Medical Device Quality Control Jobs in Texas (NOW HIRING)

Position Description: Job Title: Medical Device Quality & Compliance Specialist (Role: QA/QC) Department: QA/RA Reports To: Nvision Director, Quality & Regulatory Affairs FLSA Status: Exempt Last Modified: 07/16/2026 Summary The Medical Device Quality & Compliance Specialist reports directly to the Directory of Quality and Regulatory Compliance. The Medical Device Quality & Compliance Specialist is responsible for inspecting and verifying product quality throughout all stages of the product development process, including concept through final inspection. This position ensures that materials, components, and finished products comply with engineering drawings, customer specifications, dimensional tolerances, and NVISION quality standards while helping prevent nonconforming products from reaching the customer. Responsibilities include: Interpret and review design drawings, specifications, and other technical documents for project related QAQC requirements/criteria. Conduct dimensional inspections using, calipers (vernier), and other precision measuring equipment with approved product drawings for compliance. Inspect components and finished devices delivered for quantity, quality, and condition and report on missing and/or damaged items. Conduct quality assurance inspections and audits, reporting any non-conformance issues and documenting as observations. Maintain material identification and product traceability throughout production. Identify, document, and report nonconforming materials and products, Stop or contain nonconforming products until disposition is determined. Ensure measuring equipment is properly maintained and removed from service if damaged or out of calibration. Work closely with Engineering, and Management to resolve quality issues. Follow all company safety policies, quality procedures, and manufacturing standards. Maintain inspection records and quality documentation in accordance with company procedures. Assist in maintaining compliance with FDA 21 CFR 820, 21 CFR 1271, and AATB. Participate as member of product development team to understand project specifications, goals, and timelines in preparatory phase and coordination meetings to understand methods for compliance with specifications and industry best practices. Coordinate with various stakeholders, including engineering, fulfillment/operations on discrepancies between drawings, and components or devices. Ensure that all relevant DHF/DMR documents are available on-site for reference. Work closely with project teams to resolve issues that may impact quality and integrity of finished devices. Maintain clear and open communication by providing regular updates on progress, challenges, and resolutions between the suppliers and management. Skills and Qualifications: In-depth knowledge of FDA FDA 21 CFR 820, 21 CFR 1271 regulations and ISO 13485, ISO 14971 & AATB standards for HCTP, Class I, & Class II medical devices Working knowledge of measurement instruments Experience with Good Documentation Practice, document control and record keeping Strong attention to detail and analytical skills Excellent written and verbal communication skills Ability to read, analyze and interpret national and international regulations and quality standards. Some college with 1+ yrs in a similar related role. High school diploma with 4+ yrs in similar related role. Strong working knowledge of the following software programs: Microsoft Word, Excel, Outlook. Ability to multi-task, be detail oriented, prioritize, good oral and written communication. Must be able to demonstrate experience utilizing critical judgement and analytical skills. Preferred- Bachelor's Degree with an interest in Quality Assurance and Quality Control for Medical Devices. Preferred- one year or more of QA/QC experience in Medical Device industry. Preferred- have working knowledge of regulations and standards for medical devices. Capable of lifting 50 pounds. Schedule: 8 hour shift Day Shift Monday thru Friday
$54,000.00 - $60,000.00 Annually