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- Tasks: Ensure quality and compliance in pharmaceutical manufacturing for clinical trials.
- Company: Join a specialist pharmaceutical organisation with a focus on innovation.
- Benefits: Competitive salary, collaborative culture, and opportunities for professional growth.
- Other info: Dynamic role with strong career advancement potential in a fast-paced environment.
- Why this job: Make a real impact in the pharmaceutical industry while working with cutting-edge technology.
- Qualifications: Must be eligible as a UK Qualified Person with GMP experience.
The predicted salary is between 60000 - 80000 £ per year.
Connected MedTech is partnering exclusively with a specialist pharmaceutical organisation to appoint a Qualified Person (QP) into a key role within its Quality function. Operating within a GMP-regulated manufacturing environment, the position will support the certification and release of pharmaceutical products manufactured for clinical trial supply. This opportunity offers the chance to join a growing pharmaceutical organisation with a strong technical focus, modern manufacturing capabilities and a collaborative approach across Quality, Manufacturing and Technical Operations.
The successful candidate will work closely with Quality, Manufacturing and Technical Operations teams, providing GMP expertise and supporting the ongoing development of quality and operational systems within a fast-paced manufacturing setting.
Key responsibilities:
- QP certification and release activities for products manufactured for clinical trial supply
- Supporting GMP compliance across manufacturing operations
- Participation in audits, inspections, investigations and CAPA activities
- Providing QA and regulatory guidance across technical teams
- Supporting quality system and operational improvement initiatives
About You
The ideal profile will include:
- Eligibility to act as a UK Qualified Person
- Significant experience working within UK GMP-licensed pharmaceutical manufacturing environments, particularly supporting IMPs and sterile products
- Strong stakeholder engagement and decision-making capability
- Ability to operate effectively within a collaborative technical environment
For further information or a confidential discussion, please get in touch.
Qualified Person (QP) in Nottingham employer: Connected MedTech
Contact Detail:
Connected MedTech Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person (QP) in Nottingham
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in GMP environments. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your GMP knowledge and recent trends in the pharmaceutical sector. We recommend practising common interview questions with a friend or using mock interview tools to boost your confidence.
✨Tip Number 3
Showcase your expertise! During interviews, be ready to discuss specific examples of how you've supported GMP compliance or improved quality systems in past roles. This will demonstrate your hands-on experience and problem-solving skills.
✨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 are proactive and engaged with our platform.
We think you need these skills to ace Qualified Person (QP) in Nottingham
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience in GMP-regulated environments. We want to see how your background aligns with the role of a Qualified Person, so don’t hold back on showcasing relevant skills and achievements!
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. We love seeing enthusiasm and a clear understanding of the responsibilities involved, so let your personality come through.
Showcase Your Stakeholder Engagement Skills: Since this role involves working closely with various teams, make sure to highlight your experience in stakeholder engagement. We want to know how you've successfully collaborated in the past and how you can bring that to our team.
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. Plus, it gives you a chance to explore more about us and what we do!
How to prepare for a job interview at Connected MedTech
✨Know Your GMP Inside Out
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Be ready to discuss how you've applied GMP principles in your previous roles, especially in relation to clinical trial supplies and sterile products.
✨Showcase Your Collaborative Spirit
Since the role involves working closely with various teams, prepare examples that highlight your ability to engage stakeholders and work collaboratively. Think of specific instances where your teamwork made a difference in quality or operational improvements.
✨Prepare for Audits and Inspections
Expect questions about your experience with audits and inspections. Be ready to share how you've handled these situations in the past, including any CAPA activities you've been involved in. This will demonstrate your hands-on experience and problem-solving skills.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions! Inquire about the company’s approach to quality system improvements or how they support their QPs in staying compliant. This shows your genuine interest in the role and the organisation.