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CMC Regulatory Affairs Manager

Park Street People
Posted 2 days ago, valid for 20 days
Location

Uxbridge, Buckinghamshire UB8 1DH, England

Contract type

Part 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

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  • Our client, a global pharmaceutical company, is seeking a CMC Regulatory Affairs Manager for a temporary contract in Uxbridge.
  • The role involves executing CMC regulatory strategies, overseeing regulatory submissions, and liaising with various stakeholders.
  • Candidates should have previous experience in global and international Regulatory Affairs, particularly within the pharmaceutical industry.
  • Experience with the full regulatory lifecycle and knowledge of biologics and biosimilars is highly advantageous.
  • The position offers a salary of £65,000 per year and requires a minimum of 5 years of relevant experience.

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 legislation

Requirements

  • 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 manner

Park 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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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.