ECIHighlight
Summary
About the Role
About You
- Bachelor's degree in Metrology, Life Sciences, or related field.
- 8+ years of experience in medical device manufacturing, product development, or technology transfer.
- Experience in metrology within a regulated medical device environment.
- Strong knowledge of GD&T and dimensional inspection techniques.
- Hands-on experience with CMM, VMM, CT scanning, and precision instruments.
- Experience supporting multi-site manufacturing transfers or consolidation projects.
- Familiarity with injection molding, extrusion, or secondary operations.
- Experience with Class I and Class II medical devices.
- Ability to travel between manufacturing sites as needed.
- Experience with plastics processing, such as molding and/or extrusion.
ECI (Enhanced Compliance Inc.) stands as a beacon of excellence in the life sciences consulting arena. With a dedicated team of industry professionals, ECI boasts a proven track record in full product lifecycle consulting for medical devices, pharmaceutical, biotech, and related industries. Our global consultants, with an average of 15 years of experience, provide top-tier quality, regulatory, and engineering solutions which are designed to cater to the unique needs of the dynamic life sciences market. Our team consists of highly skilled and specialized consultants with proven industry ability in FDA and international regulations, quality assurance and management, mergers and acquisitions due diligence, research and development support, regulatory affairs, post-market activities, technical services, manufacturing processes, product engineering, remediation, and project management. ECI's headquarters is in Marlborough, Massachusetts. We also have an operating office in Alajuela, Costa Rica, including a state-of-the-art packaging testing laboratory.