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- Tasks: Lead quality operations and certify pharmaceutical products in a regulated environment.
- Company: Established pharmaceutical manufacturer with a focus on quality and collaboration.
- Benefits: Competitive salary, benefits package, and long-term career development opportunities.
- Why this job: Make a real impact on quality systems and drive improvements in a growing organisation.
- Qualifications: Qualified Person status, degree in science, and 5 years in regulated pharma.
- Other info: Join a stable business with ongoing investment in people and operations.
The predicted salary is between 36000 - 60000 £ per year.
Cure Talent is delighted to partner with a well-established organisation in the pharmaceutical manufacturing sector who supply 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.
About the role
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.
Key responsibilities
- Certification and release of marketed and clinical product batches in line with current legislation
- Reviewing and approving batch documentation and GMP records
- 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
Key requirements
- 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
What’s on offer
- Senior quality 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. For more information or a confidential discussion, hit “Apply Now” to register your interest.
Qualified Person (QP) employer: Cure Talent
Contact Detail:
Cure Talent 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 sector and let them know you're on the hunt for a Qualified Person role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GMP compliance and recent changes in UK and EU legislation. We want you to be the go-to expert in the room, so practice articulating how your experience aligns with the responsibilities of the role.
✨Tip Number 3
Showcase your leadership skills! During interviews, share examples of how you've driven continuous improvement in quality systems. Highlighting your ability to influence quality culture will set you apart from other candidates.
✨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 about their job search.
We think you need these skills to ace Qualified Person (QP)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Qualified Person role. Highlight your experience in batch certification, GMP compliance, and any relevant qualifications. We want to see how your background aligns with what we're looking for!
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 senior quality leadership role. Share specific examples of how you've driven continuous improvement in previous positions.
Showcase Your Communication Skills: Strong communication skills are key for this role. In your application, demonstrate how you've influenced quality culture in past roles. We love to see candidates who can effectively engage with teams and stakeholders.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of your application and ensures you don’t miss out on any important updates. We can't wait to hear from you!
How to prepare for a job interview at Cure Talent
✨Know Your Legislation
Make sure you brush up on UK and EU legislation related to pharmaceutical manufacturing. Being able to discuss specific regulations and how they impact batch certification will show that you're not just familiar with the role, but that you’re also proactive about compliance.
✨Showcase Your Experience
Prepare to share concrete examples from your past roles where you've successfully navigated GMP compliance or led quality improvement initiatives. Use the STAR method (Situation, Task, Action, Result) to structure your responses and highlight your achievements.
✨Communicate Effectively
Strong communication skills are key for this role. Practice articulating your thoughts clearly and confidently, especially when discussing how you’ve influenced quality culture in previous positions. Remember, it’s not just what you say, but how you say it!
✨Prepare for Questions on Inspections
Since you'll be supporting MHRA and FDA inspections, be ready to discuss your experiences with these processes. Think about challenges you faced during inspections and how you overcame them, as well as any strategies you implemented to ensure ongoing audit readiness.
