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- Tasks: Review analytical data and ensure compliance in a GMP-regulated environment.
- Company: Join LM Manufacturing, a leader in pharmaceutical quality assurance.
- Benefits: Enjoy competitive salary, generous leave, pension scheme, and free parking.
- Other info: Stable career growth opportunities in a supportive team environment.
- Why this job: Make a real impact on quality assurance in the pharmaceutical industry.
- Qualifications: Degree in Chemistry or related field; experience in QA or QC preferred.
The predicted salary is between 30000 - 40000 £ per year.
Weedon, Northamptonshire (NN7 4PP)
Competitive Salary (Depending on Experience)
Permanent | Full Time | Monday to Friday
Benefits:
- 21 days annual leave plus UK bank holidays, with additional annual leave for service (up to 4 extra days)
- Statutory pension scheme, 7 days paid sick leave, TOIL and free parking
- Stable long-term career opportunities and development support
Looking for a QA role in pharmaceutical manufacturing? Join LM Manufacturing as a QA Officer supporting analytical data review, compliance and quality systems within our GMP-regulated environment. This role sits within Quality Assurance and focuses on analytical data review, data integrity, investigations and compliance oversight, rather than hands-on laboratory testing.
Key Responsibilities:
- Review analytical data generated from QC testing of raw materials, in-process, finished products and stability samples
- Ensure compliance with ALCOA++ data integrity principles and GMP requirements
- Review data from HPLC, GC, UV, FTIR and related analytical systems
- Review and approve laboratory documentation, test reports and records
- Support and review investigations including OOS, OOT, deviations and CAPAs
- Contribute to root cause analysis and ensure quality of investigation reports
- Support Computer System Validation (CSV) and compliance of laboratory systems
- Participate in audits and ensure inspection readiness
What We’re Looking For:
- Degree in Chemistry, Pharmaceutical Sciences or related discipline
- Experience in QA, QC or analytical data review within pharmaceutical environments
- Strong understanding of GMP, data integrity and regulatory requirements
- Experience reviewing analytical data from HPLC, GC, UV, FTIR systems
- Strong experience in investigation review, report writing and root cause analysis
- Exposure to CSV, LIMS, Chromeleon or eQMS systems desirable
- Strong attention to detail and documentation skills
Why Join Us?
- Secure permanent employment
- Supportive quality team environment
- Opportunity to build a long-term career in Quality Assurance
- Work in a highly regulated pharmaceutical environment
Apply now to join our Quality Assurance team.
QA Officer – Analytical Review & Compliance employer: Northampton Business Directory
Contact Detail:
Northampton Business Directory Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Officer – Analytical Review & Compliance
✨Tip Number 1
Network like a pro! Reach out to people in the pharmaceutical industry, especially those working in QA roles. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GMP and data integrity principles. We want you to shine when discussing your experience with analytical data review and compliance oversight.
✨Tip Number 3
Showcase your attention to detail! Bring examples of your previous work where you’ve successfully reviewed analytical data or contributed to investigations. This will help us see how you fit into our quality team.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about joining our team.
We think you need these skills to ace QA Officer – Analytical Review & Compliance
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in QA and analytical data review. Use keywords from the job description to show we’re a perfect match for each other!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Share your passion for quality assurance and how your background aligns with our needs. Keep it concise but impactful.
Showcase Relevant Experience: When detailing your experience, focus on your work with GMP, data integrity, and any analytical systems like HPLC or GC. We want to see how you can contribute to our team!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity.
How to prepare for a job interview at Northampton Business Directory
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practices (GMP) and data integrity principles. Be ready to discuss how these apply to the role of a QA Officer, especially in relation to analytical data review. This shows you’re not just familiar with the terms but understand their importance in a pharmaceutical environment.
✨Showcase Your Analytical Skills
Prepare to talk about your experience with analytical systems like HPLC, GC, UV, and FTIR. Have specific examples ready where you’ve reviewed data or contributed to investigations. This will demonstrate your hands-on knowledge and how you can add value to their team.
✨Be Ready for Compliance Questions
Expect questions around compliance oversight and how you’ve ensured adherence to regulatory requirements in past roles. Think of scenarios where you’ve had to deal with OOS, OOT, or CAPAs, and be prepared to explain your thought process and actions taken.
✨Demonstrate Attention to Detail
Since this role requires strong documentation skills, be prepared to discuss how you ensure accuracy in your work. You might want to share examples of how you’ve maintained meticulous records or contributed to quality reports, highlighting your commitment to detail.