New · posted Nov 4
Becton Dickinson · Medical Devices
QC Lab Technician II
- Mebane, NC
- On-site
- Full-time
- Associate & Specialist
The role
As a result of the combination of the BD Biosciences and Diagnostic Solutions business with Waters Corporation (NYSE: WAT), by applying to this role, you will be applying for a position with Waters. Waters is a global leader in life sciences, dedicated to accelerating the benefits of pioneering science through analytical technologies, informatics, and service. With a focus on regulated, high-volume testing environments, Waters’ innovative portfolio harnesses deep scientific expertise across biology, chemistry, and physics. Waters collaborates with analytical laboratories around the world to advance the release of effective, high-quality medicines, assure the safety of food and water, and drive better patient outcomes by detecting diseases earlier, managing routine infections, and combatting growing antibiotic resistance. Through a shared culture of relentless innovation, Waters’ passionate team of approximately 16,000 colleagues partner with customers to turn scientific challenges into breakthroughs that improve lives worldwide.
- Perform visual and analytical testing on incoming, in-process and finished goods, stability samples and product returns for compliance with established quality specifications, including pH, density measurement, spectrophotometry, gas chromatography.
- Perform environmental monitoring for RODI water system and Liquid Media manufacturing.
- Accurately document test results on QC reports, Stability Test reports, Offline Test Requests Validations and First Article Inspections as applicable.
- Analyze data to specifications and designate as accept/reject.
- Work with manufacturing, receiving and materials personnel to complete required QC testing, documentation in a timely manner.
- Perform out-of-specification investigations, troubleshooting, and other duties.
- Prepare standards and control materials. Maintain documentation of preparation.
- Ensure that equipment is cleaned and maintained according to work instructions.
- Maintain inventory to ensure QC lab reagents and supplies are ordered.
- Participate in continuous improvement activities (e.g. kaizen).
- Handle hazardous waste as appropriate.
- Maintain 5S of Quality Labs and Stability Chamber area when used.
- Additional responsibilities as assigned by Quality management.
What you need
- High School Diploma/GED.
- Minimum of 2 years’ experience in current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), or medical device Quality Assurance role. (Associate’s degree in quality, science, or engineering related field may be equivalent to 2 years’ experience), with a minimum of 3 years related laboratory experience.
- Experience with sampling techniques, inspection standards, or use of analytical laboratory equipment.
- Experience working in an FDA regulated environment (medical device or pharmaceutical industry).
- Demonstrated understanding in the use of calibrated equipment and ability to follow equipment maintenance repair procedures.
- Experience with SAP.
- Excellent math skills and the ability to utilize Excel for basic calculations and graphing.
- Must be able to speak, read, and write English fluently as well as write technically and summarize information into data reports using Microsoft Word.
- Excellent attention to detail with a high degree of accuracy and the ability to work independently and in team situations.
- Excellent observation skills with a bias for “corrective action” and improve work environment processes and procedures.
- Demonstrated ability to make critical decisions regarding product quality or quality system compliance.
- Knowledge of basic validation, equipment calibration, equipment maintenance and changing requirements
- Proven capability to prioritize responsibilities and complete tasks on schedule.
Preferred Education / Experience / Skillsnice to have
- Knowledge of statistical techniques used in data analysis programs such as Excel or Minitab.
- Ability to correctly interpret and apply standard sample plans (e.g. American National Standards Institute (ANSI) or Statistical Process Control (SPC) charts) and use designated standards and controls.
Required Skills
Optional Skills
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
Mebane, NCOn-siteOpen in Maps (opens in a new tab)
More jobs in Mebane, NCWorking conditions
- Up to 50% of the workday is spent standing.
- Must be able to work with hazardous chemicals and biohazardous materials in a safe manner.
- Position requires occasional overtime as designated by Operations/Quality management. Overtime duties may be outside of direct area of responsibility.
- 100% on-site work. Schedule may need to flex based on business needs. Position may require nontraditional work weeks such as 5 / 8-hour days.
US BD 1st Shift 8am-430pm (United States of America)
Primary Work Location
USA NC - Mebane
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 4, 2026
Salary intelligence
How the pay compares
Associate & Specialist roles in the US77 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $58,500 | $72,000 | $85,000 |
Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, November 4, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 240 open Quality Control 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 30 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods8
- Documentation and SOPs6
- GMP and compliance5
- Data and digital systems3
- Validation and qualification2
- Quality systems and risk2
- Collaboration and leadership2
- Investigations and CAPA1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Control work in medical devices, led by the two 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
- FDA21 CFR Part 58 (GLP)(official source, opens in a new tab)Good laboratory practice for nonclinical laboratory studiesNamed in the posting
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 2859-1(official source, opens in a new tab)Sampling procedures for inspection by attributes (AQL sampling plans)
- 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 14644-1(official source, opens in a new tab)Cleanroom air cleanliness classification by particle concentration
- ISOISO 11737-1(official source, opens in a new tab)Determination of the microbial population (bioburden) on 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 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- 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
- ISOISO 11607-1(official source, opens in a new tab)Packaging for terminally sterilized medical devices
- ASTMASTM F1980(official source, opens in a new tab)Accelerated aging of sterile barrier systems and medical devices
- ISOISO 11135(official source, opens in a new tab)Ethylene oxide sterilization of health care products
- ISOISO 11137-1(official source, opens in a new tab)Radiation sterilization of health care products
Company hiring pulse
BD on Regulatory Jobs
- 99
- Open roles
- 90
- Distinct roles
- 22
- Locations
By discipline
- Quality72 73%
- Regulatory19 19%
- Clinical8 8%
By level
- Senior & Principal48 48%
- Associate & Specialist32 32%
- Manager16 16%
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QC Lab Technician II at BD
Open until filled.