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For Companies At a Glance
- Tasks: Certify pharmaceutical batches and ensure compliance with regulations.
- Company: Global pharmaceutical leader focused on quality and patient safety.
- Benefits: Competitive salary, benefits package, and opportunities for professional growth.
- Why this job: Be the final authority ensuring safe medicines reach patients.
- Qualifications: Must be a qualified QP with relevant experience in pharmaceuticals.
- Other info: On-site role in London with a collaborative team environment.
The predicted salary is between 75000 - 85000 £ per year.
We are supporting a global pharmaceutical organisation operating in highly regulated UK and EU markets, seeking a Qualified Person (QP) to take full legal and technical ownership of batch certification, GMP compliance, and regulatory alignment across UK and European operations. This is a hands-on, accountable QP role where you act as the final legal authority between manufacturing and patient release.
What You'll Be Accountable For:
- Batch Certification & Manufacturing Oversight:
- Legally certify pharmaceutical batches in line with UK law and EU Directives
- Ensure manufacturing and testing activities comply with GMP and Marketing Authorisations
- Oversee internal and third-party manufacturing partners
- Quality Systems & Compliance Leadership:
- Own and maintain the Quality Management System (QMS)
- Lead governance of:
- Deviations
- CAPAs
- Change Controls
- Risk Assessments
- Annual Product Reviews (APR)
- Self-Inspections & Audits
- Regulatory & Authority Engagement:
- Act as a senior quality interface with MHRA and EU regulatory bodies
- Support inspections, manufacturing line approvals, and regulatory submissions
- Cross-Functional Leadership:
- Partner with QA, Manufacturing, Regulatory Affairs, and Supply Chain teams
- Lead GMP training and SOP development across UK/EU operations
- Quality Risk & Patient Safety:
- Own recall processes and escalation pathways
- Proactively identify and mitigate quality risks impacting patient safety
Must-Haves (Non-Negotiable):
- Eligible to act as a Qualified Person under UK law (Directive 2001/83/EC)
- 4–5+ years operating as a named QP in regulated pharmaceutical environments
- Degree in Pharmacy, Chemistry, Biology, or related life sciences
- Deep hands-on experience with:
- GMP manufacturing operations
- Batch certification and regulatory documentation
- Pharmaceutical Quality Systems
- Experience within large or multi-site pharmaceutical organisations
Nice-to-Haves:
- UK/EU multi-site manufacturing oversight
- Third-party manufacturer and Quality Agreement management
- Regulatory audit leadership
Work Environment:
- On-site role spanning manufacturing facilities and corporate quality office (London)
- Close collaboration with production, QA, regulatory, and leadership teams
- 2–3 stage interview process, including technical and compliance assessment
Compliance & Eligibility:
- UK Citizens / Permanent Right to Work required
Notice Period: 30–45 days preferred
This is a site-based role (not remote / hybrid).
Application Process:
To apply, please submit your CV and a cover letter detailing your relevant experience and qualifications for the role. Applications will be reviewed on a rolling basis, so early submissions are encouraged.
Equal Opportunity Employer: We value diversity and are committed to creating an inclusive work environment. We encourage applicants from all backgrounds to apply.
Contact: Elvis Eckardt
Qualified Person (QP) – Pharmaceutical Manufacturing & Quality in London employer: Different Technologies Pty Ltd.
Contact Detail:
Different Technologies Pty Ltd. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person (QP) – Pharmaceutical Manufacturing & Quality in London
✨Network Like a Pro
Get out there and connect with people in the pharmaceutical industry! Attend events, join relevant LinkedIn groups, and don’t be shy about reaching out to current employees at companies you’re interested in. We all know that sometimes it’s not just what you know, but who you know!
✨Ace the Interview
Prepare for those interviews by brushing up on your technical knowledge and understanding of GMP compliance. We recommend practising common interview questions and even doing mock interviews with friends or mentors. Show them you’re not just a qualified person, but the best person for the job!
✨Follow Up
After your interview, don’t forget to send a thank-you email! It’s a great way to express your appreciation and reiterate your interest in the role. We believe this small gesture can make a big difference in keeping you top of mind for the hiring team.
✨Apply Through Our Website
Make sure to apply through our website for the best chance of landing that Qualified Person role. We streamline the process and ensure your application gets the attention it deserves. Plus, it shows you’re serious about joining our team!
We think you need these skills to ace Qualified Person (QP) – Pharmaceutical Manufacturing & Quality in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience as a Qualified Person. Focus on your hands-on experience with GMP manufacturing and batch certification, as these are key for us.
Craft a Compelling Cover Letter: Your cover letter should tell us why you're the perfect fit for this role. Share specific examples of your achievements in quality systems and regulatory compliance to grab our attention.
Showcase Your Regulatory Knowledge: Since this role involves engaging with regulatory bodies like the MHRA, make sure to mention any relevant experiences you have with inspections or submissions. We want to see your expertise shine through!
Apply Early Through Our Website: Don’t wait until the last minute! Apply early through our website to ensure your application gets the attention it deserves. We review applications on a rolling basis, so get your materials in ASAP!
How to prepare for a job interview at Different Technologies Pty Ltd.
✨Know Your Regulations
Make sure you brush up on the UK and EU regulations relevant to pharmaceutical manufacturing. Being able to discuss specific directives, like Directive 2001/83/EC, will show that you’re not just familiar with the role but also understand the legal landscape you'll be operating in.
✨Showcase Your Experience
Prepare to share detailed examples from your past roles where you’ve successfully managed batch certification or GMP compliance. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your hands-on experience in regulated environments.
✨Engage with Cross-Functional Teams
Since this role involves collaboration with various teams, think of instances where you’ve worked closely with QA, Manufacturing, or Regulatory Affairs. Be ready to discuss how you’ve led training sessions or developed SOPs, as this will demonstrate your leadership capabilities.
✨Prepare for Technical Questions
Expect a mix of technical and compliance questions during the interview. Brush up on quality risk management and recall processes, and be prepared to discuss how you would handle specific scenarios related to patient safety and regulatory inspections.
