25.02.2025 | Pełny etat | Warszawa | Randstad Polska Sp. z o.o.Regulatory Affairs Manager who will manage the operational delivery of regulatory documents for product registration and compliance. This person will manage the team and coordinate the plans for packages of documents sent. If you have relevant experience and you are ready for new professional
Zobacz później24.02.2025 | Pełny etat | Warszawa | Randstad Polska Sp. z o.o.We are seeking a highly skilled Regulatory CMC Manager to play a vital role in shaping global regulatory strategies for innovative pharmaceutical products. In this position, you will lead the preparation of regulatory dossiers, collaborate with cross-functional teams, and provide expert guidance
Zobacz później24.02.2025 | Pełny etat | Warszawa | Randstad Polska Sp. z o.o.Step into a pivotal role as Manager, Regulatory Affairs and contribute to the global development and lifecycle management of groundbreaking pharmaceutical products. As a key member of team, you will lead the development and execution of global CMC regulatory strategies, ensure compliance
Zobacz później24.02.2025 | Pełny etat | Warszawa | Randstad Polska Sp. z o.o.For our Client, one of the largest Pharmaceutical companies worldwide, we are looking for Regulatory Affairs Mananger - Senior Manager in Global Labeling, who will ensure quality of primary and derived labeling documents and ensure support for the documents. If you have relavant experience
Zobacz później01.01.2012 | Pełny etat | Mazowieckie | Hays PolandOf the company range of products in Poland in mid-2011 Important Responsibilities - Regulatory project management in Central European Countries (with focus on Poland) from concept to market delivery and support. To actively work with European Product Safety and Regulatory Affairs organisation (based in London
Zobacz później01.01.2012 | Pełny etat | | Stany Zjednoczone | PSI PolskaForeign Regulatory Affairs Manager will be responsible for coordination and management of all aspects associated with the registration of products in EU, Asia and South America (OTC & Rx). In cooperation with local management and regional regulatory he/she will define registration strategy
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