In-Process Quality Assurance (IPQA) Officer
Weedon, Northamptonshire (NN7)
£25,396.80 – £28,000 per annum + Shift Allowance
Permanent | Full-Time
Be part of the future of pharmaceutical manufacturing.
LM Manufacturing is an FDA and MHRA-approved pharmaceutical manufacturer and is currently undergoing an exciting transformation as part of the Zydus Group, one of the world's leading global life sciences organisations.
With continued investment in our people, facilities and technology, we are expanding our Quality team and are looking for an enthusiastic In-Process Quality Assurance (IPQA) Officer to help ensure our medicines continue to meet the highest quality and regulatory standards.
Whether you already have pharmaceutical QA experience or are looking to further develop your career in Quality Assurance, we'd love to hear from you.
What We Offer
✔ Competitive salary plus annual shift allowance
✔ 21 days annual leave plus Bank Holidays
✔ Additional annual leave with length of service (up to 25 days)
✔ Company pension
✔ Paid sick leave following successful probation
✔ Time Off in Lieu (TOIL)
✔ Free on-site parking
✔ GP On Demand service
✔ Employee Assistance Programme
✔ Ongoing training and career development
✔ Opportunity to work within an FDA & MHRA regulated pharmaceutical environment
✔ Stable long-term career within a growing international organisation
About the Role
As an IPQA Officer, you'll play a key role in ensuring products are manufactured in accordance with GMP, regulatory requirements and internal quality standards.
You'll work closely with Production, Quality Control, Engineering and Warehouse teams, providing quality oversight throughout the manufacturing process and helping to ensure every batch meets the highest standards before reaching patients.
Key Responsibilities
- Conduct in-process quality inspections throughout manufacturing and packaging.
- Verify manufacturing activities comply with GMP, SOPs and Batch Manufacturing Records.
- Review production documentation for completeness, accuracy and compliance.
- Monitor critical process parameters and identify potential quality risks.
- Raise and support investigations into deviations and non-conformances.
- Assist with CAPA implementation and continuous improvement initiatives.
- Support internal, customer and regulatory inspections.
- Promote a strong quality culture across the manufacturing site.
About You
You'll ideally have experience within a GMP-regulated manufacturing environment and enjoy working in a fast-paced, quality-focused setting.
Essential
- Experience within Pharmaceutical, Medical Device, Food, Chemical or other regulated manufacturing environments.
- Understanding of Good Manufacturing Practice (GMP).
- Excellent attention to detail.
- Strong documentation and record review skills.
- Good communication and teamwork skills.
- Ability to work shifts.
Desirable
- Pharmaceutical manufacturing experience.
- Oral liquid manufacturing experience.
- Experience reviewing Batch Manufacturing Records.
- Knowledge of MHRA and FDA requirements.
- Experience with Deviations, CAPA and Change Control.
- Degree in Pharmacy, Chemistry, Microbiology, Biotechnology or Life Sciences.
Why Join LM Manufacturing?
This is an exciting time to join our business.
As part of the Zydus Group, we are investing in our people, strengthening our Quality culture and expanding our manufacturing capability.
You'll have the opportunity to work alongside experienced pharmaceutical professionals, develop your technical expertise and build a long-term career within an international pharmaceutical organisation committed to improving patients' lives.
Right to Work
Applicants must have the legal right to work in the UK.
Unfortunately, we are unable to offer visa sponsorship for this position.
Apply Today
If you're passionate about quality, compliance and making a real difference to patients, we'd love to hear from you.
Join LM Manufacturing and help us deliver medicines that improve lives.
Pay: £25,396.80-£28,000.00 per year
Benefits:
- Company pension
- Free parking
- On-site parking
Work Location: In person
