Product Development Manager

The Product Development Manager will be responsible for delivering product development projects within the continence device portfolio. The role operates within an established product development framework and under the direction of senior leadership.

This is a hands‑on, mid‑level role focused on execution rather than strategy, suitable for an experienced product development professional who enjoys working closely with engineering, quality, regulatory, and manufacturing teams

• Deliver defined product development projects or work packages from concept through to launch, in line with agreed scope, timelines, and budgets
• Maintain accurate project documentation and development records in line with company procedures including product development plans & product specifications
• Support feasibility studies, design & development, verification, and validation activities with our internal manufacturing sites and external suppliers
• Implement approved design changes to existing products, including cost reduction and incremental performance improvements

• Work collaboratively with internal teams including R&D, Quality, Regulatory Affairs, Manufacturing, Supply Chain, and Marketing
• Work closely with Project Managers to ensure timely delivery of the projects
• Support engagement with clinicians, patients, and end users to inform product requirements and usability activities
• Coordinate day-to-day technical activities with suppliers and external partners

• Follow established design control and risk management processes
• Contribute to:
• Design reviews
• Technical documentation
• Support regulatory submissions by providing technical input, under the guidance of the Regulatory team.
• Identify and propose practical improvements to products, processes, and development activities
• Support early-stage concept generation and evaluation activities
• Stay informed on relevant developments within continence care and medical devices

• Provide regular, structured progress updates to the NPD team
• Highlight risks, dependencies, or delays in a timely manner
• Work closely and collaborate with our overseas teams in India and China
• Contribute positively to a quality-focused, patient-centred team culture
• Puts the consumer at the heart of decisions and improvement recommendations
• Upholds Clinisupplies’ Values and makes sure all colleagues feel valued, respected, appreciated and free to be who they are at work
• Complies with all policies, procedures, codes of ethics and mandatory instructions; identifies and reports risks
• Develops own capabilities and participates in development activities. Gains or maintains external professional accreditation where relevant to improve performance and fulfil personal potential
• Treats Clinisupplies funds carefully, ensuring they are not wasted and are utilised effectively
• Maintains accurate systems and records. Accesses, updates and deletes data for legitimate work purposes only. Takes appropriate steps to protect data, ensuring its accuracy and integrity

• Experience working in a regulated medical device product development environment
• Experience delivering product development projects or defined work streams
• Working knowledge of medical device design controls and regulatory requirements
• Strong organisational skills with the ability to manage multiple priorities
• Clear, professional communication skills
• Experience with continence, urology, or disposable medical devices
• Engineering background (mechanical, biomedical, or product design)
• Exposure to usability engineering or human factors
• Experience working with external suppliers or contract manufacturers