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Qa officer – analytical review & compliance

Weedon (HP22 4)
L M MANUFACTURING LIMITED
Quality assurance officer
€37,000 a year
Posted: 17 May
Offer description

Check you match the skill requirements for this role, as well as associated experience.

Weedon, Northamptonshire (NN7 4PP)

Competitive Salary (Depending on Experience)

Permanent | Full Time | Monday to Friday


Benefits

* 21 days annual leave plus UK bank holidays, with additional annual leave for service (up to 4 extra days)
* Statutory pension scheme, 7 days paid sick leave, TOIL and free parking
* Stable long-term career opportunities and development support

Looking for a QA role in pharmaceutical manufacturing?

Join LM Manufacturing as a QA Officer supporting analytical data review, compliance and quality systems within our GMP-regulated environment.

This role sits within Quality Assurance and focuses on analytical data review, data integrity, investigations and compliance oversight, rather than hands‑on laboratory testing.


Key Responsibilities

* Review analytical data generated from QC testing of raw materials, in-process, finished products and stability samples
* Ensure compliance with ALCOA++ data integrity principles and GMP requirements
* Review data from HPLC, GC, UV, FTIR and related analytical systems
* Review and approve laboratory documentation, test reports and records
* Support and review investigations including OOS, OOT, deviations and CAPAs
* Contribute to root cause analysis and ensure quality of investigation reports
* Support Computer System Validation (CSV) and compliance of laboratory systems
* Participate in audits and ensure inspection readiness


What We’re Looking For

* Degree in Chemistry, Pharmaceutical Sciences or related discipline
* Experience in QA, QC or analytical data review within pharmaceutical environments
* Strong understanding of GMP, data integrity and regulatory requirements
* Experience reviewing analytical data from HPLC, GC, UV, FTIR systems
* Strong experience in investigation review, report writing and root cause analysis
* Exposure to CSV, LIMS, Chromeleon or eQMS systems desirable
* Strong attention to detail and documentation skills


Why Join Us?

* Secure permanent employment
* Supportive quality team environment
* Opportunity to build a long‑term career in Quality Assurance
* Work in a highly regulated pharmaceutical environment
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