Senior Regulatory Affairs Specialist (fixed-term contract until October 2027)
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Job Location:
Monthly Salary:
Posted on:
5 days ago
Vacancies:
1 Vacancy
Job Summary
Work Flexibility: Hybrid
What You Will Do:
- 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
What You Need:
Required:
- 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
Preferred:
- Experience with NC/CAPA management
- Experience with TrackWise
Salary information will be provided during therecruitment process.
Travel Percentage: 0%Required Experience:
Senior IC
About Company
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. Alongsid ... View more
