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 the R&D PDM organisation and typically reports to an R&D PDM Senior Associate. It is designed to support the delivery of design work, risk management, and medical-device compliance activities within R&D PDM. While the primary responsibilities are outlined below, the role may also include additional tasks depending on organisational needs:
- Maintaining and updating the Design History Files for the IW portfolio during base-business projects.
- Coordinating and driving post‑launch reviews according to the agreed schedule.
- Providing subject‑matter expertise in medical devices to the wider R&D organisation and the business.
- Contributing to and executing project plans and other operational tools to ensure smooth delivery of base‑business projects.
- Identifying and solving problems, and determining best practices within medical‑device projects.
- Supporting the achievement and reporting of business KPIs and metrics relevant to the role
Your responsibilities
- Plan, manage, and deliver project and post‑market activities to meet agreed timelines and milestones.
- Provide medical‑device subject‑matter expertise to the R&D PDM team and the wider R&D organisation.
- Lead a small team to ensure all deliverables meet required standards.
- Support ongoing improvements in quality and efficiency across projects.
- Contribute to defining functional best practices and strategy within relevant areas.
- Ensure all product development and maintenance activities are completed according to agreed timelines, and promptly communicate any risks or issues to the line manager.
- Work with cross‑functional internal and external teams to ensure technical milestones are achieved.
- Ensure all required product specifications and internal documentation are complete, current, and fully approved prior to implementation.
- Demonstrate a strong consumer mindset by understanding behaviours across different regions and applying these insights to product design and development.
- Lead the preparation, approval, and distribution of design‑control and risk‑management documentation throughout the product development lifecycle.
- Ensure all assigned activities comply with legislative, health, safety, and environmental requirements.
- Support team operations, including shared activities such as audit preparation.
- Assist the Senior Associate in measuring, tracking, and reporting team KPIs to senior management
The experience we're looking for
- Minimum of an undergraduate degree in a scientific field relevant to the product technologies within the portfolio.
- Minimum of 3 years’ experience in either healthcare/FMCG product development or in the medical‑device industry, with focus on design control, risk management, or quality management.
- Experience in line management is preferred but not essential.
- Knowledge or experience in the following areas is preferred:
- ISO 13485 – Quality management systems for medical devices, especially product realisation.
- ISO 14971 – Risk management for medical devices, or other risk‑management methodologies (e.g., FMEA).
- BS EN 62366 – Usability engineering for medical devices.
- Design controls.
The skills for success
What we offer
Equality
Job Segment:
Medical Device, Nutrition, Counseling, Healthcare