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Hologic

Develops medical devices for early detection

Corporate Quality Principal Auditor

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A bachelor's degree in Engineering, Science, or a related technical discipline is required.
  • At least 5 years of experience as a Principal or Lead Auditor in a regulated industry, with current certifications, is required.
  • At least 3 years of experience in Manufacturing, Quality Engineering, R&D, Compliance, Quality Operations, servicing, refurbishing, chemical compliance, clinical studies, or equivalent is required.
  • Strong knowledge of applicable quality and regulatory requirements, including 21 CFR 820 / QMSR, ISO 13485, MDSAP, FDA regulations, ISO 14971, ISO 19011, ISO 14155, EU MDR, EU IVDR, REACH, RoHS, and Conflict Minerals, is required.
  • Proven experience planning, leading, and supporting internal, external, corporate, site, FDA, supplier, acquisition, transfer, and risk-based audits is required.
  • Ability to assess compliance risk, evaluate audit findings, monitor corrective actions, and support effective CAPA, root cause analysis, and systemic quality improvements is required.
  • Experience with process, equipment, design, test method, and software validation activities is required.
  • Strong data analysis and reporting skills, including audit metrics, trend analysis, executive reporting, and annual Compliance Audit reports, are required.
  • Experience maintaining electronic audit systems or eQMS audit functionality is required.
  • Advanced proficiency with SharePoint, Teams, PowerPoint, Word, and Excel is required.
  • Strong project management skills and the ability to coordinate multi-site and cross-functional audit activities are required.
  • Experience supporting FDA inspection readiness, including front-room and back-room activities, is required.
  • Excellent written and verbal communication skills, including the ability to coach, influence, and act as an audit subject matter expert, are required.
  • An active Lead Auditor certification from a recognized accreditation company is required.

Responsibilities

  • Support key elements of the global Quality Audit program.
  • Develop, maintain, and improve audit metrics and processes.
  • Analyze data and prepare executive-level and detailed audit reports.
  • Plan, lead, and perform risk-based corporate compliance audits, special audits, and gap assessments.
  • Support audits related to new acquisitions, product or process transfers, suppliers, and complex manufacturing processes.
  • Identify compliance risks and drive manufacturing and Quality Management System improvements.
  • Support FDA inspections and external audits, including front-room and back-room activities when needed.
  • Act as an audit subject matter expert and coach, guiding teams on audit expectations, execution, and documentation.
  • Partner cross-functionally with Manufacturing, Quality Engineering, R&D, Compliance, Quality Operations, and other teams.
  • Use regulatory trends, audit outcomes, and internal performance data to support risk-based planning and continuous improvement.

Desired Qualifications

  • Additional global regulatory knowledge, awareness of AI-related healthcare regulation, GCP/GLP understanding, and multilingual capability.

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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