Quality Assurance Technician

BD; El Paso (TX); On-site; USD 52,000 - 66,000; Full time

Job summary

BD in El Paso, TX is seeking a Quality Inspector to perform in-process, final, and incoming inspections of medical devices and components to ensure quality and regulatory compliance. You will conduct various tests, document results, and report non-conformances.

The role requires 1–3 years in quality control within regulated industries, strong measurement tool skills, and the ability to work on the 2nd shift. Join a culture that advances health through precise quality work and collaboration.

Qualifications

• Must have a high school diploma or GED; technical associate degree preferred.
• 1–3 years in quality control/assurance, preferably regulated industries like medical devices or pharma.
• Strong understanding of QC principles and methodologies.

Responsibilities

• Perform in-process, final, and incoming inspections of materials, components, and finished devices per procedures and specs.
• Conduct tests including visual, dimensional, functional, and material verification.
• Document results accurately and report non-conformances.
• Initiate NCRs and assist investigations and dispositions of non-conforming materials.
• Use QC tools and equipment (calipers, micrometers, gauges) and support CAPA activities.
• Assist in updating inspection procedures and quality documentation.
• Adhere to GMP, ISO 13485, and FDA 21 CFR Part 820; participate in audits.

Skills

Quality principles

Blueprint reading

Microsoft Office

Detail orientation

Team player

Education

High school diploma or GED

Associate’s degree in a technical field

Tools

Calipers

Micrometers

Gauges

Job description

We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

Job Summary
Responsible for performing quality control inspections and tests on medical devices and components to ensure compliance with quality standards and regulatory requirements.

Job Responsibilities

• Conduct in-process, final, and incoming inspections of materials, components, and finished medical devices according to established procedures and specifications.

• Perform various tests, including visual inspections, dimensional measurements, functional tests, and material verification.

• Document inspection and test results accurately and completely, identifying and reporting non-conformances.

• Initiate Non-Conformance Reports (NCRs) and assist in the investigation and disposition of non-conforming materials.

• Utilize and maintain quality control tools and equipment, including calipers, micrometers, gauges, and other specialized testing apparatus.

• Support root cause analysis and corrective/preventive action (CAPA) activities as needed.

• Assist in the development and revision of inspection procedures and quality documentation.

• Adhere to all safety protocols, Good Manufacturing Practices (GMP), and quality system regulations (e.g., ISO 13485, FDA 21 CFR Part 820).

• Collaborate with production, engineering, and R&D teams to resolve quality issues.

• Participate in internal and external audits as required.

Job Qualifications

• High school diploma or GED required; Associate’s degree in a technical field preferred.

• 1-3 years of experience in a quality control or quality assurance role, preferably within a regulated industry (e.g., medical device, pharmaceutical).

• Strong understanding of quality control principles and methodologies.

• Proficiency in reading and interpreting blueprints, schematics, and technical specifications.

• Experience with various measurement tools and techniques (e.g., calipers, micrometers, gauges).

• Familiarity with Good Manufacturing Practices (GMP) and relevant quality system regulations (e.g., ISO 13485, FDA 21 CFR Part 820) is a plus.

• Excellent attention to detail and strong analytical skills.

• Ability to accurately document and maintain records.

• Basic computer skills, including proficiency with Microsoft Office Suite.

• Good communication and interpersonal skills, with the ability to work effectively in a team environment.

• Ability to lift up to 25 pounds and stand for extended periods.

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visit https://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Required Skills

Optional Skills

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Primary Work Location

USA TX - El Paso - Northwestern Dr.

Additional Locations

Work Shift

US BD 2nd Shift 2pm-10pm (United States of America)