QA Officer – Analytical Review & Compliance

Company: L M MANUFACTURING LIMITED
Apply for the QA Officer – Analytical Review & Compliance
Location: Weedon Bec
Job 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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Posted: May 17th, 2026