Quality Assurance - GMP at TotalMed Medfi
Holly Springs, NC 27540, USA -
Full Time


Start Date

Immediate

Expiry Date

20 Nov, 25

Salary

29.0

Posted On

20 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Continuous Improvement, Analytical Skills, Iso, Communication Skills, Teams

Industry

Information Technology/IT

Description

JOB SUMMARY

We are seeking a detail-oriented and proactive Quality Assurance Analyst to join our team. The ideal candidate will play a crucial role in ensuring the quality and reliability of our products through rigorous testing and inspection processes. This position involves analyzing data, conducting quality audits, and maintaining compliance with industry standards such as ISO 9001 and ISO 13485. The Quality Assurance Analyst will work closely with various departments to coordinate quality assurance activities and support continuous improvement initiatives.

EXPERIENCE

  • Proven experience in quality assurance or a related field is preferred.
  • Familiarity with quality inspection techniques and tools, including Calypso software for measurement analysis.
  • Strong analytical skills with the ability to interpret data effectively.
  • Knowledge of ISO 9001 and ISO 13485 standards is highly desirable.
  • Excellent attention to detail and problem-solving abilities.
  • Strong communication skills, both written and verbal, for effective collaboration across teams.
    Join us in our commitment to delivering high-quality products while fostering a culture of continuous improvement!
Responsibilities
  • Analyze product specifications and requirements to ensure compliance with quality standards.
  • Conduct quality inspections throughout the manufacturing process to identify defects or deviations from specifications.
  • Utilize Coordinate Measuring Machines (CMM) for precise measurements and data collection.
  • Fabricate test samples as needed for quality testing purposes.
  • Perform regular quality audits to assess adherence to ISO 9001 and ISO 13485 standards.
  • Document findings, prepare reports, and communicate results to relevant stakeholders.
  • Collaborate with engineering and production teams to implement corrective actions for identified issues.
  • Maintain accurate records of inspections, tests, and audit results in accordance with company policies.
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