LM Manufacturing
In-Process Quality Assurance (IPQA) Officer
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
In-Process Quality Assurance (IPQA) Officer
The experience expected from applicants, as well as additional skills and qualifications needed for this job are listed below.
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
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
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
Get help with your application
Your very own career expert that helps elevate your application to the next level.
Desirable (Not Essential)
Experience in liquid pharmaceutical xlqdzyr 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
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills