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- Tasks: Lead QA operations and ensure compliance in pharmaceutical manufacturing.
- Company: Join a leading UK-based pharmaceutical manufacturer with a focus on quality.
- Benefits: Competitive salary, career development, and the chance to shape quality culture.
- Why this job: Make a real impact on product quality and compliance in a dynamic environment.
- Qualifications: Must be a UK Qualified Person with strong QA Operations experience.
- Other info: Opportunity to lead a small team and drive GMP standards.
The predicted salary is between 48000 - 72000 £ per year.
AssureBio is partnering with a UK-based pharmaceutical manufacturer to appoint an experienced Qualified Person (QP) who can also lead QA Operations at site level. This is a senior, hands-on Quality leadership role with full QP batch certification responsibility, broad GMP oversight, and the opportunity to shape quality culture across operations. If you’re a QP who enjoys being close to manufacturing, documentation, and people, this is a role where your judgement genuinely matters.
Responsibilities
- Certify and release finished pharmaceutical products in line with UK/EU GMP
- Provide senior QA oversight across manufacturing, testing, storage, and supply chain
- Lead QA Operations activity including batch documentation review, deviations, CAPAs, change control, and OOS
- Act as a key Quality advisor to senior leadership on product quality, compliance, and inspection readiness
- Support recalls, mock recalls, and regulatory interactions when required
From a QA Operations leadership perspective, you will:
- Manage and develop a small on-site QA team and coordinate with contract QPs
- Drive GMP standards through gemba walks, training, and QA presence on the shop floor
- Work cross-functionally with QC, Quality Systems, Operations, and Regulatory Affairs
- Maintain inspection readiness for MHRA and customer audits
- Ensure ongoing compliance with Marketing Authorisations and product quality systems
Key experience
- Eligible UK Qualified Person (QP)
- Strong background in QA Operations within pharmaceutical manufacturing
- Experience with non-sterile dosage forms
- Comfortable operating in regulated, fast-paced environments
- Proven ability to lead people, influence cross-functionally, and make risk-based decisions
- Confident communicator with strong documentation and technical writing skills
Qualified Person (QP) & QA Operations Manager in London employer: AssureBio
Contact Detail:
AssureBio Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person (QP) & QA Operations Manager in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the lookout for a QP role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your GMP knowledge and QA Operations experience. Be ready to discuss specific examples of how you've handled batch documentation, deviations, and CAPAs. Show them you’re the go-to person for quality assurance!
✨Tip Number 3
Don’t just apply anywhere—focus on companies that align with your values and career goals. Use our website to find roles that excite you and match your expertise. Tailor your approach to each company to stand out from the crowd.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Mention something specific from your conversation to show your genuine interest in the role and the company.
We think you need these skills to ace Qualified Person (QP) & QA Operations Manager in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience as a Qualified Person and in QA Operations. We want to see how your background aligns with the responsibilities mentioned in the job description, so don’t hold back on showcasing your relevant skills!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for this role. We love seeing genuine enthusiasm, so let us know what excites you about the opportunity to shape quality culture at AssureBio.
Showcase Your Leadership Skills: Since this role involves managing a small QA team, make sure to highlight your leadership experience. We want to know how you've influenced teams and driven GMP standards in your previous roles—give us the good stuff!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to keep track of your application and ensures you don’t miss out on any important updates. Plus, we love seeing applications come in through our platform!
How to prepare for a job interview at AssureBio
✨Know Your GMP Inside Out
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Be ready to discuss how you've applied these principles in your previous roles, especially in relation to batch certification and compliance. This will show that you’re not just familiar with the regulations but can also implement them effectively.
✨Showcase Your Leadership Skills
As a QP & QA Operations Manager, you'll need to lead a team. Prepare examples of how you've successfully managed and developed teams in the past. Highlight specific situations where your leadership made a difference, whether it was through training, mentoring, or driving quality improvements.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to quality assurance and compliance. Think about how you would handle deviations, CAPAs, or OOS results. Practising these scenarios can help you articulate your thought process and decision-making skills during the interview.
✨Communicate Clearly and Confidently
Strong communication is key in this role. Practice explaining complex concepts in simple terms, as you may need to advise senior leadership or collaborate with cross-functional teams. Being able to convey your ideas clearly will demonstrate your confidence and expertise.
