Senior Staff Regulatory Affairs (m/f/d) — Stryker
- Location
- Selzach
- Contract
- full-time
- Posted
- Yesterday
Role overview
Work Flexibility: Hybrid or Onsite
As a Senior Staff Regulatory Affairs Specialist (m/f/d) at Stryker, you will lead global regulatory strategies for innovative medical devices.
Reporting to the Regulatory Affairs Manager, you'll support cross-functional teams, mentor colleagues, and ensure compliance across international markets, including the US and EU. What will you do:
- Work Flexibility: Hybrid or Onsite
- As a Senior Staff Regulatory Affairs Specialist (m/f/d) at Stryker, you will lead global regulatory strategies for innovative medical devices.
Application process
- We welcome applications from people regardless of their ethnic, national or social origin, gender, disability, age or sexual identity. Additional information
- Thanks to our flexible working hours model, you will have the opportunity to work partially from the home office.
- However, a regular presence on site at our location in Kiel should be always given to build sustainable relationships and maintain personal contact with colleagues as well as the departments.
- Please note that the internal job title may differ from the ad title. Switzerland Pay Ranges: Switzerland : CHF108,500 CHF181,000 CHF Annual
- At Stryker, we believe transparency helps candidates make confident decisions about their next career step.
- Compensation is an important part of that process and we want to be clear about how pay is determined.
- The compensation information posted for this role may be presented as a salary range or a fixed amount depending on the role.
- In addition to base salary, this role may be eligible for incentive compensation (such as bonus and/or commissions where applicable), along with Stryker’s comprehensive benefits package.
Additional details
- Reporting to the Regulatory Affairs Manager, you'll support cross-functional teams, mentor colleagues, and ensure compliance across international markets, including the US and EU.
- Contribute to process improvements and SOP development What will you need:
- Proven experience with Class II/III medical device submissions Excellent English communication skills
- Experience in orthopedics or implantable devices German language skills
- We welcome applications from people regardless of their ethnic, national or social origin, gender, disability, age or sexual identity. Additional information
- Please note that the internal job title may differ from the ad title. Switzerland Pay Ranges: Switzerland : CHF108,500 CHF181,000 CHF Annual
- If you’d like to learn more about the salary or the benefits associated with this role, your recruiter will be happy to walk you through the details as you progress through the hiring process. Travel Percentage: 10%
Notes and original content
- What will you do:
- Contribute to process improvements and SOP development
- What will you need:
- Proven experience with Class II/III medical device submissions
- Excellent English communication skills
- Experience in orthopedics or implantable devices
- German language skills
- We welcome applications from people regardless of their ethnic, national or social origin, gender, disability, age or sexual identity.
- Additional information
- Please note that the internal job title may differ from the ad title.
Questions about this listing
What salary does Stryker offer for this role?
Stryker lists CHF 94'500 - 143'000 gross per year for this position in Selzach. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Stryker offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Stryker during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Solothurn?
EU/EFTA residents living in the border zone of the country adjoining Canton Solothurn can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Solothurn's cantonal migration office or with HR during the application.
How do I apply for this position at Stryker?
Use the "Apply now" button on this page — it links directly to Stryker's original listing at stryker.wd1.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
