Our client is a global pharmaceutical leader focused on advancing innovative therapies and ensuring patient access. They are seeking a Manager Regulatory Affairs to support and lead regional teams (Europe & Canada [EUCAN] or Growth & Emerging Markets [GEM]) in regulatory strategy and product life cycle management.
The selected candidate will be responsible for the following task area:
* Supporting the development and execution of regional regulatory strategies to ensure timely approval of investigations and marketing applications
* Collaborating with global and local teams to maintain compliance and optimise patient access
* Leading or assisting in submission working groups and representing the region in cross-functional teams
* Managing Health Authority communications and submissions in the assigned region
* Providing regulatory guidance throughout product development and life cycle phases
* Monitoring regulatory changes and adapting strategies accordingly
* Supporting internal process improvements and post-marketing commitments tracking
* Facilitating patient access initiatives and maintaining strong stakeholder relationships
* Preparing and leading Health Authority meetings and follow-ups
To be considered for this position, the ideal candidate must have:
Are you looking to add significant value in an international environment and play a key role in an exciting project? Then apply today!
Quote job ref
JN-082025-6809958
Job Function
Healthcare & Life Sciences
Specialisation
Pharmaceutical
Industry
Healthcare / Pharmaceutical
Location
Zürich
Contract Type
Interim
Job Reference
JN-082025-6809958
Job Nature
Home Office