Senior Regulatory Affairs Specialist (fixed-term contract until October 2027)

Job description

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 Required: Preferred: Salary information will be provided during the recruitment process. Travel Percentage: 0% - 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 mi...