Quality Manager GMP Facilities & Equipment Qualification Validation (FTC) in Weybridge
Quality Manager GMP Facilities & Equipment Qualification Validation (FTC)

Quality Manager GMP Facilities & Equipment Qualification Validation (FTC) in Weybridge

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

  • Tasks: Lead qualification and validation activities for facilities and equipment in a GMP environment.
  • Company: Join Haleon, a purpose-driven consumer health company with a trusted brand portfolio.
  • Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
  • Why this job: Make a real impact on health by ensuring compliance and quality in innovative projects.
  • Qualifications: Bachelor's degree in science or engineering and experience in GMP environments required.
  • Other info: Dynamic role with excellent career advancement opportunities in a collaborative team.

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

Welcome to Haleon. We are a purpose-driven world-class consumer company putting everyday health in the hands of consumers. Our trusted portfolio of brands including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science. Now it’s time to fully realise the potential of our business and our people through our Win as One strategy.

Position Overview

This is an exciting new project-based role to support Haleon’s new R&D Facility in Weybridge. We are seeking an experienced Quality Manager with a strong background in facilities and equipment qualification and validation within a Good Manufacturing Practice (GMP) environment. The successful candidate will play a key role in supporting site compliance ensuring that all facilities, utilities, and equipment meet regulatory, corporate, and industry standards.

Key Responsibilities

  • Lead and execute qualification and validation activities for facilities, utilities, and laboratory equipment in accordance with GMP guidelines and site procedures.
  • Develop, review, and approve protocols (IQ/OQ/PQ), reports, and other validation documentation to ensure accuracy, completeness, and compliance with regulatory requirements.
  • Support commissioning and qualification projects including risk assessments and change control processes.
  • Collaborate with cross-functional teams (Engineering, Maintenance, Production, and Quality Control) to ensure timely completion of qualification and validation deliverables.
  • Participate in investigations, deviations, CAPAs, and root cause analysis related to qualification and validation issues.
  • Maintain validation master plans and schedules ensuring ongoing compliance and readiness for regulatory inspections.
  • Stay current with evolving industry standards, regulatory requirements (e.g. EMA, FDA), and best practices in validation and GMP compliance.
  • Support internal and external audits, responding to queries and providing documentation as required.

Qualifications & Experience

  • Bachelor's degree in a scientific or engineering discipline (e.g. Chemistry, Biology, Engineering) or equivalent relevant experience.
  • Significant experience in a GMP-regulated environment with a focus on facilities and equipment qualification and validation.
  • Demonstrated knowledge of regulatory requirements and guidelines.
  • Strong technical writing, analytical, and problem-solving skills.
  • Experience with risk-based approaches to validation and change management processes.
  • Excellent communication and interpersonal skills with the ability to work collaboratively across departments.
  • Proficiency with validation software, document management systems, and MS Office Suite.

Desirable Attributes

  • Experience in commissioning, qualification, and validation projects for new facility start-ups or expansions.
  • Familiarity with environmental monitoring, validation, and utility systems (HVAC, WFI, compressed gases, etc.).
  • Project management skills and the ability to prioritise tasks in a fast-paced environment.
  • Continuous improvement mindset and a proactive approach to compliance and operational excellence.

Location

This position is based onsite in Weybridge, UK.

Equal Opportunities

Haleon is committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture where different backgrounds and views are valued and respected, all in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people.

It’s important to us that Haleon is a place where all our employees feel they truly belong. During the application process, we may ask you to share some personal information which is entirely voluntary. This information ensures we meet certain regulatory and reporting obligations and supports the development, refinement, and execution of our inclusion and belonging programmes that are open to all Haleon employees. The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment decisions, including hiring decisions.

Adjustment or Accommodations Request

If you require a reasonable adjustment or accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please let your recruiter know by providing them with a description of specific adjustments you are requesting. We will provide all reasonable adjustments to support you throughout the recruitment process and treat all information you provide us in confidence.

Note to candidates

The Haleon recruitment team will contact you using a Haleon email account (@). If you are not sure whether the email you received is from Haleon, please get in touch.

Quality Manager GMP Facilities & Equipment Qualification Validation (FTC) in Weybridge employer: Gsk

At Haleon, we pride ourselves on being a purpose-driven employer that champions everyday health through our renowned brands. Our Weybridge location offers a collaborative and agile work culture, where employees are empowered to grow and innovate within a supportive environment. With a strong commitment to inclusion and continuous improvement, we provide ample opportunities for professional development, ensuring that every team member can thrive and contribute to our ambitious goals.
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Contact Detail:

Gsk Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Quality Manager GMP Facilities & Equipment Qualification Validation (FTC) in Weybridge

✨Tip Number 1

Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. 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 researching Haleon and understanding their values and mission. Tailor your responses to show how your experience aligns with their goals, especially in quality management and GMP compliance. This will help you stand out as a candidate who truly gets what they're about.

✨Tip Number 3

Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and boost your confidence. Focus on articulating your experience in facilities and equipment qualification, as well as your problem-solving skills in a GMP environment.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you're genuinely interested in joining Haleon and contributing to their mission of better everyday health.

We think you need these skills to ace Quality Manager GMP Facilities & Equipment Qualification Validation (FTC) in Weybridge

GMP Compliance
Facilities Qualification
Equipment Validation
Technical Writing
Analytical Skills
Problem-Solving Skills
Risk Assessment
Change Management
Cross-Functional Collaboration
Root Cause Analysis
Validation Documentation
Regulatory Knowledge (EMA, FDA)
Validation Software Proficiency
Project Management
Continuous Improvement Mindset

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Quality Manager role. Highlight your experience in GMP environments and any specific qualifications or validations you've managed. We want to see how your background aligns with our needs!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality management and how you can contribute to our mission at Haleon. Keep it concise but impactful – we love a good story!

Showcase Your Skills: Don’t forget to highlight your technical writing and problem-solving skills in your application. These are key for the role, so give us examples of how you've used these skills in past projects or challenges.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the details you need about the role and our company culture there!

How to prepare for a job interview at Gsk

✨Know Your GMP Inside Out

Make sure you brush up on Good Manufacturing Practice (GMP) guidelines before your interview. Be ready to discuss how you've applied these standards in your previous roles, especially in facilities and equipment qualification and validation.

✨Showcase Your Technical Skills

Prepare to talk about your experience with validation protocols like IQ, OQ, and PQ. Bring examples of documentation you've developed or approved, and be ready to explain your approach to risk assessments and change control processes.

✨Collaboration is Key

Haleon values teamwork, so think of examples where you've successfully collaborated with cross-functional teams. Highlight your communication skills and how you've worked with engineering, maintenance, and quality control to achieve compliance.

✨Stay Current with Industry Trends

Familiarise yourself with the latest regulatory requirements and best practices in validation and GMP compliance. Being able to discuss recent changes or trends will show that you're proactive and committed to continuous improvement.

Quality Manager GMP Facilities & Equipment Qualification Validation (FTC) in Weybridge
Gsk
Location: Weybridge

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  • Quality Manager GMP Facilities & Equipment Qualification Validation (FTC) in Weybridge

    Weybridge
    Full-Time
    36000 - 60000 £ / year (est.)
  • G

    Gsk

    10000+
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