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