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Senior Staff Regulatory Affairs (m/f/d)

Stryker

Senior Staff Regulatory Affairs (m/f/d)

full-timePosted: Aug 11, 2026Updated: Aug 28, 2026Switzerland, Selzach

Job Description

Work Flexibility: Hybrid or OnsiteAs 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:Lead regulatory strategy for new products and changes, ensuring global compliancePrepare and manage submissions (e.g., FDA, EU MDR, post-market reports)Act as a liaison with regulatory authorities and notified bodiesReview and approve labeling, marketing, and change documentationSupport audits and inspections, providing expert regulatory guidanceMonitor regulatory trends and communicate updates internallyMentor junior RA team members and support training activitiesContribute to process improvements and SOP developmentWhat will you need:Required:Bachelor’s degree in life sciences, engineering, or related field5+ years of experience in medical device Regulatory AffairsStrong knowledge of FDA, EU MDR, and global regulationsProven experience with Class II/III medical device submissionsExcellent English communication skillsPreferred:Master’s degree or Regulatory Affairs Certification (RAC)Experience in orthopedics or implantable devicesGerman language skillsFamiliarity with Quality Systems and Design ControlDiversity is important to us. 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. 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%

Locations

  • Switzerland, Selzach

Skills Required

  • medical device Regulatory Affairsintermediate
  • FDAintermediate
  • Class II/III medical device submissionsintermediate
  • orthopedicsintermediate
  • Quality Systemsintermediate

Required Qualifications

  • Bachelor’s degree in life sciences, engineering, or related field (degree in life sciences)
  • 5+ years of experience in medical device Regulatory Affairs (experience, 5 years)
  • Strong knowledge of FDA, EU MDR, and global regulations (experience)
  • Proven experience with Class II/III medical device submissions (experience)
  • Excellent English communication skills (experience)
  • Bachelor’s degree in life sciences, engineering, or related field (degree in life sciences)
  • 5+ years of experience in medical device Regulatory Affairs (experience, 5 years)
  • Strong knowledge of FDA, EU MDR, and global regulations (experience)
  • Proven experience with Class II/III medical device submissions (experience)
  • Excellent English communication skills (experience)

Preferred Qualifications

  • Master’s degree or Regulatory Affairs Certification (RAC) (degree in regulatory affairs certification)
  • Experience in orthopedics or implantable devices (experience)
  • German language skills (experience)
  • Familiarity with Quality Systems and Design Control (experience)
  • Master’s degree or Regulatory Affairs Certification (RAC) (degree in regulatory affairs certification)
  • Experience in orthopedics or implantable devices (experience)
  • German language skills (experience)
  • Familiarity with Quality Systems and Design Control (experience)

Benefits

  • general: Switzerland: CHF108,500 - CHF181,000 CHF Annual
  • general: 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.
  • general: 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.

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