IPQA Officer (In-Process Quality Assurance)
Location: Weedon Bec, Northampton (NN7)
Reporting to: QA Manager
Shift Pattern: Rotating 3-shift pattern (24/7 operation), working 5 days out of 7
About LM Manufacturing Limited
LM Manufacturing Limited is a leading pharmaceutical manufacturer based in Weedon Bec, Northampton and is part of the Zydus Group, a global pharmaceutical company committed to improving healthcare through innovation, quality and patient care.
Our MHRA and FDA-approved manufacturing facility produces high-quality pharmaceutical products to the highest standards of Good Manufacturing Practice (GMP), quality, compliance and patient safety.
As part of our continued growth, we are looking for a motivated and detail-oriented IPQA Officer to join our Quality Assurance team.
What We Offer
- Competitive salary
- Shift Allowance
- £2,500 per annum for Morning & Afternoon shifts
- £3,500 per annum for Night shifts
- 21 days annual leave plus UK Bank Holidays
- Company pension scheme
- 7 days paid sick leave (following successful completion of probation)
- 5-month probation period
- Time Off in Lieu (TOIL) for approved overtime
- Free on-site and off-site parking
- Ongoing training and professional development
- Career progression opportunities within a growing pharmaceutical organisation
About the Role
Reporting to the QA Manager, you will play a key role in ensuring that manufacturing and packaging activities comply with Good Manufacturing Practice (GMP), regulatory requirements and internal quality standards.
You will provide in-process quality assurance support across manufacturing operations, carrying out line clearance, in-process checks, documentation review and real-time quality oversight to ensure products are manufactured in compliance with approved procedures.
The role supports our 24/7 manufacturing operation and operates on a rotating three-shift pattern, working 5 days out of every 7 days.
Key Responsibilities
- Perform line clearance activities before the commencement of manufacturing and packaging operations.
- Carry out routine in-process quality checks during manufacturing and packaging.
- Verify batch documentation for accuracy, completeness and compliance with Good Documentation Practice (GDP).
- Ensure manufacturing activities comply with approved SOPs, GMP and regulatory requirements.
- Monitor production processes and provide real-time quality support to manufacturing teams.
- Identify, document and escalate deviations, quality concerns and non-conformances.
- Support investigations, CAPAs and change controls where required.
- Ensure environmental, housekeeping and GMP standards are maintained throughout production areas.
- Support internal, customer and regulatory inspections and audits.
- Work closely with Production, QC, Warehouse, Engineering and Validation teams to maintain compliance and continuous improvement.
- Participate in training and quality improvement initiatives.
About YouEssential
- Degree, HNC/HND or equivalent qualification in a Life Science, Pharmaceutical Science, Chemistry or related discipline, or equivalent industry experience.
- Previous experience within Quality Assurance, IPQA or pharmaceutical manufacturing.
- Good understanding of Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP).
- Excellent attention to detail and documentation skills.
- Strong communication and interpersonal skills.
- Ability to work independently and make sound quality-based decisions.
- Flexible to work a 24/7 rotating three-shift pattern, working 5 days out of every 7 days.
Desirable
- Previous experience within an MHRA/FDA regulated pharmaceutical manufacturing environment.
- Knowledge of oral solid dosage (OSD) or oral liquid manufacturing processes.
- Experience with deviations, CAPAs, change controls and risk assessments.
- Experience using electronic quality systems or ERP systems such as SAP.
Shift Pattern
Supporting our 24/7 manufacturing operation:
- Morning: 5:45 am – 2:15 pm
- Afternoon: 1:45 pm – 10:15 pm
- Night: 9:45 pm – 6:15 am
Working 5 shifts out of every 7 days, including weekends as part of the rota.
Working Environment
- Pharmaceutical manufacturing facility.
- Production and packaging areas operating under GMP conditions.
- Regular interaction with cross-functional teams.
- Full PPE must be worn in designated manufacturing areas.
- Commitment to maintaining the highest standards of quality, compliance and patient safety.
Why Join LM Manufacturing Limited?
At LM Manufacturing Limited, you'll become part of a quality-driven organisation dedicated to manufacturing medicines that improve patients' lives. You'll have the opportunity to work within an MHRA and FDA-approved manufacturing facility, develop your technical and regulatory knowledge, and build a rewarding career within a growing pharmaceutical business.
LM Manufacturing Limited is an equal opportunities employer. We welcome applications from all suitably qualified candidates.
Pay: £26,496.80-£27,000.00 per year
Benefits:
- Company pension
- Free parking
- On-site parking
Work Location: In person
