R&D Quality Manager; FTC

Position: R&D Quality Manager (FTC - 12 months)
## R&D Quality Manager (FTC - 12 months)
Apply locations:
Weybridge St Georges Avenue time type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
June 26, 2026 (13 days left to apply) job requisition :
544743

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.

The purpose of this role is to manage the overall Quality and Compliance activities from initial concept to consumer for new product introduction and product lifecycle activities.

As the R&D Quality representative , this role is an extended core team member and performs the Quality activities in support of the NPI & Maintenance projects. He/she is the single point of contact for Quality during the development, transfer and launch of new products and in addition lifecycle compliance management.
** Key Responsibilities
** Lead the Quality / Compliance activities for new product projects, support from initial concept to consumer during the development and product transfer from R&D to site
* Extended core Team Member of assigned projects and Quality liaison for project from initial concept to consumer. Accountable to ensure all functional Quality support is provided to the project.
* Review and approve project related documents, including product specification, batch documentation, test method, analytical validation report, method transfer, process and product transfer protocol and reports and packaging documentation. Also oversee Change Control, Deviation, and CAPAs for assigned projects
* Support clinical supplies activities, including providing formal approval and release for clinical supplies, registration samples and consumer test supplies.
* Integration of customer and consumer insights effectively into NPI projects ensuring ongoing innovation and development addresses customer and consumer demands & perform Hypercare following launches
* Provide leadership in the area of quality compliance.
* Quality partner to R&D and QSC , building and maintaining effective collaboration , detecting potential issues early, resolving product challenges swiftly, ensuring continuous improvement in our products' reliability, manufacturability, testing capabilities, and usability while maintaining compliance
* Lead the Quality / Compliance activities for new product projects, support from initial concept to consumer during the development and product transfer from R&D to site
* Extended core Team Member of assigned projects and Quality liaison for project from initial concept to consumer . Accountable to ensure all functional Quality support is provided to the project.
** Knowledge/Education/Experience Required
*** Bachelor’s Degree in Pharmacy, Science, OR equivalent level of knowledge, understanding and hand on experience in a regulated environment
** Job-Related Experiences
*** Previous experience in the pharmaceutical industry related to Quality Assurance, Drug Regulatory Affairs, Technical Operations, or Drug Development in a GMP environment
* Manufacturing site experience.
** Job Posting End Date*
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