Senior Manufacturing Engineer

The ideal candidate will thrive on solving complex problems, identifying opportunities for efficiency, and contributing to a culture of continuous improvement.

• Collaborate with cross-functional teams and operational leaders to cultivate a continuous improvement culture, driving sustainable change and operational excellence.
• Enhance process performance by simplifying complex procedures, identifying waste, and optimizing existing manufacturing systems.
• Lead root cause analyses and implement robust, long-term technical or system solutions to address quality and process challenges.
• Develop and maintain preventive maintenance procedures for critical manufacturing equipment.
• Research and assess emerging process technologies to determine potential benefits and competitive advantages for implementation.
• Ensure that all products and processes meet stringent medical device quality and compliance standards.
• Resolve technical and quality issues efficiently to minimize impact on production and customer delivery.
• Work closely with the Production Support team to introduce process improvements, equipment upgrades, and product enhancements.
• Prepare and update manufacturing documentation and process specifications following established change control protocols.
• Ensure compliance with Health, Safety, and Environmental standards at all times.
• Identify, lead, and execute continuous improvement projects aimed at reducing waste, improving yield, and increasing efficiency.
• Support new equipment qualification and validation activities (EIQ/EOQ, DOE, OQ/PQ).

• Previous experience in medical device manufacturing is highly advantageous.
• Strong background in process troubleshooting and problem-solving methodologies.
• Proven ability to design, validate, and implement new manufacturing processes and equipment, working closely with suppliers or vendors.
• Capable of managing multiple projects simultaneously with effective planning and prioritization.
• Experience in jig and fixture design or maintenance is a plus.
• Working knowledge of Lean Manufacturing principles and statistical analysis tools.
• Familiarity with Minitab, SolidWorks, or AutoCAD software is desirable.
• Excellent interpersonal, communication, and organizational skills with a results-oriented mindset.
• Understanding of ISO and FDA regulatory compliance requirements for medical device manufacturing.

• Bachelor's Degree in Engineering or a related discipline.
• Minimum of 3+ years of relevant experience in a manufacturing or engineering environment, preferably within the medical device sector.