  • Good knowledge of ICH CGP, GVP, Regulatory Compliance, Pharmacovigilance and related standards
  • Strong proactive communication, flexibility/adaptability, within multi-functional teams.
  • Influence, Data Visualization, Data-Driven Storytelling, Category & Portfolio Knowledge, Pharmacovigilance Automation & AI Tools, Periodic Safety Update Reporting, Safety Data Systems.

What We Offer

Our success depends on the talented people who come to work every single day with a sense of purpose and an appetite for progress.

You will join a company that invests in you. We will support your growth as an employee through individual development and structured career management. You will join a dynamic, fast-paced work environment in a constantly evolving industry. Our employees have the courage, curiosity, and conviction to see possibilities where others only see challenges. We offer a competitive salary and benefits package. 

Application Process

  • Application review
  • Initial conversation with Talent Acquisition
  • Interview with Hiring Manager and Peers

Equal Opportunities Statement

We believe that diverse perspectives and experiences make us stronger. As an equal opportunity employer, we are committed to creating a workplace where every individual feels welcomed, respected, valued, and empowered to reach their full potential.

We encourage applications from people of all backgrounds and identities, and provide reasonable accommodations to ensure an accessible recruitment process. If you need support or adjustments during your application, let us know—we’re here to help you succeed.

The Talent Acquisition Team at PMI will be grateful for CVs/Resumes to be submitted in English.