Lead Post Market Surveillance Specialist EMEA (m/f/x)

Work Flexibility: Hybrid

Why join Stryker? Looking for a place that values your unique talents? Discover Stryker's award-winning culture. Make a meaningful impact on patient safety and product quality across the EMEA region. In this role, you will help ensure medical devices remain safe, effective, and compliant throughout their lifecycle by supporting post-market surveillance activities and regulatory reporting processes. You will work across multiple countries and functions, partnering with regulatory, quality, commercial, and operational teams to drive compliance, continuous improvement, and business continuity. As this position is part of an international team, we kindly ask that you submit your CV in English.

What You Will Do

• Execute post-market surveillance activities in accordance with applicable regulations, quality requirements, and internal procedures.
• Coordinate product field actions and commercial hold activities across the EMEA region, ensuring impacted products and customers are accurately identified and managed.
• Manage regulatory notifications and submissions to competent authorities, including responses to requests for additional information.
• Monitor regulatory developments and post-market surveillance intelligence, maintaining accurate documentation and sharing relevant updates with stakeholders.
• Support country and regional teams to ensure operational continuity and consistent execution of post-market surveillance processes.
• Analyze performance data, prepare metrics and reports, and provide insights to support quality and regulatory objectives.
• Develop, update, and deliver training materials to support compliance, process adoption, and knowledge sharing across the organization.
• Contribute to process improvement initiatives, system implementations, and integration activities to enhance regional post-market surveillance effectiveness.

What You Will Need

• Bachelor's degree in Life Sciences, Engineering, Regulatory Affairs, Quality, or a related field.
• Minimum 4 years of experience in Regulatory Affairs, Quality Assurance, Post-Market Surveillance, or a related medical device environment.
• Knowledge of Medical Device Regulations, post-market surveillance requirements, and quality management systems.
• Experience supporting regulatory reporting, product field actions, complaints, or post-market surveillance processes.
• Fluency in English; additional languages will be considered a plus.
• Strong communication and interpersonal skills, with a positive, team-oriented mindset and the ability to remain effective under pressure while managing competing priorities.

Preferred Qualifications

• Regulatory Affairs Certification (RAC).
• Experience working across multiple countries or regions within the medical device industry.

Additional Information

Work arrangement: Hybrid working model based on business and country requirements.

Travel: Occasional regional travel may be required.

What we offer

• Flat hierarchies and responsibility.
• Through flat hierarchies, we strengthen the initiative and willingness of our employees to take over responsible tasks.
• We grow talent.
• At Stryker we offer great personal and internal career development for our employees, with the possibility to make both vertical and lateral position movement.
• Team spirit & engagement.
• We create engaged and inclusive teams that encourage colleagues to share their diverse perspectives and opinions.
• Competitive salary and Benefits.
• With us, you will receive a competitive salary and benefits commensurate with your job.
• Recognition of your performance.
• At our company, outstanding individual and cross-functional team performance is rewarded.
• Ideas, projects, or other exceptional achievements can be submitted for various awards on a local and global level.
• Employee Resource Groups (ERGs).
• Our ERGs are dedicated to fostering an inclusive, diverse, and supportive workplace environment.
• They provide opportunities for development, networking, and collaboration, and are open to all employees.
• Our ERGs are committed to promoting inclusion and belonging, helping every individual thrive and contribute to our shared success.

France Pay Ranges: France: €45.500 - €75.900 EUR Annual

Germany Pay Ranges: Berlin/Duisburg/Waghäusel/field-based 40Std: €69.400 - €115.700 EUR Annual

Spain Pay Ranges: Spain: €44.000 - €73.400 EUR Annual

Ireland Pay Ranges: Ireland: €54,000 - €90,000 EUR Annual

Romania Pay Ranges: Romania: lei12.300 - lei20.400 RON Monthly

Travel Percentage: 10%

Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better.

Stryker offers innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes.

We are proud to be named one of the World's Best Workplaces!

Work Flexibility Remote – Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location.

Field-based – You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based.

Onsite – Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category.

Hybrid – You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.