Clean Room Operator

Quality Control Technician

The Quality Control Technician assists Quality Engineering, with inspection activities and key quality system activities. This role supports Quality Assurance personnel to ensure compliance with quality system regulations and contributes to business and continuous improvement initiatives. The ideal candidate is highly organized, detail-oriented, and persistent in following up to ensure actions are completed accurately and on time.

Key Responsibilities:

• Develop inspection sheets for implants, instruments, and associated components
• Draft first article inspection sheets for incoming inspection
• Develop overlays for optical comparators
• Write and route Engineering Change Orders (ECOs)
• Run, analyze, and publish reports related to site quality metrics
• Perform receiving, in-process, and final inspections
• Interpret engineering drawings and GD&T requirements
• Use measurement tools such as calipers, micrometers, gauges, and CMM equipment
• Support calibration activities and maintain equipment traceability
• Apply statistical techniques including SPC, Cp, and Cpk
• Utilize quality tools such as Pareto charts, control charts, and histograms
• Support structured problem-solving efforts (5 Whys, 8D, RCA)
• Manage nonconforming material and participate in Material Review Board (MRB) activities
• Support internal and external audits and corrective/preventive actions (CAPA)

Minimum Basic Qualifications:

• Minimum of 2 years of related experience and/or training
• Demonstrated ability to use computers effectively, including strong working knowledge of Microsoft
• Proficiency in mechanical inspection techniques and inspection equipment
• Experience tracking tasks, actions, or projects and following up to completion
• Ability to communicate clearly and professionally in written and verbal English

Travel Requirements:

• Up to 10% of travel may be required.

Desired Characteristics:

• Associate or bachelor's degree in engineering, science, or a related technical field (preferred but not required)
• Strong attention to detail with excellent analytical skills
• Experience in a regulated manufacturing environment (medical device experience is a plus)
• Ability to work collaboratively in a team-based environment
• Working knowledge of SolidWorks and overlay creation/printing

Physical Requirements:

• Must be able to lift 35 lbs.
• Must be able to stand long periods of time.
• Must be able to bend, twist and lift overhead.
• Must be able to pack & unpack boxes.

Currently, Enovis does not provide sponsorship for employment visas (e.g., H-1B) and will not offer such sponsorship in the future. Applicants must already have full-time work authorization in the United States, both now and in the future, without requiring sponsorship.