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Production Compliance Coordinator

CV-Library

Posted on Jun 24, 2026 by CV-Library
Hatfield, Hertfordshire, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
Talentmark are recruiting for an Production Compliance Coordinator, to join a long-established global pharmaceutical company, based in Hatfield, on a permanent basis.

The Company:
Our client are a UK pharmaceutical company focused on researching and developing innovative, effective therapies for neurodegenerative diseases, such as Alzheimer's and Parkinson's.

Your main duties will be:

Coordinate production compliance activities to ensure GMP standards are maintained.
Prepare and maintain batch records and controlled documentation.
Support SOP, training record, and risk assessment development.
Track CAPAs, action items, and investigation outcomes.
Assist with quality investigations and compliance reviews.
Collaborate with Quality, Technical, and Production teams.
Identify and support continuous improvement opportunities.
Your Background:

Good understanding of GMP principles and regulated manufacturing environments (desirable).
Strong attention to detail and documentation accuracy.
Experience working with regulated processes and procedures.
Effective written and verbal communication skills.
Strong organisation, planning, and prioritisation abilities.
Apply:

It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence.

If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (Talentmark) and follow us to see our latest jobs and company news

Reference: 225289419

https://jobs.careeraddict.com/post/113458852
CV-Library

Production Compliance Coordinator

CV-Library

Posted on Jun 24, 2026 by CV-Library

Print
Hatfield, Hertfordshire, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
Talentmark are recruiting for an Production Compliance Coordinator, to join a long-established global pharmaceutical company, based in Hatfield, on a permanent basis.

The Company:
Our client are a UK pharmaceutical company focused on researching and developing innovative, effective therapies for neurodegenerative diseases, such as Alzheimer's and Parkinson's.

Your main duties will be:

Coordinate production compliance activities to ensure GMP standards are maintained.
Prepare and maintain batch records and controlled documentation.
Support SOP, training record, and risk assessment development.
Track CAPAs, action items, and investigation outcomes.
Assist with quality investigations and compliance reviews.
Collaborate with Quality, Technical, and Production teams.
Identify and support continuous improvement opportunities.
Your Background:

Good understanding of GMP principles and regulated manufacturing environments (desirable).
Strong attention to detail and documentation accuracy.
Experience working with regulated processes and procedures.
Effective written and verbal communication skills.
Strong organisation, planning, and prioritisation abilities.
Apply:

It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence.

If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (Talentmark) and follow us to see our latest jobs and company news
Print

Reference: 225289419

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