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- Tasks: Certify pharmaceutical batches and ensure compliance with regulations in a dynamic environment.
- Company: Global pharmaceutical leader committed to quality and patient safety.
- Benefits: Competitive salary, comprehensive benefits, and opportunities for professional growth.
- Why this job: Make a real impact on patient safety and quality in the pharmaceutical industry.
- Qualifications: Must be a qualified QP with experience in GMP and regulatory environments.
- Other info: On-site role in London with a collaborative team and career advancement opportunities.
The predicted salary is between 78000 - 102000 £ 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 City of London employer: Elvis Eckardt Recruitment
Contact Detail:
Elvis Eckardt Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person (QP) – Pharmaceutical Manufacturing & Quality in City of 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. A friendly chat can sometimes lead to job opportunities that aren’t even advertised!
✨Ace the Interview
Prepare for your interviews by brushing up on your technical knowledge and understanding the company’s values. Practice common interview questions and think of examples from your experience that showcase your skills as a Qualified Person. Remember, confidence is key!
✨Follow Up
After your interview, don’t forget to send a thank-you email! It shows your appreciation and keeps you fresh in their minds. Mention something specific from the interview to make it personal – it could give you the edge over other candidates.
✨Apply Through Our Website
Make sure to apply through our website for the best chance of landing that role! We keep an eye on applications that come directly through us, and it shows you’re genuinely interested in joining our team. Plus, it’s super easy to do!
We think you need these skills to ace Qualified Person (QP) – Pharmaceutical Manufacturing & Quality in City of 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 compliance 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 engagement to grab our attention.
Showcase Your Leadership Skills: We’re looking for someone who can lead cross-functional teams. Highlight any experiences where you’ve successfully led projects or initiatives in a pharmaceutical setting.
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 early in the process.
How to prepare for a job interview at Elvis Eckardt Recruitment
✨Know Your Regulations
Make sure you brush up on UK and EU pharmaceutical regulations, especially those related to GMP compliance and batch certification. Being able to discuss these confidently will show that you’re not just familiar with the rules but can also apply them in real-world scenarios.
✨Showcase Your Experience
Prepare specific examples from your past roles where you’ve successfully managed quality systems or led audits. Use the STAR method (Situation, Task, Action, Result) to structure your answers, making it easier for the interviewers to see your impact.
✨Engage with Cross-Functional Teams
Highlight your experience working with various departments like QA, Manufacturing, and Regulatory Affairs. Be ready to discuss how you’ve collaborated with these teams to enhance quality processes and ensure compliance, as this role requires strong cross-functional leadership.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s quality management systems and their approach to regulatory compliance. This not only shows your interest in the role but also gives you a chance to assess if the company aligns with your professional values and goals.
