/Executive Director

Executive Director

Charlton, MA, US, 01507Remoteusvia direct
// Job Type
Full Time
// Salary
USD 250,000 - 300,000/year
// Salary Range
250,000–300,000 USD / year
// Posted
1 month ago
// Seniority
director
// Work Mode
hybrid
// Experience
15+ manufacturing, 7+ leadership years

About the Role

Executive Director, Engineering - Site Manager Charlton/Franklin, MA Job Function:  Manufacturing Location:  Charlton, MA, US, 01507 Work Flexibility:  Hybrid Pay Range:  $250,000-$300,000 Job ID:  4881 Apply with account Apply now Location:  Onsite Charlton, MA & Franklin, MA (Open to relocation) | Up to 25% Travel  Division: Engineering Operations Base Compensation: $250-300k   Bonus / Performance Incentive: 35% on Base Auto Allowance: $7,200    Why you will love this role:   KARL STORZ is seeking an accomplished and visionary Executive Director of Engineering – Site Manager to lead our U.S. engineering and manufacturing operations. This role combines strategic oversight with hands-on leadership—driving innovation, operational excellence, and high-quality production across our Charlton and Franklin, MA facilities.   What you will be doing:    Lead North America–wide Process, Project, and Sustaining Engineering functions to ensure efficient, compliant, and cost-effective manufacturing. Serve as Site Leader for two MA manufacturing facilities—overseeing engineering, facilities, EHS, regulatory compliance, and financial performance. Champion continuous improvement, Lean, and Six Sigma initiatives, driving productivity and quality gains across teams and processes. Partner cross-functionally with R&D, Operations, and Quality to launch new products, transfer technologies, and strengthen process capabilities. Act as a key representative during audits and inspections, maintaining the highest standards of compliance and operational integrity. Inspire and develop teams, fostering a culture of innovation, accountability, and engagement.   What You Bring:   Bachelor’s degree in engineering or a related field; MBA preferred. 15+ years in manufacturing (medical device or regulated industry preferred) and 7+ years in multi-site leadership. Proven success in process optimization, automation, and product transfer initiatives. Strong understanding of FDA, ISO, and quality systems, with experience leading audits and CAPA activities. Exceptional communicator and strategic leader with a passion for talent development and operational excellence.

Tech Stack

engineeringmanufacturingprocess optimizationLean Six SigmaFDA complianceISO standardsCAPAteam leadershipoperations management

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