Executive Vice President Regulatory Affairs & Quality Management, Skåne

You will have the overall responsibility for the management and strategic direction of the global RA & QA function within the Med Tech company. The work will include leading the Regulatory Affairs and Quality Management team, ensuring that strategic and operational plans are inplace to deliver objectives.

Provide regulatory strategic input and support to the whole, organization, coordinate successful submissions, and approvals of all applications and also coordinate and manage external service providers and consultants are daily tasks. The position is both a strategic and operational position within the company. You will manage and have responsibility for the RA & QM functional budget and be part of the management team. 

The position is based at the company's headquarter in Southern Sweden.

If this is a position that appeals to you and you believe you have the required experience, skills, and knowledge plus commitment I would very much discuss further with you.

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