Job details
What You Will Do:
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, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. - Support product notification and market access activities for Stryker Polska
- Maintain accuracy of data in Stryker regulatory databases and in the local ERP system
- Provide regulatory documentation to tenders, distributors and customers
- Communicate regulatory changes, assess commercial impact of changes and discontinuations
- Act as a primary regulatory partner to local Sales, Marketing, Tenders, provide training and regulatory guidance
- Act as a primary regulatory partner to regional and divisional regulatory teams
- Monitor evolving medical device and environmental regulations
- Support post-market activities related to product complaints, holds and field actions
- Support maintenance and audit readiness of local QMS
- 2 years of experience in the medical device industry
- Knowledge of medical device quality management systems and regulatory compliance
- English and Polish full professional proficiency
- Communication and collaboration skills to foster connections with other teams.
- Action-oriented with results-driven mindset
- Attention to detail
- Experience with NC/CAPA management
- Experience with TrackWise
Salary information will be provided during the recruitment process.
Required Skills
Senior Regulatory Affairs Specialist (fixed-term contract until October 2027)
Onsite Warsaw, Poland Junior Posted a day ago