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Hologic

Develops medical devices for early detection

Lead Design Assurance Engineer

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeIn-person

About the Job

Requirements

  • In-depth understanding of medical device regulations and standards, including ISO 13485, ISO 14971, IEC 62366, IEC 60601, 21 CFR Part 820, MDD 93/42/EEC, EU MDR, and MDSAP.
  • Familiarity with reliability modeling and testing for electro-mechanical devices and capital equipment.
  • Expertise in design inputs and requirements analysis, design verification and validation, and design transfer processes.
  • Advanced knowledge of risk management principles, including hazard analysis and Failure Mode and Effects Analysis (Design, Usability, and Process).
  • Thorough understanding of test method validation, statistical methods, and failure investigations and root cause analysis.
  • Ability to lead design assurance efforts across the product lifecycle, from concept to launch and post-market activities.
  • Ability to identify gaps, assess risk, and implement corrective actions.
  • Project management skills, including prioritization, planning, and timely execution of critical tasks.
  • Ability to communicate and collaborate with cross-functional teams to ensure alignment on design and compliance goals.
  • Ability to critically assess and advocate for compliance in written product and project documentation.
  • Leadership and mentoring skills to guide junior engineers and foster a culture of quality and innovation.
  • Familiarity with continuous improvement practices and strategies to optimize processes and enhance product quality.
  • A Bachelor of Science degree in a related engineering discipline is required.
  • At least 8 years of medical device industry experience with a Bachelor’s degree in a related engineering discipline, or at least 5 years of experience with a Master’s degree.
  • Proven track record in design assurance activities, including verification and validation, risk management, and regulatory compliance.
  • Demonstrated expertise in test method validation, statistical analysis, and root cause failure investigations.

Responsibilities

  • Lead design assurance activities in new product development, maintaining design controls, risk management, and global regulatory compliance from concept through product launch.
  • Work cross-functionally to define design requirements.
  • Oversee verification and validation processes.
  • Champion continuous improvement initiatives.
  • Drive design assurance efforts across the product lifecycle, including post-market activities.
  • Guide junior engineers and foster quality and innovation.
  • Take responsibility for deliverables and ensure adherence to regulatory and quality standards.
  • Assess gaps and risks and implement corrective actions.
  • Prioritize and plan critical tasks and execute them on time.
  • Assess and advocate for compliance in written product and project documentation.
  • Drive initiatives to optimize product development and design assurance performance.

Desired Qualifications

  • A Master’s degree in a related engineering discipline is preferred.
  • Hands-on experience with electro-mechanical devices and capital equipment.

About the Company

Hologic

Develops medical devices for early detection

Hologic develops medical devices and diagnostic products for breast health, skeletal health, diagnostics, GYN surgery, and medical aesthetics. Its tests and imaging devices help hospitals and labs screen, diagnose, and guide treatment, while surgical and aesthetic tools support procedures. Revenue comes from product sales and related services. The company aims to improve health by enabling early detection and effective treatment worldwide.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Santa Clara, CA
Founded
1985

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