Overview
Regulatory Operations Associate – 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
As a Regulatory Associate, you’re at the forefront of shaping the synergy between our innovative products and the regulatory framework that guides them. Seeking a meticulous and proactive individual, this role offers you the chance to be the regulatory lead on pivotal projects, honing your communication skills, and nurturing robust partnerships — all while delivering critical tasks that influence our global presence. Your contributions will be impactful and meaningful, as you begin to navigate and influence the regulatory scenery that defines our industry.
Hiring Manager: Hannah Hussey
Closing Date: 21st August 2025
Your responsibilities
– Responsible for the delivery of high-quality submissions to agreed operations time frames and collaborating across partner functions to ensure timely delivery of all information required
– Apply previous experience with European and emerging market regulatory requirements to support global product strategies for new launches and market roll-out
– Ensuring all activities are performed in line with the operating model and internal best practice including the compliant use of all systems
– Partner with Regulatory Affairs and Safety (RAS) teams to develop, communicate, and implement regulatory strategies in collaboration with cross-functional project teams
– Maintain a strong understanding of internal business and regulatory processes to support operational efficiency
– Foster effective working relationships with regulatory partners and cross-functional stakeholders to enable seamless collaboration
The experience we're looking for
– Holds a degree in a relevant scientific discipline (e.g., Chemistry, Biological Sciences, Microbiology, Pharmacy)
– Knowledge of the self-care portfolio and regulatory requirements for marketing medicinal products
– Proven ability to manage multiple projects concurrently, with strong prioritisation and independent workload management
– Communicates effectively with stakeholders at all levels
– A results-oriented team player, committed to collaborative working and empathetic engagement across cross-functional teams
– Consistently delivers high-quality outputs within time and budget constraints, even under pressure
– Proficient in interpreting and summarising legislative requirements in both verbal and written formats
The skills for success
Task Execution Under Pressure, Business Acumen, Commercial Awareness, Objective Setting, Accountability, Consumer Insight, R&D, Product Lifecycle Management, Intellectual Property, Business Partnership, Collaboration and partnership building, Adapt to changes in technological development plans, Ability to challenge the status quo and propose improvement, Innovation Processes.
What we offer
Equality