QA Lead & Qualified Person (QP)
QA Lead & Qualified Person (QP)

QA Lead & Qualified Person (QP)

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

  • Tasks: Lead quality assurance for sterile pharmaceuticals and manage a dedicated QA team.
  • Company: Growing pharmaceutical organisation with a focus on compliance and quality.
  • Benefits: Competitive salary, supportive environment, and career development opportunities.
  • Why this job: Make a real impact in the pharmaceutical industry while leading a passionate team.
  • Qualifications: Must be a UK-registered Qualified Person with 5 years of experience.
  • Other info: Regular travel between Luton, Nottingham, and North London for site oversight.

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

QA Lead & Qualified Person (QP)

Location: Luton (with regular travel to Nottingham and North London)
Industry: Sterile Pharmaceutical Products
Direct Reports: 4

About the Role:

We are seeking an experienced and dedicated QA Lead & Qualified Person (QP) to join a growing team, overseeing quality assurance activities across multiple sites. This is a pivotal role ensuring compliance with GMP standards in the manufacture of sterile pharmaceutical products. You will be based in Luton, with regular travel to our facilities in Nottingham and North London.

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.
  • 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.

What We Offer:

  • Competitive salary and benefits package.
  • Opportunity to lead quality operations across multiple sites.
  • Supportive and collaborative working environment.
  • Career development within a growing pharmaceutical organization.

Key Words:

Quality Assurance, QA, QP, Qualified Person, compliance, operations, operational, Lead, Manager, Head, Senior, Leadership, pharmaceutical, medicine, sterile, aseptic, compounding, biopharmaceutical, audit, auditor, batch release, GMP, cGMP

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QA Lead & Qualified Person (QP) employer: RBW Consulting LLP

Join a dynamic and supportive team as a QA Lead & Qualified Person (QP) in Luton, where you will play a crucial role in ensuring the highest standards of quality assurance across multiple sites. With a competitive salary and benefits package, along with ample opportunities for career development within a growing pharmaceutical organisation, you will thrive in a collaborative work culture that values mentorship and continuous improvement. Regular travel to Nottingham and North London adds variety to your role, making this an exciting opportunity for those looking to make a meaningful impact in the pharmaceutical industry.
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Contact Detail:

RBW Consulting LLP Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land QA Lead & Qualified Person (QP)

✨Tip Number 1

Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in quality assurance. 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 GMP knowledge and recent regulatory changes. We want you to showcase your expertise as a Qualified Person, so practice answering questions related to batch release and compliance.

✨Tip Number 3

Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation. It keeps you fresh in their minds and shows your enthusiasm for the role.

✨Tip Number 4

Apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about joining our team in Luton and beyond.

We think you need these skills to ace QA Lead & Qualified Person (QP)

Qualified Person (QP)
GMP Compliance
Leadership Skills
Team Management
Batch Release Oversight
Regulatory Knowledge (MHRA, EU)
Internal Audits
External Regulatory Inspections
Quality Systems Development
Continuous Improvement Initiatives
Cross-Functional Collaboration
Communication Skills
Problem-Solving Skills
Decision-Making Abilities
Willingness to Travel

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in pharmaceutical quality management and leadership. We want to see how your skills align with the QA Lead & Qualified Person role, so don’t be shy about showcasing your relevant achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality assurance in the pharmaceutical industry. We love seeing candidates who can articulate their motivation and fit for the role.

Showcase Your Regulatory Knowledge: Since this role involves compliance with GMP and other regulations, make sure to mention your in-depth knowledge of these areas. We’re looking for someone who can hit the ground running, so highlight any relevant certifications or experiences.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team at StudySmarter!

How to prepare for a job interview at RBW Consulting LLP

✨Know Your GMP Inside Out

Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Be prepared to discuss how you've applied these standards in your previous roles, especially in sterile manufacturing. This will show that you’re not just familiar with the regulations but can also implement them effectively.

✨Showcase Your Leadership Skills

As a QA Lead, you'll be managing a team of professionals. Think of examples where you've successfully led a team or mentored others. Highlight your leadership style and how it aligns with fostering a quality culture across multiple sites.

✨Prepare for Scenario-Based Questions

Expect questions that ask how you would handle specific situations, like an internal audit or a regulatory inspection. Prepare detailed responses that demonstrate your problem-solving skills and decision-making abilities, showcasing your experience in overcoming challenges in quality assurance.

✨Research the Company and Its Culture

Familiarise yourself with the company’s values and recent developments in their operations. Understanding their approach to quality assurance and how they align with corporate standards will help you tailor your answers and show that you're genuinely interested in being part of their team.

QA Lead & Qualified Person (QP)
RBW Consulting LLP

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