Role Overview
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.
Responsibilities
* Lead the Quality / Compliance activities for new product projects, supporting from initial concept to consumer during development and product transfer from R&D to site.
* Act as quality liaison and extended core team member for assigned projects, ensuring all functional Quality support is provided.
* Review and approve project‑related documents, including product specifications, batch documentation, test methods, analytical validation reports, method transfer, process and product transfer protocols, packaging documentation, and oversee Change Control, Deviation and CAPAs.
* Support clinical supplies activities, providing formal approval and release for clinical supplies, registration samples and consumer test supplies.
* Integrate customer and consumer insights into NPI projects, ensuring ongoing innovation and that products meet customer demands, and perform hyper‑care following launches.
* Provide leadership in quality compliance, partnering with R&D and QSC, building and maintaining effective collaboration, detecting potential issues early, resolving product challenges swiftly, and ensuring continuous improvement of product reliability, manufacturability, testing capabilities, and usability while maintaining compliance.
Qualifications
* Bachelor’s Degree in Pharmacy, Science, or equivalent level of knowledge, understanding and hands‑on experience in a regulated environment.
* Previous experience in the pharmaceutical industry related to Quality Assurance, Drug Regulatory Affairs, Technical Operations, or Drug Development in a GMP environment and manufacturing site experience.
Equal Opportunity
Haleon is an equal opportunity employer committed to a diverse and inclusive workplace. We value different backgrounds and perspectives and do not discriminate on the basis of race, color, religion, sex, gender identity, sexual orientation, age, disability, or any other protected characteristic. All employment decisions are made without regard to these factors.
Job Posting End Date
2026-06-26
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