Editorial summary

The company, a well-established multinational corporation specializing in the design and manufacturing of advanced medical devices, is seeking an Engineering Manager (FDA) Process Improvement to lead their manufacturing engineering team. The role involves resolving complex production and technical issues, ensuring compliance with medical device quality and regulatory standards, and driving New Product Introduction activities. The position offers a salary of 14,000 and is located in the North or West region, with easy accessibility. Candidates should possess strong leadership skills and experience in manufacturing process development within the medical device industry.

This summary is AI-generated and may contain inaccuracies. Please refer to the full job description below.

Job description

[This job id 19316 first appeared in Job-Q.com on 11 Jul 2026]

Our client is a well-established MNC specializing in the design and manufacturing of advanced devices. Due to their current expansion plan, they are looking for an Engineering Manager to lead their manufacturing engineering team. They are located in the (North / West) – easily accessible.

Responsibilities:

• Lead the Manufacturing Engineering team in resolving complex production and technical issues while ensuring compliance with medical device quality and regulatory standards.
• Drive New Product Introduction (NPI) activities, including process development, manufacturing readiness, and successful product transfer into production.
• Oversee process optimization, automation initiatives, and continuous improvement projects to enhance manufacturing efficiency, quality, and productivity.
• Collaborate with cross-functional teams to support product development, engineering changes, manufacturing improvements, and customer requirements.
• Develop and implement engineering solutions to improve product reliability, process capability, and manufacturing performance.
• Evaluate new manufacturing technologies, equipment, and automation solutions to strengthen operational capabilities.
• Ensure engineering activities comply with ISO 13485, regulatory requirements, and internal quality management systems.
• Monitor engineering projects, manufacturing performance, and process improvements to achieve operational and business objectives.

Requirements:

• Degree in Engineering or related discipline.
• 5+ years of Class III medical device manufacturing experience, catheter experience is an advantage.
• Experience in NPI and process development.
• Strong experience in manufacturing automation and process improvement.
• Familiar with ISO 13485 and medical device regulations.

Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/CV.

We regret that only shortlisted candidates will be notified.

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