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Capstan Medical

Quality Assurance Technician – In-line

Capstan Medical

. Perform in-line inspections of surgical robotic components in accordance with approved procedures and specifications .

Posted 11/3/2026full-timeSanta Cruz • California • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in quality inspection processes within the medical device industry, with a strong focus on surgical robotic components and adherence to Good Manufacturing Practices (GMP). Proficient in documentation practices and effective communication to support quality assurance initiatives.

Highest-signal resume keywords
Quality InspectionGood Manufacturing Practices (GMP)Device History Records (DHRs)Nonconformance Reports (NCRs)Surgical Robotic Devices

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Quality InspectionDocumentation PracticesVisual InspectionDimensional InspectionQuality Systems KnowledgeAttention to DetailData EntryCompliance VerificationProblem ResolutionInspection Procedures
Soft Skills
Verbal CommunicationWritten CommunicationTeamworkAttention to DetailEffective Communication
Tools & Technologies
Electronic Quality SystemsMicrosoft OfficeInspection Tools
Industry Keywords
Medical Device IndustrySurgical RoboticsElectromechanical DevicesQuality AssuranceManufacturing Processes

About the role

Key responsibilities & impact
  • Perform in-line inspections of surgical robotic components in accordance with approved procedures and specifications
  • Conduct product label and packaging inspections to verify accuracy and compliance with approved procedures and requirements
  • Inspect returned devices and document findings in accordance with established processes
  • Review Device History Records (DHRs) for completeness, accuracy, and compliance
  • Identify and document nonconforming materials or processes and initiate Nonconformance Reports (NCRs) as required
  • Quarantine and control movement of nonconforming material
  • Support investigation and resolution of quality issues with Manufacturing and Engineering teams
  • Represent Quality Assurance on the manufacturing floor and provide real-time quality guidance
  • Maintain accurate inspection records and ensure timely data entry into quality systems
  • Adhere to safety procedures and Good Manufacturing Practices (GMP)

Requirements

What you’ll need
  • Excellent verbal and written communication skills
  • AA degree or equivalent directly transferable work experience
  • Minimum of 3 years of professional experience working in quality inspection or manufacturing within the medical device industry
  • Preference for experience working with surgical robotic or other electromechanical devices
  • Familiarity with inspection tools and techniques, including visual and dimensional inspection
  • Working knowledge of quality systems, documentation practices, and GMP requirements
  • Strong attention to detail and ability to follow written procedures
  • Effective communication and teamwork skills
  • Basic computer proficiency, including experience with electronic quality systems and Microsoft Office

Benefits

Comp & perks
  • Medical, dental, and vision covered at 100% for you and your family
  • Flex time off
  • Fun, fast-paced, collaborative environment
  • Work on transformational cardiac healthcare technologies
  • Office outings and opportunities to enjoy time inside and outside the office