In-Process Quality Assurance (IPQA) Officer
CV-LibraryNN7, Weedon Bec, West NorthamptonshirepermanentPosted: 18 June 2026
Apply NowIn-Process Quality Assurance (IPQA) Officer
📍 Weedon, Northamptonshire (NN7 4PP)
💷 £25,396.80 – £28,000 per annum + Shift Allowance
⏰ Permanent | Full Time
Shift Allowance
* £2,500 per annum (Day & Afternoon Shifts)
* £3,500 per annum (Night Shifts)
Benefits
* 21 days annual leave plus UK bank holidays, with additional annual leave based on length of service (up to 4 extra days)
* Statutory pension scheme, 7 days paid sick leave, Time Off in Lieu (TOIL) and free parking
* Full training and stable long-term career opportunities
Looking for a career in Pharmaceutical Quality Assurance?
Join LM Manufacturing as an In-Process Quality Assurance (IPQA) Officer supporting our FDA and MHRA-approved pharmaceutical manufacturing facility.
Key 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 within 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 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
📍 Weedon, Northamptonshire (NN7 4PP)
💷 £25,396.80 – £28,000 per annum + Shift Allowance
⏰ Permanent | Full Time
Shift Allowance
* £2,500 per annum (Day & Afternoon Shifts)
* £3,500 per annum (Night Shifts)
Benefits
* 21 days annual leave plus UK bank holidays, with additional annual leave based on length of service (up to 4 extra days)
* Statutory pension scheme, 7 days paid sick leave, Time Off in Lieu (TOIL) and free parking
* Full training and stable long-term career opportunities
Looking for a career in Pharmaceutical Quality Assurance?
Join LM Manufacturing as an In-Process Quality Assurance (IPQA) Officer supporting our FDA and MHRA-approved pharmaceutical manufacturing facility.
Key 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 within 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 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