R&D Quality Manager

We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. 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 Innovation & Product Lifecycle representative including MD Legal Manufacturer representative (when medical devices are in scope) , 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.
Lead the Quality / Compliance activities for new product projects, support from initial concept to consume 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
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.
Bachelor’s Degree in Pharmacy, Science, OR equivalent level of knowledge, understanding and hand on experience in a regulated environment

Minimum 5 years’ experience in the pharmaceutical industry related to Quality Assurance, Drug Regulatory Affairs, Technical
Operations, or Drug Development in a GMP environment
Excellent knowledge of key regulations, in addition to GMP, such as: ISO 13485, Medical Device Regulation 2017/745, Regulation 1223/2009 on cosmetic products and ISO 22716 – GMP Guidelines for Cosmetics
MS Office: good command
Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. 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.
Adjustment or Accommodations Request
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