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- Tasks: Lead exciting product development projects from concept to launch in the medical device sector.
- Company: Join a forward-thinking company dedicated to improving patient care and quality of life.
- Benefits: Enjoy competitive pay, professional growth opportunities, and a supportive team environment.
- Why this job: Make a real difference in healthcare while collaborating with diverse teams and innovative technologies.
- Qualifications: Experience in medical device development and strong communication skills are essential.
- Other info: Be part of a culture that values respect, diversity, and continuous improvement.
The predicted salary is between 36000 - 60000 £ per year.
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.
Duties and responsibilities
- Product Development Delivery
- 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.
- Cross-Functional Working
- 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.
- Quality & Regulatory Support
- Follow established design control and risk management processes.
- Contribute to design reviews, risk management files, and technical documentation.
- Support regulatory submissions by providing technical input, under the guidance of the Regulatory team.
- Continuous Improvement
- 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.
- Communication & Team Contribution
- 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.
Skills
- Essential
- Experience working in a regulated medical device product development environment.
- Experience delivering product development projects or defined workstreams.
- Working knowledge of medical device design controls and regulatory requirements.
- Strong organisational skills with the ability to manage multiple priorities.
- Clear, professional communication skills.
- Desirable
- 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.
Product Development Manager in Stevenage employer: Clinisupplies
Contact Detail:
Clinisupplies Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Product Development Manager in Stevenage
✨Tip Number 1
Network like a pro! Reach out to folks in the industry, attend relevant events, and connect with people on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its products. Understand their values and how they align with your experience in product development. This will help you show them you're not just a fit for the role, but for the team too!
✨Tip Number 3
Practice your pitch! Be ready to explain your past projects and how you've collaborated with cross-functional teams. Highlight your hands-on experience and how it relates to the role of Product Development Manager.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Product Development Manager in Stevenage
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Product Development Manager role. Highlight your experience in delivering product development projects, especially in regulated environments. We want to see how your skills align with our needs!
Showcase Your Collaboration Skills: Since this role involves working closely with various teams, emphasise your cross-functional collaboration experience. Share examples of how you've successfully worked with engineering, quality, and regulatory teams in the past.
Be Clear and Concise: When writing your application, keep it clear and to the point. Use professional language but don’t be afraid to let your personality shine through. We appreciate straightforward communication that gets to the heart of your experience.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Clinisupplies
✨Know Your Product Development Inside Out
Make sure you’re well-versed in the product development lifecycle, especially within the medical device sector. Brush up on design controls and regulatory requirements, as these will likely come up during your interview.
✨Showcase Your Cross-Functional Collaboration Skills
Be prepared to discuss examples of how you've worked with various teams like R&D, Quality, and Manufacturing. Highlight specific projects where you successfully collaborated to deliver results, as this role requires strong teamwork.
✨Prepare for Technical Questions
Expect questions that dive into your technical knowledge, especially around feasibility studies and risk management. Practise articulating your thought process and decision-making in past projects to demonstrate your expertise.
✨Emphasise Continuous Improvement Mindset
Share instances where you identified and implemented improvements in products or processes. This shows that you not only understand the importance of quality but are also proactive in enhancing performance.