Senior Regulatory Affairs Specialist 100% CDI

Medtronic Europe Sàrl; Tolochenaz; On-site; CHF 120,000 - 160,000; Full time

Job summary

Medtronic Europe Sàrl in Tolochenaz (VD) seeks a Senior Regulatory Affairs Specialist for a 100% permanent role. You will coordinate regulatory submissions, renewals, and inspections, and advise on labeling, manufacturing, and clinical protocol changes to ensure compliance.

Immediate start and strong cross‑functional collaboration required. The role emphasizes tracking systems, regulatory strategy, and interactions with authorities, with a focus on timely approvals and maintaining high quality

Qualifications

• Bachelor's degree in a relevant field.
• More than 3 years regulatory affairs experience.
• Fluent in French, Swiss German, Italian, and English.

Responsibilities

• Directs or coordinates regulatory submissions from all areas.
• Leads license renewals and annual registrations.
• Recommends changes for labeling, manufacturing and clinical protocols for compliance.
• Direct interaction with regulatory agencies as needed.

Skills

Regulatory affairs

Documentation coordination

Clinical trial submissions

Regulatory inspections

Education

Bachelor’s degree or equivalent

Job description

Senior Regulatory Affairs Specialist 100% CDI

Medtronic Europe Sàrl Vacant since : 22.09.2026 Number of jobs : 1 1131 Tolochenaz (VD) 100% Immediately Permanent

Responsibilities may include the following and other duties may be assigned.

• Directs or performs coordination and preparation of document packages for regulatory submissions from all areas of company, internal audits and inspections. Leads or compiles all materials required in submissions, license renewal and annual registrations. Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance. Monitors and improves tracking / control systems. Keeps abreast of regulatory procedures and changes. May direct interaction with regulatory agencies on defined matters. Recommends strategies for earliest possible approvals of clinical trials applications.

• Work location 1131 Tolochenaz (VD)
• Workload 100%
• Employment start Immediately
• Employment duration Permanent

• Qualification skilled
• Work experience More than 3 years
• Education Bachelor’s degree from a university or equivalent

• French Orally : Very good knowledge Written : Very good knowledge
• Swiss German Orally : Very good knowledge Written : Very good knowledge
• Italian Orally : Very good knowledge Written : Very good knowledge
• English Orally : Very good knowledge Written : Very good knowledge

• By email [e-mail]