Regulatory CMC Associate Director job in Cambridge, England

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First Name*

Last Name*

Email*

Phone Number*

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Are you an employer or a jobseeker?*

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First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

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Job type: Permanent

Discipline: Good Manufacturing Practice (GMP)

Location: United Kingdom

This vacancy has now expired. Please see similar roles below...

Proclinical are in partnership with a pharmaceutical company in search for a Regulatory CMC Associate Director. You will provide product support to the Chemistry, Manufacturing and Controls (CMC) function, which is responsible for Module 3 of regulatory submissions across phases of product development from clinical to lifecycle. Support may include organising, managing and executing on regulatory CMC projects and submissions.

Skills and Requirements

Degree in life sciences, biochemistry, or chemistry
Must have a proven track record within Biologics (5 years+).
Proficient skills in Microsoft Office suite, especially Word, Excel, PowerPoint and Project;
Ability to work both independently and as a member of a team.
Hiring Manager is also looking for someone with experience of working on global projects.

To Apply

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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