Quality Control Technician
About The Position
At huMannity Medtec, you don’t just build a career—you help change lives. As a nonprofit medical research and development organization with a nearly 40-year legacy of innovation, we pioneer life‑enhancing technologies for patients with unmet healthcare needs, turning bold ideas into real-world solutions through collaboration across engineering, science, and clinical expertise. Here, curiosity is encouraged, challenges are meaningful, and every project has the potential to make a lasting human impact—because improving lives isn’t just our mission, it’s what we do every day.
Requirements
- High School diploma or equivalent required
- 3+ years of experience in a regulated manufacturing environment (medical device preferred) required. Equivalent combination of education and relevant experience may be considered.
- Experience managing calibration systems and working with third-party calibration vendors required.
- Familiarity with 21 CFR 820 and/or ISO 13485 requirements related to monitoring and measuring equipment required.
- Strong organizational and documentation skills
- Ability to review records for completeness and accuracy
- Effective communication and cross-functional collaboration skills
- Ability to manage multiple priorities and maintain attention to detail
- Ability to follow established procedures and escalate discrepancies appropriately
- Basic problem-solving and coordination skills
Nice To Haves
- Associate degree in Engineering Technology, Quality, Manufacturing, or related technical field preferred
- Experience with inspection tools (calipers, micrometers, height gauges, torque testers, pin gauges, thread gauges, etc.) preferred.
- Understanding of traceability and tolerance requirements preferred.
- Experience with eQMS systems preferred.
- Basic understanding of validated production equipment is a plus.
- Experience working in a medical device or regulated manufacturing environment
- Familiarity with eQMS systems
- Exposure to audit support activities and regulated quality systems
Responsibilities
- Supports quality system compliance activities related to calibration control, manufacturing documentation review, traceability, audit readiness, and regulated quality operations within a medical device manufacturing environment.
- Supports manufacturing operations through equipment calibration coordination, DHR review activities, and product release support to ensure compliance with production and regulatory requirements.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
