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Hologic

Develops medical devices for early detection

Clinical QA Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeIn-person

About the Job

Requirements

  • Comprehensive understanding of FDA Quality System Regulations, ISO 13485, EU Medical Device Regulation, and ISO 14971 for risk management.
  • Strong knowledge of medical procedures and the expected and potential outcomes related to Hologic’s product portfolio.
  • Familiarity with post-market surveillance requirements, adverse event reporting, and health risk assessments.
  • Awareness of regulatory reporting processes, including MedWatch reports, notified body communications, and external notifications.
  • Ability to independently collect, analyze, and assess information associated with adverse events and determine appropriate next steps.
  • Ability to communicate with internal teams, sales personnel, customers, patients, and regulatory agencies.
  • Organizational skills to ensure timely documentation, reporting, and follow-up of adverse events and regulatory submissions.
  • Analytical skills to support and lead investigations, including corrective and preventive actions (CAPAs), nonconformances, and other quality system processes.
  • Experience developing metrics and quality reports related to reportable events and identifying potential excursions.
  • Ability to improve processes to enhance efficiency and compliance with post-market surveillance requirements.
  • Proficiency in leading or participating in internal and external audits, inspections, and assessments.
  • Bachelor’s degree in Medicine, Nursing, Biomedical Engineering, Electromedical Engineering, or a related field; Risk Managers will also be considered.
  • At least 5 years of experience in a similar role, preferably within the medical device or healthcare industry.
  • Hands-on experience with adverse event reporting, regulatory communications, and health risk assessments.
  • Track record supporting or leading CAPAs, nonconformances, and quality investigations.

Responsibilities

  • Investigate and report potential and actual adverse events, along with other regulatory reporting activities.
  • Collaborate with Technical Service, Marketing, Sales, and Regulatory teams to ensure timely and thorough documentation, analysis, and reporting.
  • Collect, analyze, and assess adverse-event information and determine appropriate next steps.
  • Support and lead investigations, including CAPAs, nonconformances, and other quality-system processes.
  • Develop metrics and quality reports related to reportable events and identify potential excursions.
  • Lead or participate in internal and external audits, inspections, and assessments.
  • Improve processes to enhance efficiency and compliance with post-market surveillance requirements.

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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