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Becton Dickinson

Global medical devices, lab equipment supplier

Regional Quality Integration Leader

Regulatory & Quality (Life Sciences)Updated on Nov 15
Full-time€105.8k - €161.4k /yr

About the Job

Requirements

  • A bachelor's degree or equivalent experience in a scientific, engineering, or related field is required.
  • A minimum of 8–10 years of experience in Quality Assurance in the medical device or pharmaceutical industry is required, including at least 3–5 years in a leadership or management role.
  • Established background guiding and handling quality system integrations associated with mergers, acquisitions, or substantial organizational shifts is required.
  • Comprehensive understanding of applicable medical device regulations, including ISO 13485, EU MDR, IVDR, and FDA QSR, is required.
  • Solid knowledge of quality management concepts, tools, and approaches, including CAPA, FMEA, and lean manufacturing, is required.
  • Proven capability to guide and impact cross-functional teams within a complex, matrixed organization is required.
  • Fluency in English is required.
  • Willingness to travel regularly throughout the EMEA region, up to 40–50%, is required.

Responsibilities

  • Develop and carry out regional quality integration strategies and plans aligned with global quality objectives and local regulatory frameworks.
  • Guide cross-functional teams through integration of quality management systems, processes, and procedures for newly acquired entities or major business changes within the EMEA region.
  • Conduct gap analyses of existing quality systems against BD standards and applicable regulations, including ISO 13485, MDR, and IVDR, and develop and implement remediation plans.
  • Coordinate harmonization of quality documentation, training programs, and quality metrics across integrated sites.
  • Act as the primary point of contact for quality integration matters with regional business leaders, global quality teams, and regulatory affairs.
  • Ensure effective communication and change management strategies support successful quality integration.
  • Monitor and report on the progress of quality integration initiatives, identifying and mitigating potential risks.
  • Participate in due diligence activities for potential acquisitions from a quality perspective.
  • Provide expert mentorship and support to regional teams on quality integration challenges.
  • Foster a culture of continuous improvement and quality excellence throughout the integration process.

Desired Qualifications

  • A master's degree is preferred.
  • Proficiency in other major European languages, such as German or French, is a significant advantage.

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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