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Becton Dickinson

Global medical devices, lab equipment supplier

Quality Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A degree-level qualification or an equivalent combination of education and experience.

Responsibilities

  • Support the development, implementation, and ongoing maintenance of Quality Management System processes to ensure full compliance with FDA 21 CFR 820 and ISO 13485 requirements.
  • 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, and development and execution of corrective and preventive action plans.
  • Provide mentorship and guidance to North America regional teams on Quality Management System requirements, including Nonconformance, Planned Deviations, and Audit processes, while actively contributing to continuous improvement initiatives.
  • Lead and facilitate monthly North America Region Nonconformance Coach meetings to promote consistency, knowledge sharing, and effective issue resolution.
  • Ensure regional procedures for Nonconformance and Planned Deviations are aligned with global procedures and remain compliant with applicable regulatory and quality system standards.
  • Support internal and external Quality Management System audits by preparing documentation, participating in audit activities, and driving corrective actions to ensure compliance and continuous improvement.
  • Analyze quality metrics and trend data to proactively identify risks, systemic issues, and opportunities for quality improvements related to nonconformances and planned deviations.
  • Own and maintain the integrity of nonconformance records, ensuring completeness, accuracy, traceability, and compliance with regulatory and internal requirements.
  • Ensure consistent application and adherence to ISO 13485, FDA 21 CFR 820, and global policies and procedures across all assigned Quality Management System processes.
  • Build and maintain collaborative working relationships across all organizational levels, supporting and leading Quality Management System activities and cross-functional projects as needed.
  • Assist with other duties as required.

About the Company

Becton Dickinson

Global medical devices, lab equipment supplier

BD (Becton, Dickinson and Company) is a global medical technology company that designs, manufactures, and sells medical devices, laboratory equipment, and related services for hospitals, labs, clinicians, and biopharma partners. It operates in four segments: Medical Essentials (medication delivery and specimen management devices), Connected Care (medication management and advanced patient monitoring systems), BioPharma Systems (drug delivery systems for pharmaceutical partners), and Interventional (surgical, endovascular, urological, and critical care products). In addition to devices, BD offers connected software, analytics, clinical education, customer portals, and service programs to support its products. The company’s goal is to help healthcare providers improve patient outcomes by enabling safer and more efficient delivery of care through integrated devices, data, and services across the health ecosystem.

Company size
10,001+
Company stage
IPO
Headquarters
Franklin Lakes, NJ
Founded
1961

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