Quality Assurance Administrator
Posted on Jul 1, 2026 by CV-Library
Saltley, West Midlands (County), United Kingdom
Pharmaceutical
Immediate Start
£27k - £29k Annual
Full-Time
Talentmark are recruiting for an QA Administrator, to join a pharmaceutical company, based in Birmingham, on a permanent basis.
The salary is around £27,000-£29,000 per annum.
The Company:
Our client are a Pharma manufacturing company who produce, import, and distribute bespoke medicines (Specials), and CBPMs (Cannabis-Based Products for Medicinal Use).
Your main duties will be:
Manage the lifecycle of all controlled documents within the paper-based QMS (SOPs, forms, master documents, batch records, policies and specifications).
Provide administrative support for deviations, NCs, CAPAs, change controls, complaints and incident reports.
Ensure document activities comply with EU GMP (as applicable to Specials), MHRA expectations, and internal quality procedures.
Work closely with Production, QC and QA teams to ensure correct and timely use of controlled documents.
Design and execute method validation/verification, method transfers and robustness studies as required.
Your Background (Essential):
Degree in scientific, pharmaceutical or quality-related discipline.
Previous administration experience in an office or documentation-focused role.
Strong command in Microsoft Excel.
Your Background (Desireable):
Familiarity with core GMP documentation.
Experience in a GMP, pharmaceutical, specials or other regulated environment.
Knowledge of Specials Manufacturing regulatory requirements and MHRA guidance.
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
The salary is around £27,000-£29,000 per annum.
The Company:
Our client are a Pharma manufacturing company who produce, import, and distribute bespoke medicines (Specials), and CBPMs (Cannabis-Based Products for Medicinal Use).
Your main duties will be:
Manage the lifecycle of all controlled documents within the paper-based QMS (SOPs, forms, master documents, batch records, policies and specifications).
Provide administrative support for deviations, NCs, CAPAs, change controls, complaints and incident reports.
Ensure document activities comply with EU GMP (as applicable to Specials), MHRA expectations, and internal quality procedures.
Work closely with Production, QC and QA teams to ensure correct and timely use of controlled documents.
Design and execute method validation/verification, method transfers and robustness studies as required.
Your Background (Essential):
Degree in scientific, pharmaceutical or quality-related discipline.
Previous administration experience in an office or documentation-focused role.
Strong command in Microsoft Excel.
Your Background (Desireable):
Familiarity with core GMP documentation.
Experience in a GMP, pharmaceutical, specials or other regulated environment.
Knowledge of Specials Manufacturing regulatory requirements and MHRA guidance.
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: 225318340
https://jobs.careeraddict.com/post/113497131
Quality Assurance Administrator
Posted on Jul 1, 2026 by CV-Library
Saltley, West Midlands (County), United Kingdom
Pharmaceutical
Immediate Start
£27k - £29k Annual
Full-Time
Talentmark are recruiting for an QA Administrator, to join a pharmaceutical company, based in Birmingham, on a permanent basis.
The salary is around £27,000-£29,000 per annum.
The Company:
Our client are a Pharma manufacturing company who produce, import, and distribute bespoke medicines (Specials), and CBPMs (Cannabis-Based Products for Medicinal Use).
Your main duties will be:
Manage the lifecycle of all controlled documents within the paper-based QMS (SOPs, forms, master documents, batch records, policies and specifications).
Provide administrative support for deviations, NCs, CAPAs, change controls, complaints and incident reports.
Ensure document activities comply with EU GMP (as applicable to Specials), MHRA expectations, and internal quality procedures.
Work closely with Production, QC and QA teams to ensure correct and timely use of controlled documents.
Design and execute method validation/verification, method transfers and robustness studies as required.
Your Background (Essential):
Degree in scientific, pharmaceutical or quality-related discipline.
Previous administration experience in an office or documentation-focused role.
Strong command in Microsoft Excel.
Your Background (Desireable):
Familiarity with core GMP documentation.
Experience in a GMP, pharmaceutical, specials or other regulated environment.
Knowledge of Specials Manufacturing regulatory requirements and MHRA guidance.
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
The salary is around £27,000-£29,000 per annum.
The Company:
Our client are a Pharma manufacturing company who produce, import, and distribute bespoke medicines (Specials), and CBPMs (Cannabis-Based Products for Medicinal Use).
Your main duties will be:
Manage the lifecycle of all controlled documents within the paper-based QMS (SOPs, forms, master documents, batch records, policies and specifications).
Provide administrative support for deviations, NCs, CAPAs, change controls, complaints and incident reports.
Ensure document activities comply with EU GMP (as applicable to Specials), MHRA expectations, and internal quality procedures.
Work closely with Production, QC and QA teams to ensure correct and timely use of controlled documents.
Design and execute method validation/verification, method transfers and robustness studies as required.
Your Background (Essential):
Degree in scientific, pharmaceutical or quality-related discipline.
Previous administration experience in an office or documentation-focused role.
Strong command in Microsoft Excel.
Your Background (Desireable):
Familiarity with core GMP documentation.
Experience in a GMP, pharmaceutical, specials or other regulated environment.
Knowledge of Specials Manufacturing regulatory requirements and MHRA guidance.
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: 225318340
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