CMC Regulatory Affairs Manager

Uxbridge
9 months ago
Applications closed

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Senior Project Manager, R&D: Drug Development

Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract.

This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their science.

Key Responsibilities

A key role in the execution of CMC regulatory strategies working on multiple cross functional projects
Oversee all regulatory submissions as well as reviewing and altering dossiers as necessary ensuring that these are compliant
Liaise with and build good relationships with affiliates, sites, regulatory agencies and other internal and external stakeholders
Maintain an active awareness of global Regulatory legislationRequirements

Previous experience in global and international Regulatory Affairs and Compliance particularly within the pharmaceutical industry
Full regulatory lifecycle process experience highly advantageous
Good understanding of regulatory procedures such as technical transfers, supply critical renewals
Biologics and biosimilars experience
Strong communication and stakeholder engagement skills
Proactive mannerPark Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Business in relation to this role

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