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- Tasks: Lead a team of Qualified Persons ensuring compliance and quality in radiopharmaceutical manufacturing.
- Company: Join a dynamic leader in the highly regulated pharmaceutical industry.
- Benefits: Enjoy competitive salary, career growth opportunities, and a supportive work culture.
- Why this job: Make a real impact on healthcare by ensuring the safe release of vital products.
- Qualifications: Must have 10+ years in Quality Assurance and be eligible as a Qualified Person.
- Other info: This role offers mentorship opportunities and the chance to shape national quality strategy.
The predicted salary is between 72000 - 108000 £ per year.
Are you a proven leader in pharmaceutical Quality Assurance with a strong background in QP oversight and team development? Do you have the vision and drive to lead Qualified Person operations across multiple sites, shaping strategic quality direction while mentoring high-performing teams? We are recruiting for a Senior QP Manager to take on a pivotal leadership role within a dynamic and highly regulated radiopharmaceutical manufacturing environment. This position offers the opportunity to lead a team of Qualified Persons, influence quality strategy at a national level, and ensure excellence in GMP compliance across UK operations.
About the Role
As a Lead QP, you will play a critical role in ensuring the safe release of radiopharmaceutical products across multiple sites in the UK. You will be responsible for:
- Managing and leading a team of permanent and contract Qualified Persons (QPs) across multiple UK manufacturing sites.
- Acting as a Releasing QP for radiopharmaceuticals/sterile products under a UK MHRA licence.
- Chairing the QP Forum and contributing to site Quality Management Meetings.
- Ensuring compliance with GMP, UK/EU regulations, and local/global procedures.
- Reviewing and certifying batches in a timely manner while overseeing deviations, complaints, CAPAs, and OOS/OOT investigations.
- Supporting MHRA inspections at key manufacturing sites.
- Acting as a mentor and coach for quality teams, fostering a culture of compliance and continuous improvement.
- Working closely with the Head of Quality to enhance and maintain the Global Quality System.
Experience & Qualifications
- Eligible to be named as a Qualified Person (QP) on a manufacturing licence.
- 10+ years’ Quality Assurance experience within a UK-licensed pharmaceutical organisation.
- 5+ years’ experience managing Quality teams in Quality Assurance or Quality Control.
- Previous experience in QP certification of medicinal products.
- Background in pharmaceutical manufacturing, preferably in sterile or radiopharmaceutical production.
Senior Qualified Person (QP) Manager employer: LinkedIn
Contact Detail:
LinkedIn Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Qualified Person (QP) Manager
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who have experience as Qualified Persons. Attend industry conferences or seminars to connect with potential colleagues and learn about the latest trends in Quality Assurance.
✨Tip Number 2
Showcase your leadership skills by participating in relevant forums or groups where you can share your insights on quality management. This not only demonstrates your expertise but also positions you as a thought leader in the field.
✨Tip Number 3
Familiarise yourself with the specific regulations and compliance requirements related to radiopharmaceuticals in the UK. Being well-versed in these areas will help you stand out as a candidate who is ready to take on the challenges of the role.
✨Tip Number 4
Prepare for interviews by thinking about how you would approach mentoring and developing high-performing teams. Be ready to discuss specific examples from your past experiences that highlight your ability to lead and inspire others in a regulated environment.
We think you need these skills to ace Senior Qualified Person (QP) Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in pharmaceutical Quality Assurance, particularly your leadership roles and QP oversight. Use specific examples that demonstrate your ability to manage teams and ensure GMP compliance.
Craft a Compelling Cover Letter: In your cover letter, express your passion for the role and the industry. Discuss your vision for leading Qualified Person operations and how your background aligns with the company's goals. Mention any specific achievements that showcase your capability in mentoring high-performing teams.
Highlight Regulatory Knowledge: Emphasise your understanding of UK/EU regulations and GMP compliance in your application. Provide examples of how you have successfully navigated regulatory challenges in previous roles, as this is crucial for the Senior QP Manager position.
Showcase Leadership Skills: Demonstrate your leadership skills by detailing your experience in managing Quality teams. Include examples of how you have fostered a culture of compliance and continuous improvement within your teams, as this will be key to the role.
How to prepare for a job interview at LinkedIn
✨Showcase Your Leadership Experience
As a Senior QP Manager, your leadership skills are crucial. Be prepared to discuss specific examples of how you've successfully led teams in the past, particularly in high-pressure environments. Highlight your ability to mentor and develop talent within your team.
✨Demonstrate Regulatory Knowledge
Familiarise yourself with GMP, UK/EU regulations, and any relevant local procedures. During the interview, be ready to discuss how you have ensured compliance in previous roles and how you would approach maintaining these standards across multiple sites.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities, especially regarding batch certification and handling deviations or complaints. Think of specific scenarios where you successfully navigated challenges and be ready to explain your thought process and outcomes.
✨Align with Company Values
Research the company’s mission and values, particularly their commitment to quality and safety in radiopharmaceuticals. Be prepared to articulate how your personal values align with theirs and how you can contribute to fostering a culture of compliance and continuous improvement.
