R&D Associate - Condoms ( 1 year Contract)
We are Reckitt
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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 an R&D Associate, you will play a key role in delivering product development projects across the Durex R&D portfolio. You will lead end-to-end (E2E) projects from concept through to market launch, or take ownership of a specific workstream within larger, more complex technical projects, depending on business needs. Your work will contribute directly to the development of innovative, consumer-preferred products and support their successful transition into full-scale production and commercial launch.
This role requires the ability to work independently while collaborating effectively within a multidisciplinary project team. You will be responsible for balancing project opportunities, costs, timelines, and technical constraints to deliver high-quality outcomes. Strong organizational, technical, and problem-solving skills are essential, along with the ability to take ownership of key project deliverables and drive progress in a dynamic environment.
The role may also involve coaching or line management responsibilities for R&D Assistants or junior R&D Associates. Success in this position requires both theoretical and practical expertise in relevant Durex technologies, such as formulation and process development, as well as a solid understanding of applicable regulatory and legislative requirements.
This is an exciting opportunity for someone who is passionate about innovation, enjoys solving technical challenges, and wants to make a meaningful impact through the development of products trusted by consumers around the world.
Your responsibilities
- Lead and execute product development activities in line with agreed project timelines, proactively identifying and escalating risks or issues to ensure successful delivery.
- Collaborate with cross-functional teams, both internal and external, to achieve technical milestones and project objectives.
- Plan, coordinate, and support factory trials, product qualification testing, and validation activities prior to commercialization.
- Ensure product specifications, technical documentation, and development records are accurate, complete, and approved before full-scale production.
- Provide guidance and support to R&D Assistants and junior Associates, including coaching and development opportunities where applicable.
- Apply consumer insights and market understanding to support the design and development of consumer-preferred products.
- Balance product performance, technical robustness, quality requirements, and cost targets throughout the development process.
- Develop and implement effective evaluation methodologies to support sustainable, consumer-relevant product claims.
- Contribute to idea generation, concept development, and continuous improvement initiatives.
- Ensure intellectual property (IP) considerations are appropriately assessed and addressed during product development.
- Prepare, review, and communicate technical reports and project updates throughout the product development lifecycle.
- Ensure all development activities comply with applicable regulatory, quality, safety, health, and environmental requirements.
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
- Results-oriented with strong planning, time management, and organizational skills, along with the ability to work independently and take initiative.
Experience working within large multinational organizations and complex cross-functional environments.
Adaptable and open to change, with the ability to challenge conventional thinking and generate innovative solutions. - Strong communication and stakeholder management skills, with the ability to perform effectively under pressure and manage competing priorities.
- A proactive and entrepreneurial mindset, coupled with a passion for innovation and continuous improvement.
- Strong analytical and problem-solving capabilities, with a structured approach to decision-making.
- Collaborative team player who builds strong working relationships across functions and cultures.
- Pilot plant, scale-up, or industrialization experience is advantageous.
- Global mindset with the ability to work across functional boundaries and develop a strong understanding of business and commercial objectives.
- Naturally curious, with a desire to explore new ideas, technologies, and opportunities to drive product innovation.
- Demonstrated ability to thrive in a fast-paced environment while consistently delivering high-quality results and meeting deadlines.
What we offer
Equality
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