Regulatory Affairs Lead - Generics, Post-Approval Expert

Regulatory Affairs Lead - Generics, Post-Approval Expert

Full-Time No working from home possible
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Select Pharma Recruitment is seeking an experienced Regulatory Affairs Manager for a growing generic pharmaceutical company in the UK, supporting a portfolio of 220 licenses and ensuring robust compliance across product lifecycle.

You will take ownership of post-approval activities, oversee variations, labeling changes, renewals, and communications with MHRA and other authorities, and work with manufacturing, PV and QA teams to drive timely, compliant submissions.

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Regulatory Affairs Lead - Generics, Post-Approval Expert employer: Select Pharma Recruitment

Join a dynamic and innovative pharmaceutical company that values compliance and integrity, offering a supportive work culture where your expertise in Regulatory Affairs will be recognised and rewarded. With a strong focus on employee development, you will have access to continuous training and growth opportunities, all while working in a collaborative environment that prioritises teamwork and open communication. Located in a thriving area, this role not only provides a chance to make a significant impact but also offers a fulfilling career path in a sector dedicated to improving health outcomes.

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Contact Details:

Select Pharma Recruitment Recruitment Team