New · posted Nov 6
Becton Dickinson · Medical Devices
Quality Control Inspector II
- Tempe, AZ
- On-site
- Full-time
- Associate & Specialist
The role
The Inspector II, Quality Control is a position that facilitates the physical testing and verification inspection for the QC Laboratory at the site. This position assists the Supervisor in managing the daily workflow and problem-solves deviations in the process and products to ensure consistent quality. This position requires flexibility, attention to detail and the ability to manage in a dynamic work environment.
This job description is intended as a summary of the primary responsibilities of and qualifications for this position. The job description is not intended as inclusive of all duties an individual in this position might be asked to perform or of all qualifications that may be required either now or in the future.
What you need
Two ways to qualify
High school
+ 2–3 years of experience
High school diploma or equivalent plus 2–3 years of relevant experience, including quality control laboratory testing or product testing experience; OR
- or
Associate
+ 1+ year of experience
Technical/Associate degree plus at least 1 year of relevant experience, including quality control laboratory testing or product testing.
Required Qualifications
- Basic knowledge of measurement and inspection equipment.
- Possess technical measuring skills.
- Strong attention to detail and documentation skills.
- Basic computer skills, including Microsoft Office applications.
- Must demonstrate the ability to work as a team player, perform as a self-motivator, communicate effectively, follow written procedures, and perform multiple tasks simultaneously
- Read, write legibly, and understand English
- Must have 20/20 correctable vision
Required Skills
Optional Skills
Preferred Qualificationsnice to have
- Experience with calibration or metrology systems.
- Experience with environmental monitoring or basic microbiology laboratory practices.
- Experience performing receiving or incoming material inspections.
- Experience working within a regulated Quality System.
- Familiarity with GMP/GDP practices.
What you'll do
Job Responsibilities: (Primary Duties, Roles, and/or Authorities)
Perform quality control inspection, testing, environmental/microbiological monitoring, and calibration activities in accordance with approved procedures, specifications, drawings, and work instructions.
- Collect, prepare, inspect, and test samples, materials, and components using applicable laboratory and measurement equipment, including Instrons, microscopes, calipers, micrometers, and gauges.
- Accurately interpret equipment readings and document inspection, testing, monitoring, and calibration results in accordance with good documentation practices.
- Review applicable supplier documentation and appropriately identify and document accepted, rejected, or nonconforming materials.
- Identify and escalate abnormal results, discrepancies, equipment issues, and nonconforming conditions, and support investigations and corrective actions as needed.
- Maintain inspection-ready work areas, equipment, supplies, and records, and support calibration activities and internal or external audits as required.
- Follow applicable safety, regulatory, quality system, and company requirements.
- Perform other duties as assigned.
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
Tempe, AZOn-siteOpen in Maps (opens in a new tab)
More jobs in Tempe, AZWorking conditions
- Ability to sit, stand, and walk for extended periods and occasionally bend, reach, stoop, or kneel.
- Ability to handle, inspect, manipulate, and measure small components and samples using inspection and laboratory equipment.
- Ability to perform detailed visual inspections, including distinguishing small defects, markings, contamination, colors, and visual indicators.
- Ability to lift, carry, push, or pull up to 25 pounds, with or without reasonable accommodation.
- Ability to wear required PPE and perform computer-based documentation and data entry throughout the workday
- Work is performed across open cubicle, laboratory, cleanroom, manufacturing, inspection, and warehouse environments.
- Requires compliance with applicable safety, gowning, contamination-control, and PPE requirements.
- May involve exposure to manufacturing equipment, production-floor noise, cleaning agents, laboratory chemicals, and microbiological samples.
- Requires effective collaboration across functions and the ability to work independently in a fast-paced environment.
- Occasional schedule flexibility may be required to support Quality and operational needs.
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
Primary Work Location
USA AZ - Tempe Headquarters
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
BD is an affirmative action, equal opportunity employer that values and actively seeks diversity in the workforce.
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 6, 2026
Salary intelligence
How the pay compares
Associate & Specialist roles in the US53 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $46,000 | $48,000 | $51,500 |
Comparisons: the base pay employers published on open Quality Inspection roles at the same level on Regulatory Jobs, November 6, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Inspection
The general path across 98 open Quality Inspection 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 25 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance7
- Lab testing and methods7
- Documentation and SOPs6
- Investigations and CAPA3
- Quality systems and risk3
- Data and digital systems1
- Collaboration and leadership1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Inspection work in medical devices, led by the one this posting names, 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 13485Named in the posting
- ISOISO 2859-1(official source, opens in a new tab)Sampling procedures for inspection by attributes (AQL sampling plans)
- 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
- ISOISO/IEC 17025(official source, opens in a new tab)Competence of testing and calibration laboratories
- ISOISO 11737-1(official source, opens in a new tab)Determination of the microbial population (bioburden) on medical devices
- ISOISO 14644-1(official source, opens in a new tab)Cleanroom air cleanliness classification by particle concentration
- ISOISO 19011(official source, opens in a new tab)Guidelines for auditing management systems
- ISOISO 11607-1(official source, opens in a new tab)Packaging for terminally sterilized medical devices
- ISOISO 10993-1(official source, opens in a new tab)Biological evaluation of medical devices within a risk management process
- FDA21 CFR Part 803(official source, opens in a new tab)Medical device reporting of deaths, serious injuries and malfunctions
- FDA21 CFR Part 806(official source, opens in a new tab)Reports of medical device corrections and removals
- FDA21 CFR Part 830 (UDI)(official source, opens in a new tab)Unique device identification and the GUDID database
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- FDA21 CFR Part 801(official source, opens in a new tab)FDA labeling requirements for medical devices
- ISOISO 15223-1(official source, opens in a new tab)Symbols for medical device labels and labeling
Company hiring pulse
BD on Regulatory Jobs
- 100
- Open roles
- 100
- Distinct roles
- 22
- Locations
By discipline
- Quality74 73%
- Regulatory19 19%
- Clinical8 8%
By level
- Senior & Principal48 48%
- Associate & Specialist32 32%
- Manager18 18%
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Quality Control Inspector II at BD
Open until filled.