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Process Quality Assurance; IPQA Officer

Job in Weedon Bec, NN11 3BH, England, UK
Listing for: LM Manufacturing
Full Time position
Listed on 2026-06-30
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Quality Engineering, Production QC/QA
  • Manufacturing / Production
    QA Specialist - Analyst/Manager, Quality Engineering, Production QC/QA
Salary/Wage Range or Industry Benchmark: 25396 - 28000 GBP Yearly GBP 25396.00 28000.00 YEAR
Job Description & How to Apply Below
Position: In-Process Quality Assurance (IPQA) Officer
Location: Weedon Bec

Overview

Weedon, Northamptonshire (NN7 4PP
)

£25,396.80 – £28,000 per annum + Shift Allowance

Permanent | Full Time

LM Manufacturing is seeking an In-Process Quality Assurance (IPQA) Officer to support our FDA and MHRA-approved pharmaceutical manufacturing facility.

Responsibilities
  • Perform in-process quality checks to ensure compliance with GMP, SOPs and batch manufacturing records
  • Monitor critical process parameters and verify manufacturing activities during production and packaging
  • Review batch manufacturing and packaging records for completeness, accuracy and compliance
  • Identify, document and support investigations relating to deviations and non-conformances
  • Support CAPA activities, root cause investigations and continuous improvement initiatives
  • Ensure compliance with GMP, hygiene, safety and quality standards throughout production
  • Support internal audits, customer audits and regulatory inspections
  • Work closely with Production, Quality Control, Engineering and Warehouse teams to maintain quality standards
What We're Looking For
  • Experience with in pharmaceutical manufacturing or quality assurance environments
  • Good understanding of GMP requirements and pharmaceutical quality systems
  • Strong attention to detail and documentation skills
  • Ability to review batch records and interpret technical information
  • Effective communication skills and the ability to work within cross-functional teams
  • Proactive and quality-focused approach
Desirable (Not Essential)
  • Experience in liquid pharmaceutical xlqdzyr manufacturing (oral liquids, syrups and suspensions)
  • Knowledge of MHRA, FDA and ICH regulatory requirements
  • Experience with deviation investigations and CAPA management
  • Degree in Pharmacy, Chemistry, Microbiology, Biotechnology, Life Sciences or a related discipline
Why Join Us?
  • Competitive salary plus shift allowance
  • Secure permanent employment with development opportunities
  • Opportunity to work in an FDA and MHRA-approved pharmaceutical manufacturing facility
  • Supportive Quality team and long-term career prospects
  • Be part of a company committed to Quality, Compliance and Patient Safety

Apply now to join our Quality Assurance team

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