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Lead Production Engineer in Lenham

Job in Lenham, Maidstone, Kent County, ME14, England, UK
Listing for: Energy Jobline ZR
Full Time position
Listed on 2026-07-15
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 45000 - 50000 GBP Yearly GBP 45000.00 50000.00 YEAR
Job Description & How to Apply Below
Location: Lenham

Job Description

Salary: £45,000 - £50,000

Location: Harrietsham, Kent

Application and Interviews: The job advert closes by the 19th July 2026, with 1st stage telephone interviews and second stage face‑to‑face interviews scheduled to be held the last 2 weeks of July 2026.

The Story

Established in 1976, Bedfont is an award‑winning medical technology company based in Harrietsham, Kent. Its breath analysis medical devices are exported globally thanks to its network of carefully selected distributors.

The Challenge

Healthcare is evolving, and the market for breath analysis monitors is expanding. Bedfont is looking for hard‑working, like‑minded, and passionate individuals to join the Bedfont Family to help achieve its goal of innovating healthcare worldwide.

Benefits
  • 25 days paid holiday plus bank holidays
  • Social events
  • Private medical insurance
  • Subsidised health checks
  • Well‑being warriors
  • Well‑being garden and room
  • Annual optical allowance
  • Cycle to work scheme
  • Pension scheme
  • Bonus scheme
  • Hybrid working
  • Employee Assistance Programme (EAP)
  • Rewards and discounts platform
  • Referral bonus
  • Charity days
  • Home office setup allowance
  • Employee awards
  • Free on‑site parking
  • Training & development opportunities
  • Free uniform
  • Subsidised kids club
  • Subsidised Celler8 Devices
  • Time in service annual leave bonus
  • Enhanced Maternity and Paternity Pay
Mission

The Production Engineer is responsible for ensuring the successful transfer of products, technical documentation, and quality requirements from R&D into Operations, supporting the efficient and compliant manufacture of Bedfont's medical devices.

Roles and Responsibilities
  • Own and maintain the Device Master Record, ensuring all documentation is accurate, up to date, and subject to robust version control procedures.
  • Control the release, distribution, withdrawal, and archiving of technical documentation, ensuring only approved versions are available for operational use.
  • Ensure Purchasing and Supply Chain activities are aligned with the current approved DMR revision and associated technical specifications.
  • Lead New Product Introduction activities, including design transfer, pilot builds, manufacturing planning, and production readiness assessments.
  • Manage DMR control processes, ensuring technical files, revision histories, and document workflows are maintained in accordance with company and regulatory requirements.
  • Establish and maintain efficient manufacturing environments through the implementation of Lean manufacturing principles, 5S methodologies, cellular workflows, tooling, fixtures, and ESD controls.
  • Develop, maintain, and control manufacturing documentation, including work instructions, control plans, process documentation, and operator training records.
  • Coordinate and support process validation activities, including Installation Qualification, Operational Qualification, and Performance Qualification, ensuring compliance with quality and regulatory requirements.
  • Work closely with the Supply Chain Manager and Warehouse team to ensure Approved Vendor Lists, purchase order specifications, and incoming inspection requirements are effectively implemented and maintained.
  • Drive continuous improvement initiatives across Operations through the application of Lean Manufacturing, Six Sigma methodologies, Poka‑Yoke techniques, and structured problem‑solving approaches.
  • Review and approve the release of technical documentation to Operations and Supply Chain, ensuring all documentation is complete, accurate, and authorised prior to implementation.
  • Exercise authority to halt the implementation of manufacturing changes, production activities, or documentation releases where non‑compliance, quality concerns, or uncontrolled changes are identified.
  • Act as a key liaison between Research & Development, Quality, Purchasing, Supply Chain, Warehouse, and Production teams to ensure the effective transfer of products, processes, and technical information into manufacturing.
  • Provide technical guidance and support to operational teams to ensure manufacturing processes are implemented consistently, efficiently, and in accordance with quality standards.
  • Support business objectives by identifying opportunities to improve manufacturing…
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