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Becton Dickinson

Global medical devices, lab equipment supplier

Quality Engineering Manager

Biomedical Engineering & Medical Devices +1Confirmed live in the last 24 hours
Full-time$131.6k - $210.5k /yr

About the Job

Requirements

  • A bachelor's degree in Engineering, Science, or a related discipline is required.
  • At least 10 years of progressive experience in Quality Assurance within an FDA-regulated industry is required.
  • At least 3 years of direct management experience of Quality Assurance professional and technical staff is required.
  • Extensive knowledge of applicable regulations and standards, including 21 CFR 820, ISO 13485, ISO 14971, and ISO 10993, is required.
  • A strong understanding of design quality assurance is required.
  • Excellent communication, technical writing, and leadership skills are required.
  • Experience applying Quality Engineering tools, statistics, and problem-solving methodologies is required.
  • Knowledge and skills in Design Control, Change Control, Risk Management and the ISO 14971 process, Process Validation, Design Verification and Design Validation, identification of CTQs, serving as an independent Quality reviewer during Design Reviews, handling deviations and non-conformances, Test Method Validations, Supplier Qualification, Post Market Surveillance and Situation Analysis, CAPA and Root Cause Investigation, and Statistical Analysis are required.
  • Strong strategic planning and prioritization skills and the ability to lead and influence in a matrixed, global organization are required.

Responsibilities

  • Lead the development, sustenance, and continuous improvement of quality systems compliant with 21 CFR 820 and ISO 13485.
  • Execute, measure, and report progress of Quality strategic initiatives.
  • Ensure that policies, procedures, and systems produce products that meet quality and regulatory requirements.
  • Provide Quality Engineering support and promote statistical tools in design and development activities.
  • Lead Risk Management activities in compliance with ISO 14971.
  • Support continuous improvement of quality and market competitiveness.
  • Develop department skills and resources to maintain quality assurance effectiveness.
  • Develop technical solutions to complex quality problems.
  • Lead a team of Quality Engineers at the design center.
  • Perform functional activities with minimal direction.
  • Provide leadership for multidisciplinary projects.
  • Serve as a site and functional Subject Matter Expert for Design Controls.

Desired Qualifications

  • Manufacturing and project management experience is desirable.
  • Knowledge of DFSS and Six Sigma Green Belt or Black Belt is desirable.

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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