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 Track Wise

Salary information will be provided during the recruitment process.

Travel Percentage: 0%