Overview
R&D Quality Manager, Compliance – 12 Month Fixed Term Contract (Kingston upon Hull, East Yorkshire, GB, HU1 1AA)
We are Reckitt
Research & Development
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
About the role
The R&D Quality Manager Audit Lead leads the R&D vendor approval for the clinical and quality compliance pillar within the Europe Vendor Quality Team. The role manages all activities associated with the audit programme and related documentation for GxPs (GCP, GVP, GMP) within R&D. The audit team provides support to global R&D colleagues, providing SME audit support when required.
The role may also be required to support supplier qualification and audit activities for the wider European Vendor Quality Team, Corporate Audits and related compliance activities for R&D Hull.
Hiring Manager – Jo Hodges
Closing Date – 9th February 2026
Location – Hybrid role, based in Hull with regular site presence.
Your responsibilities
- Management of External Compliance activities for R&D for all GxP and Core Reckitt products.
- Ability to collaborate with the global audit network to deliver the external audit programme and approve new vendors/ suppliers to R&D.
- Acts as an audit subject matter expert and support global R&D audit teams.
- Provide quality support for compliance activities including deviations, change controls and risk management relating to vendor quality management.
- Actively participates in quality culture and continuous improvement activities.
- Support the technology transfer process from R&D to commercial manufacture.
- Proactively monitors and responds to changes in guidance and legislation issued by Regulatory Authorities.
- Provides data and information to communicate supplier and supplier quality management performance at Quality Management reviews
- Requires travel to global Reckitt sites and 3rd party vendors.
- Ensure data integrity compliance.
- Support and ensure GxP systems are compliant to global policy and procedures and regulatory standards.
The experience we're looking for
- Trained and experienced lead auditor.
- Degree in a scientific discipline is required.
- Experience of working in a Quality environment for product development is essential.
- An appreciation and understanding of global medicines regulations is required.
- Previous line management experience is required.
- Ability to work cross functionally with global R&D teams and form collaborative relationships.
- Experience across a broad range of therapeutic areas and product classifications is desired.
- Ability to critically apprise Quality impacting regulatory guidance and legislation for internal action.
- Strong project management and organisational skills.
The skills for success
What we offer
Equality
IMPORTANT: Before applying for this role, please make sure you have the right to work in the country where the role is based. Unless it clearly stipulates within in the job advert above that the hiring company is looking to or able to sponsor applicants it is deemed that the hiring employer will only consider applications from those able to comply with and work in the country where the role is based.













