Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead quality initiatives and ensure compliance in a dynamic pharmaceutical environment.
- Company: Join a global leader in sterile pharmaceutical production.
- Benefits: Competitive salary, career growth, and the chance to impact patient care.
- Why this job: Shape national quality functions and drive strategic decisions that matter.
- Qualifications: Must be a UK-registered Qualified Person with 5+ years in quality management.
- Other info: Collaborative culture with opportunities for mentorship and travel.
The predicted salary is between 48000 - 72000 ÂŁ per year.
Regional Quality Lead & QP
Location: North London
Type: Permanent
We’re looking for an experienced and driven Qualified Person (QP) to join a global leader in the production and supply of sterile pharmaceutical products. This is a high-impact leadership role within their UK operations, offering the opportunity to shape the national quality function, drive inspection readiness, and play a key role in strategic decision‑making that directly impacts patient care and business success. You’ll work closely with cross‑functional teams across their UK sites (Luton, Nottingham, North London) and collaborate with global quality and regulatory leaders to uphold the highest standards of safety, compliance, and operational excellence.
Key Responsibilities
- Act as a UK Qualified Person in accordance with Directive 2001/83/EC and UK Human Medicines Regulations.
- Lead and manage a team of 4 QA professionals, providing mentorship and strategic direction.
- Oversee batch release of sterile pharmaceutical products, ensuring full compliance with regulatory requirements.
- Develop and maintain robust quality systems and ensure continuous improvement initiatives.
- Conduct internal audits and support external regulatory inspections.
- Collaborate cross‑functionally with manufacturing, regulatory affairs, and supply chain teams.
- Drive quality culture across all sites and ensure alignment with corporate standards.
Requirements
- Must be a UK‑registered Qualified Person.
- Minimum 5 years’ experience in pharmaceutical quality management, ideally within sterile manufacturing.
- Strong leadership and team management skills.
- In‑depth knowledge of GMP, MHRA, and EU regulatory requirements.
- Willingness to travel regularly between Luton, Nottingham, and North London sites.
- Excellent communication, problem‑solving, and decision‑making abilities.
Quality, QA, audit, supplier, operational, QP, qualified, person, sterile, release, aseptic, radiopharmaceutical, radiopharmacy, manager, leader, supervisor, head, director
#J-18808-Ljbffr
Regional Quality Lead & QP employer: RBW Consulting LLP
Contact Detail:
RBW Consulting LLP Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regional Quality Lead & QP
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in quality management. 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 knowledge of GMP and regulatory requirements. We recommend creating a list of potential questions and practising your answers with a friend or mentor to boost your confidence.
✨Tip Number 3
Showcase your leadership skills! During interviews, share specific examples of how you've successfully managed teams or driven quality initiatives. This will help you stand out as a strong candidate for the Regional Quality Lead role.
✨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 and engaged in their job search.
We think you need these skills to ace Regional Quality Lead & QP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience as a Qualified Person and your leadership skills. We want to see how your background aligns with the key responsibilities mentioned in the job description.
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. Share specific examples of how you've driven quality initiatives and led teams in the past.
Showcase Your Regulatory Knowledge: Since this role involves compliance with regulatory requirements, be sure to mention your in-depth knowledge of GMP, MHRA, and EU regulations. We’re looking for someone who can hit the ground running!
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss any important updates from us!
How to prepare for a job interview at RBW Consulting LLP
✨Know Your Regulations
Make sure you brush up on the UK Human Medicines Regulations and Directive 2001/83/EC. Being well-versed in these regulations will not only show your expertise as a Qualified Person but also demonstrate your commitment to compliance and patient safety.
✨Showcase Your Leadership Skills
Prepare examples of how you've successfully led teams in the past. Highlight your mentorship experiences and how you've driven quality culture within your previous roles. This is crucial for a leadership position, so be ready to discuss your strategic direction and team management style.
✨Demonstrate Cross-Functional Collaboration
Think of specific instances where you've worked with manufacturing, regulatory affairs, or supply chain teams. Be prepared to discuss how you’ve navigated challenges in these collaborations and what impact it had on quality outcomes. This will show that you can effectively work across different functions.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving and decision-making abilities. Prepare for scenarios related to batch release compliance or internal audits. Practising your responses will help you articulate your thought process clearly and confidently during the interview.
