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- Tasks: Lead QP certification and ensure GMP compliance in a dynamic pharmaceutical environment.
- Company: Join a specialist pharmaceutical organisation with modern manufacturing capabilities.
- Benefits: Competitive salary, collaborative culture, and opportunities for professional growth.
- Other info: Engage with diverse teams and drive quality improvements in a fast-paced setting.
- Why this job: Make a real impact on clinical trial supplies and enhance your career in pharmaceuticals.
- Qualifications: Eligibility as a UK Qualified Person and experience in GMP-licensed environments.
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.
Lead Qualified Person employer: Connected MedTech
Contact Detail:
Connected MedTech Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Lead Qualified Person
✨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 roles, 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 a smoother process! We make it easy for you to submit your application and keep track of your progress. Plus, it shows you're keen on joining our team!
We think you need these skills to ace Lead Qualified Person
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight 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 the perfect fit for this role. Mention specific experiences that demonstrate your ability to support GMP compliance and your collaborative approach within technical teams.
Showcase Your Achievements: When detailing your experience, focus on your achievements rather than just responsibilities. We love to see quantifiable results, so if you’ve improved quality systems or led successful audits, make sure to highlight those successes!
Apply Through Our Website: We encourage you to apply through our website for a smoother application 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 Stakeholder Skills
Prepare examples that highlight your experience in engaging with various stakeholders. Think about times when you had to make tough decisions or collaborate across teams, and be ready to share those stories during the interview.
✨Be Audit-Ready
Since participation in audits and inspections is a key part of the role, come prepared with examples of your involvement in these processes. Discuss any CAPA activities you've led or contributed to, showcasing your problem-solving skills.
✨Demonstrate Your Collaborative Spirit
This role requires working closely with multiple teams, so be ready to talk about how you foster collaboration. Share instances where you’ve improved quality systems or operational initiatives through teamwork and communication.