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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 focused on quality and compliance.
- Other info: Opportunity for visibility across key functions and excellent career growth.
- Why this job: Make a real impact in the pharmaceutical industry while developing your career.
- Qualifications: Must be eligible to act as a QP in the UK with significant GMP experience.
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
Seniority level: Mid-Senior level
Employment type: Full-time
Job function: Science, Quality Assurance, and Supply Chain
Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Research Services
Qualified Person in England employer: Nexia
Contact Detail:
Nexia Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person in England
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those already working at the company you're eyeing. A friendly chat can give you insider info and might even lead to a referral.
✨Tip Number 2
Prepare for the interview by brushing up on your GMP knowledge and quality systems. We want you to showcase your expertise confidently, so practice answering common questions related to the role.
✨Tip Number 3
Don’t forget to follow up after your interview! A quick thank-you email can keep you fresh in their minds and show your enthusiasm for the position. Plus, it’s just good manners!
✨Tip Number 4
Apply through our website for a smoother process. It’s designed to make things easier for you, and who knows, it might just give you an edge over other candidates!
We think you need these skills to ace Qualified Person in England
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 background aligns with the key responsibilities mentioned in the job description.
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. Mention specific experiences that demonstrate your knowledge of quality systems and regulatory frameworks, as these are crucial for us.
Showcase Your Communication Skills: Since strong communication skills are a must-have, make sure to highlight instances where you've successfully collaborated with different teams. We love seeing examples of how you’ve worked effectively in a fast-paced environment.
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 for the role. Plus, it shows you’re serious about joining our team!
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, don’t shy away from asking questions. Inquire about the company’s approach to continuous improvement in quality systems or how they handle regulatory audits. This not only shows your interest in the role but also your proactive mindset towards contributing to their success.