At a Glance
- 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.
- Why this job: Make a real impact on quality assurance in the pharmaceutical industry.
- Qualifications: Degree in Chemistry or related field; QA experience 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: L M MANUFACTURING LIMITED
At LM Manufacturing, we pride ourselves on being an excellent employer, offering a supportive and collaborative work culture that fosters professional growth and development. Located in Weedon, Northamptonshire, our QA Officer role provides a stable career path within the pharmaceutical industry, complete with competitive benefits such as generous annual leave, a statutory pension scheme, and opportunities for continuous learning in a GMP-regulated environment. Join us to be part of a dedicated team committed to quality and compliance, where your contributions will make a meaningful impact.
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 your connections in the pharmaceutical industry, especially those in QA roles. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GMP and data integrity principles. We recommend practising common interview questions related to analytical data review and compliance to show you're the right fit.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation and reiterate your interest in the QA Officer role. It keeps you fresh in their minds!
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our Quality Assurance 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 is tailored to the QA Officer role. Highlight your experience in analytical data review and compliance, and don’t forget to mention any relevant qualifications or skills that match the job description.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality assurance in the pharmaceutical industry and how your background makes you a perfect fit for our team at LM Manufacturing.
Showcase Your Attention to Detail:In QA, attention to detail is key. Make sure your application is free from typos and errors. This not only reflects your skills but also shows us that you take pride in your work.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets to us quickly and efficiently, plus you’ll find all the info you need about the role there!
How to prepare for a job interview at L M MANUFACTURING LIMITED
✨Know Your GMP and Data Integrity
Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP) and ALCOA++ data integrity principles. Be ready to discuss how these concepts apply to the role and share examples from your past experiences where you've ensured compliance.
✨Familiarise Yourself with Analytical Systems
Since the role involves reviewing data from HPLC, GC, UV, and FTIR systems, it’s crucial to understand how these systems work. Prepare to talk about your experience with these technologies and any specific challenges you’ve faced in data review.
✨Prepare for Investigation Scenarios
Expect questions around investigations, OOS, OOT, and CAPAs. Think of specific instances where you contributed to root cause analysis or wrote investigation reports. Being able to articulate your thought process will show your analytical skills.
✨Showcase Your Attention to Detail
In QA, attention to detail is key. Bring examples of how your meticulous nature has positively impacted your previous roles. Whether it’s through documentation or ensuring compliance, demonstrating this trait will resonate well with the interviewers.
