Qualified Person

Qualified Person

Holmes Chapel Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Certify and release commercial batches while supporting QA and compliance projects.
  • Company: Join a leading pharmaceutical CDMO with a strong legacy in respiratory medicines.
  • Benefits: Collaborative team environment, opportunities for continuous learning, and potential for growth.
  • Why this job: Be part of an exciting growth phase and contribute to global health through quality assurance.
  • Qualifications: Must be a registered or eligible Qualified Person with pharmaceutical manufacturing experience.
  • Other info: Diverse backgrounds encouraged; this role supports both experienced and newly qualified professionals.

The predicted salary is between 36000 - 60000 £ per year.

Cure Talent are proud to be partnering with a leading pharmaceutical CDMO as they continue to invest in the development and expansion of their UK manufacturing site. With a strong legacy in respiratory medicines and device-based drug delivery, this site is entering an exciting new phase of growth. We’re looking to speak with both experienced and newly qualified QPs who are committed, driven and looking to take on a hands-on, commercially focused release role within a collaborative and well-established Quality function. You’ll join an established team of five QPs, reporting into a supportive QA leader. The team includes a mix of seasoned and newly qualified professionals, creating a balanced environment where knowledge-sharing and continuous learning are part of the culture. This role is a backfill for a long-serving QP retiring at the end of the year. As QP, you’ll be responsible for the certification and release of commercial batches for global markets. The number of batches per QP varies daily but typically averages 3–4, with the volume expected to grow next year as additional capacity comes online. A dedicated QA team handles the batch record reviews, allowing QPs to focus on decision-making, compliance and operational improvement. Key Responsibilities: * Certify commercial product batches in line with UK regulatory requirements. * Support QA with investigations, documentation, and compliance projects. * Contribute to site readiness for MHRA, FDA and customer inspections. * Play a role in continuous improvement initiatives and risk assessments. * Provide pragmatic input to cross-functional manufacturing and QA teams. * Support internal audits, technical changes and regulatory alignment. About You: * Registered or eligible Qualified Person under current UK legislation. * Background in pharmaceutical manufacturing is essential. * Experience in commercial release required; IMP or CDMO experience advantageous. * Open on dosage forms – broad experience or niche specialism welcome. * Confident decision-maker with a proactive, practical approach to quality. * Strong communicator with the ability to work both independently and as part of a team. * QPs from diverse backgrounds encouraged – as long as your experience extends beyond parallel imports. If you’re an experienced or newly qualified QP ready to take on a varied and rewarding role in a forward-thinking CDMO, we’d love to hear from you

Qualified Person employer: Cure Talent Ltd

Join a leading pharmaceutical CDMO that values collaboration and continuous learning, offering a supportive environment for both experienced and newly qualified Qualified Persons. With a strong focus on respiratory medicines and an exciting phase of growth at their UK manufacturing site, employees benefit from hands-on roles, opportunities for professional development, and a culture that prioritises knowledge-sharing and operational improvement. This is an excellent opportunity to contribute to global markets while being part of a dedicated team committed to quality and compliance.
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Contact Detail:

Cure Talent Ltd Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Qualified Person

✨Tip Number 1

Network with professionals in the pharmaceutical industry, especially those who work as Qualified Persons. Attend industry events or webinars to connect with potential colleagues and learn more about the company culture at the CDMO.

✨Tip Number 2

Familiarise yourself with the latest UK regulatory requirements for Qualified Persons. Being well-versed in these regulations will not only boost your confidence but also demonstrate your commitment to compliance during interviews.

✨Tip Number 3

Prepare to discuss specific examples of how you've contributed to quality assurance and compliance in previous roles. Highlighting your hands-on experience will show that you're ready to take on the responsibilities of this position.

✨Tip Number 4

Research the company's recent developments and growth plans. Understanding their focus on respiratory medicines and device-based drug delivery will help you tailor your conversations and show genuine interest in their mission.

We think you need these skills to ace Qualified Person

Qualified Person registration under UK legislation
Pharmaceutical manufacturing experience
Commercial batch release expertise
Knowledge of UK regulatory requirements
Experience with MHRA and FDA inspections
Strong decision-making skills
Proactive approach to quality assurance
Ability to support investigations and compliance projects
Cross-functional collaboration skills
Internal audit experience
Technical change management
Risk assessment capabilities
Effective communication skills
Teamwork and independent working ability

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your relevant experience in pharmaceutical manufacturing and commercial release. Emphasise any specific roles or projects that align with the responsibilities of a Qualified Person.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality assurance and your proactive approach to compliance. Mention your ability to work collaboratively within a team and your commitment to continuous improvement.

Highlight Relevant Qualifications: Clearly state your qualifications as a Registered or eligible Qualified Person under UK legislation. If you have experience with MHRA or FDA inspections, be sure to include that as well.

Showcase Soft Skills: In your application, highlight your strong communication skills and decision-making abilities. Provide examples of how you've successfully worked both independently and as part of a team in previous roles.

How to prepare for a job interview at Cure Talent Ltd

✨Know Your Regulations

Familiarise yourself with UK regulatory requirements for Qualified Persons. Be prepared to discuss how you ensure compliance in your previous roles, as this will demonstrate your understanding of the critical aspects of the job.

✨Showcase Your Experience

Whether you're newly qualified or experienced, be ready to share specific examples from your background in pharmaceutical manufacturing. Highlight any relevant experience with commercial release and how it aligns with the responsibilities of the role.

✨Emphasise Team Collaboration

Since the role involves working within a collaborative Quality function, be sure to express your ability to work well in teams. Share instances where you've contributed to team success or knowledge-sharing initiatives.

✨Prepare for Scenario Questions

Expect scenario-based questions that assess your decision-making skills and practical approach to quality. Think of examples where you've had to make tough decisions or implement improvements, and be ready to discuss the outcomes.

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