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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 and collaboration.
- Benefits: Competitive salary, career growth, and a dynamic work environment.
- Other info: Collaborative culture with opportunities for professional development.
- 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
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) employer: Connected MedTech
Contact Detail:
Connected MedTech Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person (QP)
✨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 or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your GMP knowledge and relevant regulations. We recommend practising common interview questions related to QP responsibilities, so you can showcase your expertise confidently.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation. It keeps you fresh in their minds and shows your enthusiasm for the role.
✨Tip Number 4
Apply through our website for the best chance at landing that QP role! We make it easy for you to showcase your skills and experience directly to employers looking for top talent like you.
We think you need these skills to ace Qualified Person (QP)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in GMP-regulated environments and any relevant qualifications. We want to see how your background aligns with the role of a Qualified Person, so don’t hold back on showcasing your expertise!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about the role and how your skills can contribute to our collaborative approach at StudySmarter. Keep it concise but impactful!
Showcase Your Stakeholder Engagement Skills: In your application, emphasise your ability to engage with various stakeholders. We value strong communication and decision-making skills, so share examples of how you've successfully navigated these relationships in past roles.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from our team!
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
This role requires working closely with various teams. Prepare examples of how you've successfully collaborated with Quality, Manufacturing, and Technical Operations in the past. Highlight your stakeholder engagement skills and decision-making capabilities.
✨Prepare for Audits and Inspections
Since participation in audits and inspections is part of the job, think about your experiences in these areas. Be ready to discuss how you've handled investigations and CAPA activities, showcasing your problem-solving skills.
✨Demonstrate Continuous Improvement Mindset
The company values operational improvement initiatives. Come prepared with examples of how you've contributed to quality system enhancements or operational improvements in your previous roles. This will show your proactive approach to quality assurance.