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- 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 is delighted to partner with a well-established organisation operating across pharmaceutical manufacturing and medical device combination products, supplying both commercial and clinical products to global markets.
Due to continued growth and investment across their operations, they are now looking to appoint a Qualified Person (QP). This is a senior role within Site Quality Operations, responsible for batch certification and providing quality leadership across manufacturing and operational teams in a highly regulated environment.
As Qualified Person, you will be named on the site’s Manufacturing Licences and take responsibility for the certification and release of finished and clinical products in line with UK and EU legislation. You will act as a senior quality leader on site, ensuring GMP compliance and driving continuous improvement across Quality systems and processes.
Developing and approving SOPs, validation documents, investigations, and change controls
* Supporting MHRA and FDA inspections and ongoing audit readiness
* Driving continuous improvement across site Quality systems and processes
* Providing GMP guidance and coaching to site teams
Qualified Person status under current UK legislation
* Degree in a relevant scientific discipline
* Strong working knowledge of cGMP in pharmaceutical manufacturing
* Experience participating in MHRA and FDA inspections
* At least 5 years’ experience within a regulated pharmaceutical environment
* Strong communication skills with the ability to influence quality culture
Senior quality xkybehq leadership role within a well-established manufacturing environment
* Opportunity to influence and improve site wide Quality systems
* Competitive salary and benefits package
* Long term career development within a growing organisation
* Collaborative and quality focused working culture
* Stable business with ongoing investment in people and operations
If you are a Qualified Person (QP) looking for a new challenge within a collaborative and quality driven environment, we would love to hear from you.
Qualified Person employer: Cure Talent Ltd
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
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.
