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Quality Control Technician

Job in Austin, Travis County, Texas, 78716, USA
Listing for: Enovis
Full Time position
Listed on 2026-09-23
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Production QC/QA, Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 42000 - 64000 USD Yearly USD 42000.00 64000.00 YEAR
Job Description & How to Apply Below

Who We Are

Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company's extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond.

For more information about Enovis, please visit

What You'll Do

At Enovis we pay attention to the details. We embrace collaboration with our partners and patients, and take pride in the pursuit of scientific excellence - with the goal of transforming medical technology as we know it.

Because that's how we change the lives of patients for the better. And that's how we create better together. Why work at Enovis? See for yourself.

As a key member of the Quality Team, you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes.

Job Title:

Quality Control Technician

Reports To:

Sr Supervisor, Quality

Location:

Austin, Texas

Business Unit

Description:

The Quality Assurance business unitis responsible for ensuring all products meet internal quality standards and regulatory requirements. The team supports manufacturing operations by performing inspections, managing nonconformances, and driving continuous improvement to ensure product reliability and on‑time delivery

Job Title/High-Level

Position Summary:

The Quality Control Technician assists Quality  Engineering, with inspection activities andkey 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 andmaintainequipment traceability
  • Apply statistical techniques including SPC, Cp, andCpk
  • Utilize quality tools such as Pareto charts, control charts, and histograms
  • Support structured problem‑solving efforts (5 Whys, 8D, RCA)
  • Manage nonconforming material andparticipatein Material Review Board (MRB) activities
  • Support internal and external audits and corrective/preventive actions (CAPA)
Minimum

Basic Qualifications:
  • Minimum of2years 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'sdegree 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 Solid Works and overlay…
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