Reference Number: JO-2010-456015
Regulatory Affairs, CMC Manager
Rate: Negotiable
Job Type: Permanent
Location: Cambridge

Role: Regulatory Affairs, CMC Manager
Location: Cambridge
Salary: Highly competitive + benefits
employment: full time, permanent

Regulatory Professionals are collaborating with a biopharmaceutical company that researches, develops, and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV, hepatitis B, hepatitis C, and influenza, including Harvoni and Sovaldi. Our client is looking for an experienced CMC Manager who will provide CMC regulatory support for their investigational and commercial products across Europe, with a focus on supporting products in HIV, Inflammatory Diseases, and Emerging Viral Diseases therapy areas.

Other duties will include:

Preparation and/or coordination of regulatory submissions for our clients investigational and commercial products in the EU and International markets, primarily supporting the HIV, Inflammatory Diseases, and Emerging Viral Diseases programs. This could include the support of major MAA submission filings in the EU, Switzerland, and Israel.
Preparation of high-quality chemistry, manufacturing, and controls (CMC) documentation to support original MAAs, variations, and renewals.
Preparation of Quality components for investigational medicinal products to support clinical trial applications and amendments in the EU and International markets.
Co-ordination of responses to CMC questions from regulatory authorities.
Offering input on CMC regulatory requirements to manufacturing and pharmaceutical development groups for clinical trials, new product registrations, and post-approval changes.
Providing regulatory assessments for proposed changes to investigational and commercial products.
Sustaining an up-to-date awareness of CMC regulatory requirements for applicable territories and communicating key intelligence to the organization in a timely manner.
Originating or contributing to local process improvements that have an impact on the working of the Regulatory Affairs function or other departments.

Knowledge, Experience & Skills


Right to work in the UK
Typically requires a BA or BS degree in a relevant discipline and relevant experience in CMC Regulatory Affairs.
Experience in the preparation and maintenance of CMC components for regulatory submissions.
General understanding of CMC regulatory requirements and quality guidelines, including ICH and regional requirements.
Excellent organization skills and ability to work on several simultaneous projects with tight timelines.
Excellent verbal and written communication skills and interpersonal skills.


Regulatory Affairs CMC experience of investigational and commercial products.
Relevant industry experience is advantageous.

If you would like to apply for this position, please contact Amani via amani@regulatoryprofessionals.com. If you are not currently looking but know someone who would be good for this role then get in touch. We offer a referral scheme at Regulatory Professionals where in which a successful recommendation will earn you 250 worth of vouchers *terms and conditions apply*

Upload your CV and any other relevant file.
I would like to be contacted via SMS
I have read and agree to the Clinical Professionals Group Privacy Policy

Find our privacy policy here