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Production Process Engineer

Job in Diseworth, Castle Donington, Leicestershire, DE74, England, UK
Listing for: Medstrom
Full Time position
Listed on 2026-07-17
Job specializations:
  • Manufacturing / Production
    Lean Manufacturing / Six Sigma, Manufacturing Engineer, Quality Engineering
  • Engineering
    Lean Manufacturing / Six Sigma, Manufacturing Engineer, Quality Engineering, Process Engineer
Salary/Wage Range or Industry Benchmark: 48000 GBP Yearly GBP 48000.00 YEAR
Job Description & How to Apply Below
Location: Diseworth

Production Process Engineer
Castle Donington, Derbyshire

Are you passionate about continuous improvement and process efficiency? Do you want to play a key role in helping a growing employee-owned manufacturing business achieve its lean, quality and productivity goals?

We are looking for an experienced Production Process Engineer to join our manufacturing team in Castle Donington, specialising in the assembly of medical equipment. This is a practical role for someone who is passionate about continuous improvement, lean manufacturing and developing efficient, world-class production processes.

The successful candidate will take ownership of the continuous improvement roadmap for production, proactively identifying opportunities to improve safety, quality, productivity, efficiency and cost. We are looking for someone who challenges existing ways of working, brings fresh ideas, and delivers measurable improvements rather than simply maintaining current processes.

The Benefits

- Starting salary in the region of £48,000, depending on experience
- Contributory pension scheme
- 33 days’ annual leave entitlement
- Discounts and cashback on shopping, supermarkets, and holidays
- Salary Sacrifice Schemes, including Cycle to Work
- Great training, support and mentorship
- Birthday gift
- Death in Service benefit provided
- Be a part of an Employee Ownership Trust (EOT) and the associated benefits of having a stake in the company

The Role

Your main responsibilities will be:

- Lead and own continuous improvement initiatives across the manufacturing operation and implement Lean Manufacturing tools, including 5S, Kaizen, Standard Work, Visual Management and Value Stream Mapping.
- Proactively identify opportunities to improve safety, quality, productivity, efficiency and cost.
- Develop and maintain manufacturing documentation, work instructions and standard operating procedures.
- Work closely with Production, Quality, Supply Chain and R&D to ensure products are designed for efficient manufacture and existing products continue to be improved.
- Investigate production issues, identify root causes and implement permanent corrective actions.
- Collaborate with Quality and R&D in the investigation of product issues, identification of root causes and implementation of permanent corrective actions.
- Monitor production data and KPIs to identify trends and drive measurable improvements; carry out time studies, line balancing and capacity analysis.
- Write specifications for tooling and production jigs and work closely with R&D on the design of these.
- Support engineering changes, product updates and design transfers into manufacturing.
- Support cost reduction projects, maintaining product quality and safety.
- Provide training to operators and team leaders.

Hours of Work: 37.5 per week, Monday - Friday, 8am - 4pm.

About You

Essential Requirements:

- Minimum 10 years' experience as a Process Engineer or Manufacturing Engineer within a manufacturing environment.
- Significant experience in an assembly manufacturing environment, preferably within the medical device or medical equipment industry.
- Proven experience implementing Lean Manufacturing principles and delivering measurable continuous improvement projects.
- Strong knowledge of Lean tools such as 5S, Kaizen, Value Stream Mapping, Standard Work and Root Cause Analysis.
- Demonstrable success in improving production lines, reducing waste, increasing productivity and improving quality.
- Excellent problem-solving, analytical and communication skills.
- Ability to influence change and work collaboratively across multiple departments.
- Engineering qualification (HNC/HND or Degree) or equivalent industry experience.

Desirable Requirements :

- Experience working within a regulated manufacturing environment (e.g. medical devices).
- Knowledge of PFMEA, Control Plans or similar quality improvement tools.

The recruitment process will consist of at least two interview stages, both of which will require attendance on site.

Candidates who progress to the final stage will be invited to complete either a practical assessment or a presentation, with the format to be confirmed prior to the final interview.

Why…
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