More jobs:
Process Quality Assurance; IPQA Officer
Job in
Weedon Bec, NN11 3BH, England, UK
Listed on 2026-06-30
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
Job Description & How to Apply Below
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
- 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
- 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
- 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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