Kimal
Product Development Engineer
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Location: Hybrid – Bromsgrove and Worcester
Reports to: Head of CRP Product Management
At Kimal, we believe success is built through collaboration, shared values, and a commitment to making a difference. Our values of Integrity, Positivity, Inclusion, and Kindness are at the heart of everything we do, creating an environment where people can thrive, contribute, and grow.
We are looking for a Product Development Engineer to join our team and play a key role in developing and improving our Procedure Pack product range. This is an exciting opportunity for an engineer who enjoys solving technical challenges, evaluating innovative products, and working collaboratively across multiple disciplines.
You will support products from initial concept and technical evaluation through to validation, integration, and manufacture, helping ensure our products meet the highest standards of quality, safety, and regulatory compliance.
The Opportunity
Working closely with Product Management, Purchasing, Quality, Regulatory, and Manufacturing, you will help identify, assess, and integrate components and devices from external suppliers into our Procedure Pack range.
You will combine your engineering expertise with a practical understanding of materials, manufacturing processes, and design controls to support new product introductions, improve existing products, and drive continuous improvement across the business.
What You Will Be Doing
- Develop and specify products: Translate design inputs into clear engineering requirements, product specifications, and technical documentation.
- Support new product introduction: Work cross-functionally to evaluate, validate, and introduce new products from concept through to pre-launch.
- Evaluate components and suppliers: Assess third-party components, materials, and medical devices against technical, quality, and regulatory requirements.
- Drive product improvement: Identify alternative components and support cost-reduction, product consolidation, and continuous improvement initiatives.
- Manage technical documentation: Maintain product specifications, drawings, bills of materials (BOMs), data sheets, and design history files in line with applicable regulatory requirements.
- Ensure compliance: Support engineering processes and design control activities in accordance with relevant Medical Device Regulation (MDR) and ISO 13485 requirements.
- Support manufacturing: Work with suppliers and manufacturing teams to assess product feasibility, cost, manufacturability, and design for manufacture.
- Solve technical problems: Investigate manufacturing issues, quality concerns, and field complaints, supporting root cause analysis, corrective actions, and design changes.
- Contribute to risk management: Support product risk assessments and provide technical input into regulatory submissions.
- Collaborate and communicate: Provide technical expertise to Product Management and work with internal teams, suppliers, clinicians, and other external stakeholders.
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What We Are Looking For
You will be a practical, analytical, and detail-oriented engineer who enjoys working in a collaborative, regulated environment. You will be comfortable balancing technical requirements with product performance, quality, cost, and manufacturing considerations.
Essential Qualifications and Experience:
- A degree in Engineering, such as Mechanical, Biomedical, Materials Engineering, or a related discipline.
- Proven experience in product development or design engineering.
- Working knowledge of materials, fabrics, and plastics used in medical device or Procedure Pack manufacturing.
- Proficiency in 3D parametric CAD software, such as SolidWorks or equivalent, and an understanding of technical drawing standards.
- Practical knowledge of manufacturing processes and design for manufacture.
- Experience with design control processes, including design inputs and outputs, verification, validation, and risk management.
- Full UK driving license.
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Desirable Experience:
- Experience working within the medical technology sector or another regulated industry.
- Knowledge of MDR and ISO 13485 design control requirements.
Why Join Kimal?
At Kimal, you will be part of a collaborative team where your engineering expertise will contribute to the development and improvement of medical products used in clinical settings.
You will have the opportunity to work across the product lifecycle, collaborate with a broad range of technical and commercial specialists, and help deliver products that meet demanding quality and regulatory standards.
Benefits
- Competitive salary
- 25 days’ annual leave + 8 bank holidays
- Option to purchase an additional 2 days’ leave.
- Competitive pension scheme
- Life Assurance
- Discounted gym membership
- Employee discounts and wellbeing platform
- Healthcare Plan
- A supportive, values-driven working environment
Working Arrangements
This role offers a hybrid working model, with regular attendance required at our Bromsgrove office and Worcester head office. Occasional travel to other business locations may also be required.
Interested?
If you’re an engineer with a passion for product development, technical problem-solving, and continuous improvement, we’d love to hear from you.
Join Kimal and help us develop and deliver high-quality medical products through engineering excellence, collaboration, and innovation.
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