Senior Staff Regulatory Affairs (m/f/d)

Return to Search
Apply Now
  • Schönkirchen, SH, 24232, DE
  • Remote-DE
Job details
Work flexibility: Remote Req ID: R561312 Employee type:
  • Temporary
  • Full Time
Job category: RAQA Travel: 10% Relocation: No

Related content

Why join Stryker?

Looking for a place that values your unique talents? Discover Stryker's award-winning culture.

We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.

Job description

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.

This position is limited to 30 June 2027.

What will you do:

  • Lead regulatory strategy for new products and changes, ensuring global compliance

  • Prepare and manage submissions (e.g., FDA, EU MDR, post-market reports)

  • Act as a liaison with regulatory authorities and notified bodies

  • Review and approve labeling, marketing, and change documentation

  • Support audits and inspections, providing expert regulatory guidance

  • Monitor regulatory trends and communicate updates internally

  • Mentor junior RA team members and support training activities

  • Contribute to process improvements and SOP development

What will you need:

Required:

  • Bachelor’s degree in life sciences, engineering, or related field

  • 5+ years of experience in medical device Regulatory Affairs

  • Strong knowledge of FDA, EU MDR, and global regulations

  • Proven experience with Class II/III medical device submissions

  • Excellent English communication skills

Preferred:

  • Master’s degree or Regulatory Affairs Certification (RAC)

  • Experience in orthopedics or implantable devices

  • German language skills

  • Familiarity with Quality Systems and Design Control

Diversity 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. 

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology and Orthopaedics that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.

Apply Now
Globe Icon An icon representing a globe