R&D PDM Associate
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
This role sits within a dynamic and high-performing team responsible for delivering compliance projects across the Sore Throat Portfolio. The successful candidate will coordinate and support a range of R&D activities required to implement net revenue protection projects, including raw material changes, manufacturing process changes, analytical method development and validation, and medicinal licence maintenance.
This position offers a broad development opportunity for an early-career scientist to gain hands-on experience across multiple R&D disciplines. The role includes significant laboratory-based work, exposure to formulation development, analytical sciences, technical project leadership and regulatory dossier authoring. The associate will have the opportunity to build both technical expertise and project management skills while working within a cross-functional environment.
Your responsibilities
- Provide technical and analytical support for net revenue protection projects on medicinal products
- Plan, execute, and interpret laboratory studies to support product and process changes, method development, validation, troubleshooting, and continuous improvement activities.
- Develop and validate analytical methods in line with ICH Q2(R2), ICH Q14, internal procedures, and regulatory requirements.
- Support formulation and product development activities, including generating and interpreting data to support project decisions.
- Support technical workstreams and project activities to ensure delivery against agreed timelines and quality standards.
- Author and review technical protocols, reports, regulatory dossiers, and supporting documentation in accordance with current scientific, regulatory, and company requirements.
- Collaborate with global R&D, Quality, Regulatory, Supply, and Manufacturing teams to successfully deliver projects.
- Support investigation, troubleshooting, and resolution of technical challenges arising during project execution.
- Contribute to continuous improvement initiatives and support compliance, health & safety, and audit readiness activities across the wider team.
The experience we're looking for
- Degree in Chemistry, Pharmaceutical Sciences, Biological Sciences, or a related scientific discipline.
- Experience within an R&D, healthcare, pharmaceutical, or FMCG environment
- Strong scientific curiosity and a willingness to learn across multiple technical disciplines.
- Ability to analyse data, solve problems, and apply scientific reasoning to technical challenges.
- Excellent communication and collaboration skills.
- Strong organisational skills with the ability to manage multiple priorities.
- Self-motivated, proactive, and results-oriented with a focus on quality and compliance.
The skills for success
What we offer
Equality
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