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- Tasks: Lead QA operations and ensure compliance in a dynamic pharmaceutical environment.
- Company: Join a well-established pharmaceutical manufacturing company making a real impact.
- Benefits: Enjoy a hybrid work model with flexible on-site days and competitive perks.
- Why this job: This role offers hands-on leadership in quality assurance, perfect for career growth.
- Qualifications: Must be a qualified QP with 3-4 years of experience in GMP environments.
- Other info: Start date is ASAP; ideal for those ready to step up in their careers.
The predicted salary is between 36000 - 60000 £ per year.
Qualified Person (QP) – QA Operations Manager
Qualified Person (QP) – QA Operations Manager
2 weeks ago Be among the first 25 applicants
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QA Operations Manager & Qualified Person (QP)
Location: United Kingdom (Hybrid – 3 days on-site)
Industry: Pharmaceutical Manufacturing
Employment Type: Full-time
About the Role
We are partnering with a well-established pharmaceutical manufacturing company to hire a QA Operations Manager & Qualified Person (QP) to join their UK-based team. This is a key position supporting GMP compliance and sterile manufacturing operations, with direct responsibility for batch release and leadership of the site’s quality operations.
You’ll lead day-to-day QA activities, manage a small quality team, and ensure ongoing compliance with regulatory requirements. This hybrid role offers both strategic and hands-on responsibilities in a high-impact environment.
Key Responsibilities
- Act as Qualified Person (QP) for batch release of sterile pharmaceutical products
- Lead and mentor two QA Associates to ensure efficient and compliant operations
- Oversee QA processes, including deviation handling, CAPA, change control, and QMS updates
- Ensure site-wide GMP compliance and support audit readiness activities
- Represent QA during external inspections and audits (approximately 4–5 per year)
- Collaborate cross-functionally with manufacturing, supply chain, and regulatory teams
Required Qualifications
- Current eligibility to act as a Qualified Person (QP) in the UK
- 3–4 years of active QP experience
- Strong background in quality assurance within a GMP-regulated environment
- Experience in sterile manufacturing is essential
- Solid understanding of QMS, batch documentation, and regulatory requirements
- Prior experience managing or mentoring junior QA team members
- Ability to work on-site three days per week as part of a hybrid model
Preferred Qualifications
- Familiarity with MHRA and EMA regulatory expectations
- Experience representing QA during external audits or inspections
- Exposure to sterile fill/finish operations or aseptic processes
- Strong communication, leadership, and problem-solving skills
Additional Information
- Hybrid working model: minimum 3 days per week on-site
- Start date: ASAP (ideally within the next couple of months)
This is an excellent opportunity to lead quality operations in a dynamic and fast-paced sterile manufacturing environment. If you’re a Qualified Person ready for the next step in your career, apply today!
Seniority level
-
Seniority level
Mid-Senior level
Employment type
-
Employment type
Full-time
Job function
-
Job function
Quality Assurance and Manufacturing
-
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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Qualified Person (QP) – QA Operations Manager employer: Meet Life Sciences
Contact Detail:
Meet Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person (QP) – QA Operations Manager
✨Tip Number 1
Familiarise yourself with the latest GMP regulations and guidelines. Being well-versed in these will not only boost your confidence during interviews but also demonstrate your commitment to compliance and quality assurance.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who have experience as a Qualified Person. Engaging in conversations can provide you with valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples of how you've handled QA processes like deviation handling or CAPA in your previous roles. Real-life scenarios will showcase your problem-solving skills and leadership capabilities.
✨Tip Number 4
Research the company’s recent audits and inspections if available. Understanding their past challenges and successes can help you tailor your responses and show that you're genuinely interested in contributing to their quality operations.
We think you need these skills to ace Qualified Person (QP) – QA Operations Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience as a Qualified Person (QP) and your background in quality assurance within a GMP-regulated environment. Emphasise any leadership roles or mentoring experiences, as these are key for this position.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention specific experiences that align with the responsibilities listed, such as batch release processes and compliance with regulatory requirements.
Highlight Relevant Qualifications: Clearly state your eligibility to act as a Qualified Person (QP) in the UK and detail your 3–4 years of active QP experience. Include any familiarity with MHRA and EMA regulatory expectations, as well as your understanding of QMS and batch documentation.
Showcase Soft Skills: This role requires strong communication, leadership, and problem-solving skills. Provide examples in your application that demonstrate these abilities, particularly in cross-functional collaboration and during audits or inspections.
How to prepare for a job interview at Meet Life Sciences
✨Showcase Your QP Experience
Make sure to highlight your current eligibility and experience as a Qualified Person (QP). Discuss specific examples of batch releases you've managed and how you ensured compliance with GMP regulations.
✨Demonstrate Leadership Skills
Since this role involves leading a small QA team, be prepared to talk about your mentoring experiences. Share how you've guided junior team members and improved team efficiency in past roles.
✨Prepare for Regulatory Questions
Expect questions related to regulatory compliance, especially regarding MHRA and EMA expectations. Brush up on your knowledge of these regulations and be ready to discuss how you've navigated audits and inspections.
✨Emphasise Cross-Functional Collaboration
This position requires collaboration with various teams. Be ready to provide examples of how you've worked effectively with manufacturing, supply chain, and regulatory teams to achieve quality objectives.
