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- Tasks: Lead the certification and release of medicinal products in a dynamic pharmaceutical environment.
- Company: Join a growing pharmaceutical company with a strong pipeline and established operations.
- Benefits: Enjoy a supportive, flexible work environment with a focus on quality and compliance.
- Other info: High visibility role with excellent opportunities for professional growth.
- Why this job: Make a real impact in the pharmaceutical industry while developing your career.
- Qualifications: Eligible QP status in the UK and significant GMP experience required.
The predicted salary is between 36000 - 60000 £ per year.
We are supporting a growing pharmaceutical company with a strong pipeline and established manufacturing operations, as they look to appoint a Qualified Person (QP) to join their Quality and Supply organisation. This is a permanent role offering long-term impact, high visibility, and an opportunity to contribute to both commercial and clinical product release in a specialist setting.
Key Responsibilities:
- Act as a named QP for the certification and release of licensed and investigational medicinal products
- Ensure all batches meet regulatory, GMP, and internal quality requirements prior to release
- Work closely with Quality Assurance, Manufacturing, Regulatory Affairs, and Supply Chain functions
- Participate in internal and external audits, including those by regulatory authorities
- Support continuous improvement of quality systems and manufacturing processes
- Provide expert guidance on GMP compliance and regulatory expectations across the site
Candidate Requirements:
- Eligible to act as a QP in the UK
- Significant GMP experience within pharmaceutical manufacturing, ideally across both clinical and commercial environments
- Excellent knowledge of quality systems, regulatory frameworks, and pharmaceutical supply chain requirements
- Strong communication skills and a collaborative working style
- Ability to operate effectively in a high-standard, fast-paced environment
What the Role Offers:
- The opportunity to play a key leadership role within a specialist pharmaceutical organisation
- Visibility across manufacturing, quality, and regulatory functions
- A supportive, flexible working environment with a strong focus on quality and compliance
Qualified Person in London employer: Nexia
Contact Detail:
Nexia Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person in London
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those at Nexia. A friendly chat can open doors and give you insights that a job description just can't.
✨Tip Number 2
Prepare for interviews by brushing up on your GMP knowledge and regulatory frameworks. We want you to shine when discussing how your experience aligns with the role of a Qualified Person.
✨Tip Number 3
Showcase your collaborative spirit! During interviews, share examples of how you've worked with Quality Assurance, Manufacturing, and Regulatory Affairs teams. It’s all about teamwork in this field.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative!
We think you need these skills to ace Qualified Person in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Qualified Person role. Highlight your GMP experience and any relevant certifications. We want to see how your skills match what we're looking for!
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 pharmaceuticals and how you can contribute to our team. Keep it concise but impactful!
Showcase Your Communication Skills: Since strong communication is key for this role, make sure your application reflects that. Use clear language and structure your documents well. We appreciate clarity and professionalism!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Don’t miss out on this opportunity!
How to prepare for a job interview at Nexia
✨Know Your GMP Inside Out
As a Qualified Person, you'll need to demonstrate a solid understanding of Good Manufacturing Practice (GMP). Brush up on the latest regulations and be ready to discuss how you've applied these in your previous roles. This shows you're not just familiar with the theory but can also implement it effectively.
✨Showcase Your Collaborative Spirit
This role requires working closely with various teams like Quality Assurance and Regulatory Affairs. Prepare examples of how you've successfully collaborated in the past. Highlighting your communication skills and teamwork will show that you can thrive in a fast-paced environment.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities in real-world situations. Think of specific instances where you had to ensure compliance or improve quality systems. Practising these scenarios will help you articulate your thought process clearly during the interview.
✨Ask Insightful Questions
At the end of the interview, have a few thoughtful questions ready about the company's quality systems or their approach to continuous improvement. This not only shows your genuine interest in the role but also gives you a chance to assess if the company aligns with your career goals.