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Strong fit if you like structured quality work—testing, inspection, equipment care, and precise paperwork—in a medical-technology manufacturing context at an on-site base location.
As a Quality Coordinator at Nissha Medical Technologies, a typical day centers on product and process quality checks: running routine and non-routine analyses on materials or finished goods, comparing results to specs and control limits, and recommending release readiness. You also support equipment readiness (calibrate, validate, maintain), keep lab cleanliness and safety standards, do visual inspections, and complete testing documentation such as data forms, logbooks, and inventory records.
Build strength in lab and in-process testing, specs vs. control-limit interpretation, equipment calibration/validation, visual inspection, and clean, complete quality records. No certification list was provided for this posting.
No. The listing marks remote as off; work is tied to Peterson Air Force Base, El Paso County.
Analyses of materials and products, interpreting results against specs, equipment upkeep, inspections, and supporting documentation.
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Quality Coordinator at Nissha Medical Technologies - Peterson Air Force Base, El Paso County Role Overview The Quality Coordinator plays a crucial role in ensuring that all quality standards and regulatory requirements are met within Nissha Medical Technologies. This full-time position is based at the Peterson Air Force Base location. Your Responsibilities Conduct inspections of production areas to ensure compliance with quality standards and regulations. Develop, implement, and maintain quality control procedures for all products manufactured by NMT. Review and approve product specifications and documentation to ensure they meet regulatory requirements. Collaborate with cross-functional teams to identify and resolve quality issues. Maintain records of quality audits and inspections for internal and external review. Skills & Qualifications Bachelor's degree in Quality Management, Industrial Engineering, or a related field is required. A Master’s degree is preferred. Certified Quality Engineer (CQE) or similar certification is highly desirable. Minimum of 3 years of experience in the medical device industry, with at least 2 years in quality assurance/quality control roles. Familiarity with FDA regulations and other relevant international standards such as ISO 13485. Strong organizational skills and ability to manage multiple tasks simultaneously. Excellent communication and interpersonal skills for working effectively with cross-functional teams. Working at Nissha Medical Technologies Nissha Medical Technologies is a global Contract Development and Manufacturing Organization (CDMO) that brings together people, purpose, and technology to advance healthcare. As part of the team, you will work in a dynamic environment where innovation meets precision. Apply Today To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.
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