Descrição da Função

Your new company
Join a leading pharmaceutical company assuming a Quality Product Manager position, based in Lisbon.

Your new role
This professional will be responsible for planning, defining, compiling, revising, and maintaining the quality section of the dossier for the Lifecycle product portfolio worldwide. This professional will proactively develop global regulatory CMC strategies for active substances and finished products in cooperation with Production, Quality Control, Regulatory Affairs, and other Quality Assurance functions. Additionally, this professional will identify and mitigate potential regulatory risks or roadblocks, develop mitigation plans as needed, ensure regulatory compliance of the supervised product portfolio.

What you'll need to succeed
We are looking for a professional with a degree as a Pharmacist, with experience in Lifecycle Regulatory CMC for NCEs. Knowledge of medical devices is beneficial. This professional should have a proven track record in QA and/or GMP environments, especially for Change Management, and in-depth knowledge of relevant national and international guidelines and regulatory requirements for regions such as the US, EU, and Japan. Strong decision-making skills, even in challenging situations, and excellent oral and written communication skills in English are essential. 

What you'll get in return
This is an excellent opportunity to join a leading pharmaceutical company, with attractive benefits and a good work environment.

What you need to know
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.

Contacto

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