Job Summary :
The Senior Quality Technician is responsible for performing mechanical and visual inspections of procured materials, manufactured products, tooling, and processes to ensure compliance with IDEV and regulatory standards. This role supports manufacturing quality and process integrity by conducting first article inspections, maintaining documentation accuracy, and collaborating with engineering and quality leadership on inspection methods and issue resolution. Key Responsibilities :
- Perform routine and First Article inspections per IDEV drawings, specifications, and workmanship standards.
- Inspect incoming materials, in-process assemblies, and finished products for mechanical and visual compliance .
- Document Device History Records (DHRs) , log sheets, and inspection results accurately and on time.
- Identify, record, and process non-conformances for yield and trend analysis.
- Assist in developing and updating inspection procedures and routines .
- Train and mentor other inspectors or technicians in inspection techniques and equipment use.
- Collaborate with engineers and supervisors to recommend corrective actions and process improvements .
- Ensure compliance with FDA, ISO, and internal quality standards applicable to the medical device industry.
- Maintain a clean and organized work area in accordance with company safety and quality procedures.
Required Experience :
Minimum years of manufacturing experience in a production or quality role.Minimum years of inspection experience , preferably in the medical device or regulated manufacturing industry .Demonstrated ability to read and interpret engineering drawings, blueprints, and GD&T symbols .Experience using precision measurement tools and inspection equipment (, calipers, micrometers, gauges).Nice-to-Have Experience :
Certification as CMI (Certified Mechanical Inspector) or CQT (Certified Quality Technician) highly preferred.Prior experience documenting inspection results in ERP or MES systems .Required Skills :
Excellent verbal and written communication skills in English.Proficiency in Microsoft Excel, Word, and ERP systems for documentation and reporting.Strong attention to detail and data accuracy.Preferred Skills :
Ability to multi-task and work independently under limited supervision.Problem-solving and analytical skills in identifying root causes and corrective actions.Team collaboration in a cross-functional manufacturing environment .Education :
High school diploma or equivalent required.Technical or vocational coursework in manufacturing, metrology, or quality assurance preferred.Physical Requirements :
Must be able to lift up to lbs. and sit / stand for extended periods (– hours at a time).Frequent use of inspection tools requiring manual dexterity.Ability to visually inspect small and detailed components.Benefits :
Medical, Vision, and Dental Insurance Plans(k) Retirement FundAbout the Client :
A global healthcare innovator dedicated to improving lives worldwide through its diverse portfolio of medical devices, diagnostics, nutrition products, and branded generics . The organization is committed to developing technologies that address critical health challenges, advance care quality, and empower individuals to live healthier lives. Join the team and :
Work on cutting-edge healthcare and device technology projectsContribute to global quality and compliance initiativesExperience a culture of collaboration, inclusion, and excellenceBuild a rewarding career that makes a differenceAbout GTT :
GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. As a Native American-owned, economically disadvantaged corporation, we highly value diverse and inclusive workplaces. Our clients include Fortune banking, insurance, financial services, and technology companies, along with major life sciences, biotech, utility, and retail organizations across the and Canada. We look forward to helping you land your next great career opportunity! Job -
gttic gttjobs