QA Officer – Analytical Review & Compliance
CV-LibraryNN7, Weedon Bec, West NorthamptonshirepermanentPosted: 23 April 2026
Apply NowQA Officer – Analytical Review & Compliance
📍 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
Apply now to join our Quality Assurance team
📍 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
Apply now to join our Quality Assurance team