Quality Manager - GMP Facilities & Equipment Qualification​/Validation; FTC

Quality Manager - GMP Facilities & Equipment Qualification / Validation (FTC) page is loaded## Quality Manager - GMP Facilities & Equipment Qualification / Validation (FTC) locations:
Weybridge – Headquarters time type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
January 12, 2026 (24 days left to apply) job requisition :
538696

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.
** 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…