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Zimmer Biomet Holdings

Develops joint replacement, robotics, smart implants

Quality Assurance Technician Senior

Inspection & TestConfirmed live in the last 24 hours
Full-timeAustin, TX, USA$27 - $34 /hr

About the Job

Requirements

  • Have a high school diploma or equivalent with specialized training and/or certification and 4 years of relevant experience.
  • Have strong proficiency with precision measurement tools and inspection techniques.
  • Read blueprints and interpret geometric dimensioning and tolerancing to ASME Y14.5 or ISO 1101, including datums, feature control frames, position, profile, and runout.
  • Have hands-on metrology experience on any platform, with the judgment to select an appropriate method, build a repeatable setup, and recognize when a measurement is not trustworthy.
  • Maintain detailed documentation and organization.
  • Work effectively in a fast-paced research and development environment with evolving designs.
  • Have basic knowledge of statistical methods and inspection data analysis.
  • Have experience working to a formal, audited quality management system, such as ISO 13485, ISO 9001, AS9100, IATF 16949, ISO/IEC 17025, or a military or nuclear equivalent.
  • Meet the physical requirements of close visual acuity with correction, fine motor work, extended standing or bench work, and occasional lifting up to approximately 35 pounds; lift assists are available.

Responsibilities

  • Perform incoming, in-process, and final quality control inspection of research and development prototypes and development builds.
  • Conduct dimensional inspections using calipers, micrometers, height and pin gauges, gauge blocks, indicators, surface plate setups, optical comparators, surface-finish equipment, portable arm coordinate measuring machines, bridge coordinate measuring machines, vision systems, or laser scanning.
  • Interpret engineering drawings, geometric dimensioning and tolerancing, and specifications to verify prototype conformance.
  • Perform receiving inspection of supplier hardware, including review of certificates of conformance, material certifications, and first article reports.
  • Support design verification and validation builds with measurement data, build-unit traceability, and configuration records.
  • Generate and document inspection reports, measurement data, and nonconformance records.
  • Own the research and development metrology lab, including equipment setup and qualification, calibration scheduling and tracking, and environmental monitoring.
  • Partner with engineers on measurement data analysis and improve inspection methods as designs evolve.
  • Ensure compliance with quality system requirements and documentation standards.
  • Work day shift Monday through Friday, with flexibility around build and test milestones; there are no rotating shifts or regular weekend coverage.
  • Work in a hands-on laboratory and engineering development setting with precision instruments and prototype hardware.
  • Complete structured onboarding with a named mentor from the Quality team and defined competency sign-offs.
  • Complete training on ISO 13485, FDA 21 CFR Part 820 / QMSR, design controls, and nonconformance and corrective and preventive action processes.
  • Complete paid original equipment manufacturer training on the portable coordinate measuring machine and measurement software, company-sponsored geometric dimensioning and tolerancing coursework, and support toward ASQ or ASME GDTP certification.

Desired Qualifications

  • Medical device experience is preferred but not required.
  • Associate degree or technical certificate in manufacturing, quality, or engineering technology is a plus.
  • A machinist, tool and die, or metrology apprenticeship; a trade school certificate; or military technical training in precision measurement or calibration is a plus.
  • Prototype, new product introduction, low-volume build-to-print, job shop, tooling qualification, or test lab experience is highly desirable.
  • Medical device quality systems (ISO 13485, 21 CFR Part 820 / QMSR) and design controls; FARO arm operation and CAM2 / PolyWorks; nonconformance and corrective and preventive action records; calibration program administration; and handling and packaging requirements for surgical instruments are nice to have.
  • Familiarity with ASME Y14.5, ISO 10360, ANSI/NCSL Z540.3, ISO/IEC 17025, ISO 13485, or an equivalent audited quality system such as ISO 9001, AS9100, IATF 16949, NQA-1, or MIL-STD is a plus.
  • Certifications such as ASQ CQI/CQT, ASME GDTP, NIMS, original equipment manufacturer coordinate measuring machine training, or military calibration / PMEL are a plus.

About the Company

Zimmer Biomet Holdings

Develops joint replacement, robotics, smart implants

Zimmer Biomet manufactures and markets musculoskeletal medical devices and instruments for joint replacement, surgical trauma, and sports medicine. Its products include joint implants, surgical tools, and smart implants, often supported by robotic-assisted surgery systems. The company develops, produces, and sells these devices and provides services such as medical education and training to healthcare professionals to support procedures and outcomes. Compared with competitors, Zimmer Biomet benefits from a long history (over 90 years), a global footprint, and a focus on integrated solutions that combine advanced implants with robotics technology and education partnerships. Its goal is to advance patient care by delivering reliable devices, technologies, and professional training that improve surgical outcomes and collaboration with healthcare providers.

Company size
10,001+
Company stage
IPO
Headquarters
Warsaw, IN
Founded
1927

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