Regulatory Affairs CMC Manager, contract jobYour new companyThis pharmaceutical company is looking for an experienced Regulatory Affairs CMC professional to join an established team on a contracting basis. This is a 12-month contract job with scope for extension, hybrid working is available, and there will be a need for an onsite presence in Cambridge.Your new roleAs Regulatory Affairs CMC Manager, you will be responsible for coordinating the preparation of high-quality CMC documents to support regulatory submissions in International regions (Asia, Latin America, Middle East, Eastern Europe and Africa).You will work with pharmaceutical development, manufacturing, QA and external partners to deliver the CMC components for marketing applications, variations and renewals as well as coordinating the preparation of responses to CMC questions from regulatory authorities.What you'll need to succeedIn order to be considered for this contract job as Regulatory Affairs Manager CMC, you must have significant Regulatory CMC experience and be capable of preparing and finalising CMC regulatory dossiers, as well as, managing the ongoing maintenance of existing product licenses.What you'll get in returnFlexible working options available.What you need to do nowFor more information on this or any other Regulatory Affairs contract jobs, please apply to this advert.
Back to search
Regulatory Affairs CMC Manager contract
Hays Specialist Recruitment Limited
Posted a day ago, valid for 23 days
Cambridge, Cambridgeshire CB2 8AG, England
£30,000 - £36,000 per annum
Full Time
In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.
Sonic Summary
- The job is for a Regulatory Affairs CMC Manager on a 12-month contract with potential for extension, requiring a hybrid working arrangement with some onsite presence in Cambridge.
- Candidates must have significant Regulatory CMC experience and be adept at preparing and finalizing CMC regulatory dossiers.
- The role involves coordinating the preparation of high-quality CMC documents for regulatory submissions in various international regions.
- The position offers flexible working options and the opportunity to work with pharmaceutical development, manufacturing, QA, and external partners.
- Salary details are not specified, but significant experience is required for consideration.