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New · posted Oct 19

Becton Dickinson · Medical Devices

Quality Specialist

  • Plainfield, IN
  • On-site
  • Full-time
  • Senior & Principal
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EmploymentFull-time
Deadline

Open until filled

What you need

Minimum Requirement

  • Degree level qualification; or equivalent combination of education and experience.

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.

Required Skills

Optional Skills

What you'll do

  1. Support the development, implementation, and ongoing maintenance of Quality Management System (QMS) processes to ensure full compliance with FDA 21 CFR 820 and ISO 13485 requirements.
  2. May serve as a Regional Site CAPA Lead for the North America region, providing leadership and hands-on support for CAPA activities, including investigation management, root cause analysis (RCA), and development and execution of corrective and preventive action plans.
  3. Provide mentorship and guidance to North America regional teams on QMS requirements, including Nonconformance, Planned Deviations, and Audit processes, while actively contributing to continuous improvement initiatives
  4. Lead and facilitate monthly North America Region Nonconformance Coach meetings to promote consistency, knowledge sharing, and effective issue resolution.
  5. Ensure regional procedures for Nonconformance and Planned Deviations are aligned with global procedures and remain compliant with applicable regulatory and quality system standards.
  6. Support internal and external QMS audits by preparing documentation, participating in audit activities, and driving corrective actions to ensure compliance and continuous improvement.
  7. Analyze quality metrics and trend data to proactively identify risks, systemic issues, and opportunities for quality improvements related to nonconformances and planned deviations.
  8. Own and maintain the integrity of nonconformance records, ensuring completeness, accuracy, traceability, and compliance with regulatory and internal requirements.
  9. Ensure consistent application and adherence to ISO 13485, FDA 21 CFR 820, and Global policies and procedures across all assigned QMS processes.
  10. Build and maintain strong, collaborative working relationships across all organizational levels, supporting and leading Quality Management System activities and cross‑functional projects as needed.
  11. May assist in other duties as required.

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

Plainfield, INOn-siteOpen in Maps (opens in a new tab)

More jobs in Plainfield, IN

Working conditions

Primary Work Location

USA IN - Plainfield

Additional Locations

USA NC - Four Oaks

Well over a hundred smiling BD associates in team shirts gathered outside BD's plant in the Dominican Republic

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.

BD company page · 86 open roles
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 · October 20, 2026

Salary intelligence

How the pay compares

Senior & Principal roles in Indiana14 roles publishing pay

Middle half $117,000 to $132,125, median $119,000

Senior & Principal roles in the US302 roles publishing pay

Middle half $102,625 to $137,500, median $120,250
Annual base pay
Annual base payLowMedianHigh
Indiana$117,000$119,000$132,125
All US$102,625$120,250$137,500

Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 20, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Assurance

The general path across 895 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not BD's own promotion track.

  1. One step back

    Associate & Specialist

    Often: Quality Engineer · Quality Technician

    $81K median243 open
  2. This role

    Senior & Principal

    Often: Quality Engineer · Senior Quality Engineer

    $120K median381 open
  3. Next step

    Manager

    Often: Manager, Quality Assurance · Quality Manager

    $155K median138 open
  4. Later

    Director

    Often: Director, Quality · Associate Director, Quality Assurance

    $209K median118 open
  5. Later

    VP & Executive

    Often: AVP · Executive Director Quality, Cell & Gene Therapy

    $302K median15 open

Skills DNA

What this role leans on

How many of the posting's 15 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 5 linesLab testing and methods: 1 lineDocumentation and SOPs: 4 linesInvestigations and CAPA: 6 linesValidation and qualification: 1 lineQuality systems and risk: 7 linesCollaboration and leadership: 5 linesGMPLab testingDocumentationInvestigationsValidationQuality systemsTeamwork
  • Quality systems and risk7
  • Investigations and CAPA6
  • GMP and compliance5
  • Collaboration and leadership5
  • Documentation and SOPs4
  • Lab testing and methods1
  • Validation and qualification1

Company hiring pulse

BD on Regulatory Jobs

86
Open roles
77
Distinct roles
18
Locations

By discipline

  • Quality68 79%
  • Regulatory16 19%
  • Compliance & Safety2 2%

By level

  • Senior & Principal42 49%
  • Associate & Specialist26 30%
  • Manager15 17%
See all 86 BD roles

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Quality Specialist at BD

Open until filled.

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