Quality Manager - GMP Facilities & Equipment Qualification / Validation (FTC)

Haleon plc; Weybridge; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading consumer health company in Weybridge is seeking a Quality Manager to handle GMP facilities and equipment qualification. The successful candidate will lead validation activities, develop protocols, and ensure regulatory compliance. This role requires a Bachelor's degree in a scientific discipline and significant GMP experience. Excellent communication, analytical skills, and proficiency with validation tools are essential. This is a full-time position with an initial contract until the end of 2026.

Qualifications

• Significant experience in a GMP-regulated environment focusing on facilities and equipment qualification.
• Demonstrated knowledge of regulatory requirements and guidelines.
• Experience with risk-based approaches to validation and change management.

Responsibilities

• Lead and execute qualification and validation activities for facilities and equipment.
• Develop, review, and approve protocols, reports, and validation documentation.
• Support commissioning and qualification projects, including risk assessments.

Skills

Strong technical writing

Analytical skills

Problem-solving skills

Excellent communication

Interpersonal skills

Education

Bachelor’s degree in a scientific or engineering discipline

Tools

Validation software

Document management systems

MS Office Suite

Job description

Quality Manager - GMP Facilities & Equipment Qualification / Validation (FTC) page is loaded## Quality Manager - GMP Facilities & Equipment Qualification / Validation (FTC)locations: Weybridge – Headquarterstime type: Full timeposted on: Posted Todaytime left to apply: End Date: January 12, 2026 (24 days left to apply)job requisition id: 538696Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity. 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 full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.**Quality Manager - GMP - Facilities & Equipment Qualification / Validation****Initial fixed term contract until end of 2026****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**Job Posting End Date**2026-01-12## **Equal Opportunities**Haleon are 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’ll 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 (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity.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 full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.