Senior Regulatory Affairs Specialist (fixed-term Contract Until October 2027)
Stryker
Polska
Hybrid
2 years medical device industry experience
Knowledge of medical device quality management systems
English and polish full professional proficiency
The role involves supporting product notification and market access activities for Stryker Polska while maintaining data accuracy in regulatory databases
Job Summary
The role involves supporting product notification and market access activities for Stryker Polska while maintaining data accuracy in regulatory databases.
Candidates will act as a primary regulatory partner to local Sales, Marketing, and Tenders teams, providing training and guidance on regulatory changes.
The position requires monitoring evolving medical device regulations and supporting post-market activities related to product complaints and field actions.
Matching Summary
The role involves supporting product notification and market access activities for Stryker Polska while maintaining data accuracy in regulatory databases.
Skills & Requirements
Must-have
2 years medical device industry experience
Knowledge of medical device quality management systems
English and Polish full professional proficiency
Nice-to-have
Experience with NC/CAPA management
Experience with TrackWise software
Action-oriented results-driven mindset
Key Requirements
2 years experience in medical device industry
Full professional proficiency in English and Polish