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Step into a high-impact engineering role where you’ll shape the future of electro-mechanical medical device manufacturing. My client is seeking a driven expert to lead process innovation, ensuring products are reliable, compliant, and built to the highest standards. This is your chance to influence life-enhancing technology at scale.
Why You Should Apply
Drive innovation in regulated medical device manufacturing
High-visibility role with cross-functional leadership impact
Hybrid work environment offering flexibility
Opportunity to lead complex, high-value engineering initiatives
Collaborate with top-tier engineering, quality, and regulatory teams
Amazing bonuses and stellar benefit package
What You’ll Be Doing
Lead manufacturing process improvements, validation, and optimization
Implement new equipment, automation, and process expansions
Troubleshoot complex production issues and drive root cause resolution
Partner with suppliers, CMOs, and internal teams to ensure product quality
Ensure compliance with FDA, ISO 13485, and global regulatory standards
Manage documentation, ECOs, and support regulatory submissions
About You
Bachelor’s degree in Engineering (Biomedical, Mechanical, Electrical, Industrial, or Manufacturing)
Strong expertise in process validation, statistical analysis, and quality systems
Deep understanding of FDA Design Controls and/or CE Mark requirements
Proven ability to lead complex engineering projects and process improvements
Familiarity with electro-mechanical device manufacturing environments
How To Apply
Send your resume to ava@scientificsearch.com and reference Job #19833.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Management and Manufacturing
Industries
Staffing and Recruiting
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