Senior Manufacturing Engineer

About the role

Vantedge Medical is a leading metals-based med-tech solutions provider. We specialize in precision engineering and innovation, serving top Medical Original Equipment Manufacturers (OEMs) globally. Our Continuous Improvement Engineer will drive efficiency, quality, safety, and cost-effectiveness through continuous improvement initiatives.

Responsibilities

• Identify Opportunities for Improvement
• Conduct thorough assessments of current manufacturing processes to identify areas for improvement.
• Analyze production data, quality metrics, and operational procedures to uncover inefficiencies and waste.
• Collaborate with cross-functional teams to gather insights and feedback on existing processes.
• Develop and Implement Improvement Strategies
• Design and develop innovative solutions to enhance productivity, reduce costs, and improve product quality.
• Lead the implementation of Lean Manufacturing, Six Sigma, and other continuous improvement methodologies.
• Develop and maintain standard operating procedures (SOPs) and best practices to ensure consistency and quality.
• Monitor and Measure Results
• Establish key performance indicators (KPIs) to measure the effectiveness of improvement initiatives.
• Monitor progress and provide regular reports to management on project status, outcomes, and areas for further improvement.
• Conduct root cause analysis for process deviations and implement corrective actions.
• Train and Mentor Staff
• Conduct training sessions for employees on continuous improvement techniques and methodologies.
• Mentor and guide team members in adopting a culture of continuous improvement and operational excellence.
• Foster a collaborative and proactive environment where employees feel empowered to contribute ideas for improvement.
• Ensure Compliance and Safety
• Ensure all improvement initiatives comply with industry standards, regulatory requirements, and safety guidelines.
• Collaborate with the Quality and Safety teams to ensure that all changes maintain or enhance quality and safety standards.

Requirements

• Education: Bachelor’s degree in Engineering, Quality Assurance, or a related field. Relevant certifications (e.g., CQE, Six Sigma) are a plus.
• Experience: Minimum of 5 years of experience in a manufacturing or quality engineering role, preferably within the precision machining or medical device industry. Demonstrated expertise in ISO 13485 is highly preferred.
• Skills: Experience with engineering tools and software. Proficiency in Microsoft 365 (Outlook, Word, Excel, PowerPoint, SharePoint, etc.).
• Language: Fluent in English.
• Other: Strong analytical and problem-solving skills, attention to detail, and the ability to work effectively in a fast-paced, collaborative environment.