In-Process Quality Assurance (IPQA) Officer

In-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