New · posted Nov 5
Becton Dickinson · Medical Devices
QA Supervisor (2nd Shift)
- El Paso, TX
- On-site
- Full-time
- Manager
The role
The Quality Assurance Supervisor will provide direct management of technical staff. The Quality Assurance Supervisor contributes to the execution of the tactics required to achieve departmental objectives. The Quality Assurance Supervisor is key in assisting the Quality Manager in ensuring product safety, quality and compliance with all relevant global regulations and customer expectations. They will also assist in monitoring frequency and scale of quality and organizational issues and in offering resolutions to these issues
What you need
Education
- Minimum of a bachelor’s degree in Science, Engineering, or other relevant discipline; master’s degree preferred.
Required Skills
Optional Skills
Experience
- Minimum of three (3) years of relevant technical experience in a pharma or medical device manufacturing environment (including project leadership).
- Experience in managing Supplier Audit programs and deployment of corporate initiatives.
- Ability to clearly understand and manage business needs.
- People development skills.
Knowledge and Skills
- Knowledge of managing incoming inspection process for complex parts.
- Knowledge of calibration processes and standards preferred.
- Ability to travel as needed.
What you'll do
- Supervise quality activities and compliance programs within specific focused areas (Supplier Quality, Quality Operations and Project Quality).
- Implement local business organizational goals; specifically around quality.
- Proactively identify and work through obstacles that may hinder associates from focusing on and delivering their individual impact goals.
- Ensure her/his organization is staffed, organized and resourced to fulfill its obligations and to comply with applicable regulations and procedures.
- Supervise/Train / mentor Quality personnel at the Engineering Level.
- Assist Quality Manager to support external/internal audits (FDA, ISO, Segment Audits, Customer Audits, etc.)
- Participate as team members on blitzes, six sigma projects, etc.
- Implement best quality practices.
- Prioritize quality and compliance minded solutions for her/his area of responsibility
- Contributes to the attainment of budget goals by managing department spends
Pay
Becton Dickinson didn't publish pay for this role
See what similar roles pay on Regulatory Jobs, or try the salary calculator.
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.
Where you'll work
El Paso, TXOn-siteOpen in Maps (opens in a new tab)
More jobs in El Paso, TXWorking conditions
- Sitting and work on computer, moderate work on the production floor, moderate walking.
- Manufacturing.
Primary Work Location
USA TX - El Paso - Northwestern Dr.
From the posting
About BD
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.
Equal opportunity, accessibility and legal noticesBecton Dickinson's statements, word for word
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.
Job intelligence
The context around this role
Live data · November 5, 2026
Salary intelligence
How the pay compares
Manager roles in the US60 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $117,125 | $145,250 | $162,750 |
Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, November 5, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 348 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not BD's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 20 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance7
- Collaboration and leadership3
- Quality systems and risk2
- Documentation and SOPs1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Assurance work in medical devices, each linked to the agency or standards body that publishes it.
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices, aligned with ISO 13485
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 14971(official source, opens in a new tab)Application of risk management to medical devices
- FDA21 CFR Part 803(official source, opens in a new tab)Medical device reporting of deaths, serious injuries and malfunctions
- ISOISO 19011(official source, opens in a new tab)Guidelines for auditing management systems
- ISOISO 2859-1(official source, opens in a new tab)Sampling procedures for inspection by attributes (AQL sampling plans)
- HHS-OIGHHS-OIG General Compliance Program Guidance(official source, opens in a new tab)The federal government's guide to healthcare compliance programs and the anti-kickback statute
- ISOISO/IEC 17025(official source, opens in a new tab)Competence of testing and calibration laboratories
- FDA21 CFR Part 806(official source, opens in a new tab)Reports of medical device corrections and removals
- EUEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation: CE marking, technical documentation, vigilance
- FDAMDSAP(official source, opens in a new tab)The Medical Device Single Audit Program shared by five regulators
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- FDA21 CFR Part 830 (UDI)(official source, opens in a new tab)Unique device identification and the GUDID database
- FDAFDA Computer Software Assurance(official source, opens in a new tab)Risk-based assurance for production and quality system software
- FDAFDA Investigations Operations Manual(official source, opens in a new tab)How FDA investigators plan and conduct inspections
- FDA21 CFR Part 807(official source, opens in a new tab)Establishment registration, device listing and premarket notification
Company hiring pulse
BD on Regulatory Jobs
- 100
- Open roles
- 91
- Distinct roles
- 22
- Locations
By discipline
- Quality72 72%
- Regulatory19 19%
- Clinical9 9%
By level
- Senior & Principal48 48%
- Associate & Specialist31 31%
- Manager18 18%
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QA Supervisor (2nd Shift) at BD
Open until filled.