Swissmedic Opens Medical Device Specialist Roles: Regulatory Careers in 2026

Swissmedic, the Swiss Agency for Therapeutic Products, has announced new job openings for 2026. These positions focus on medical device regulation, including market authorization, surveillance, and compliance. The roles are based in Bern and target professionals in regulatory affairs, clinical teams, and quality management within the medical device sector.

Swissmedic Career Opportunities

Swissmedic is actively recruiting specialists in medical devices to strengthen its regulatory team in 2026. The agency is seeking experts in areas such as:

  • Medical device market authorization
  • Post-market surveillance
  • Compliance and quality assurance

These positions are tailored for professionals with regulatory expertise, clinical experience, or quality management backgrounds, aiming to contribute to the oversight of therapeutic devices in Switzerland.

What Do These Roles Entail?

Market Authorization Roles

Market authorization specialists will evaluate medical devices for compliance with Swiss regulations before granting approval for market entry. This involves reviewing technical files, risk assessments, and conformity documentation.

Surveillance and Compliance

Professionals in surveillance roles will monitor devices already on the market to ensure ongoing compliance with safety and performance standards. This includes investigating adverse event reports and conducting audits.

Quality Management Experts

Quality managers will focus on establishing and maintaining robust systems to ensure that medical devices meet regulatory and quality requirements throughout their lifecycle.

How to Apply?

Interested candidates can find detailed job descriptions and application instructions on the Swissmedic Careers page. Applications should highlight relevant expertise in regulatory affairs, clinical operations, or quality management.

Frequently Asked Questions

  1. What qualifications are required for these roles?
    Swissmedic seeks candidates with experience in regulatory affairs, clinical operations, or quality management. Specific qualifications may vary by role.
  2. Where are these positions located?
    All positions are based in Bern, Switzerland.
  3. Is knowledge of Swiss medical device regulations essential?
    Yes, familiarity with Swiss regulations is highly desirable for these roles.

Conclusion

Swissmedic’s 2026 recruitment initiative offers exciting opportunities for professionals in medical devices. These roles are critical for ensuring the safety and compliance of therapeutic products in Switzerland. Interested candidates should act promptly to explore these career paths.

Disclaimer

This article is for informational purposes only and does not constitute legal or regulatory advice. Readers are encouraged to consult official sources or professional advisors for specific guidance.

Source

For full information, visit the original source at Swissmedic Careers.

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