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Hologic

Develops medical devices for early detection

Quality Engineer, CAPA Facilitator

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

About the Job

Requirements

  • Technical bachelor's degree or higher is preferred.
  • Three to eight years of experience in the medical device, in vitro diagnostic, or pharmaceutical industry, with increasing responsibility in quality assurance and CAPA systems.
  • Strong working knowledge of QMSR, ISO 13485, and global quality regulations.
  • Ability to lead cross-functional teams and manage multiple workstreams.
  • Technical writing, analytical, and problem-solving skills.
  • Interpersonal and communication skills, including the ability to provide executive-level updates and support regulatory documentation.
  • Ability to present materials to director-level leadership.
  • Understanding of statistics and statistical analysis.

Responsibilities

  • Serve as a subject matter expert for CAPA, including root cause analysis, effectiveness checks, and sustainable corrective actions.
  • Coordinate and facilitate CAPA Review Board meetings and related documentation.
  • Own and improve the divisional CAPA toolbox, including training materials, templates, and reference resources.
  • Monitor CAPA system health, conduct daily reviews for escalations, and coordinate with departments to support adequate resourcing.
  • Provide input into global CAPA process improvements and related training content.
  • Support and model quality values while promoting accountability, compliance, and continuous improvement.
  • Collaborate with junior staff, peers, and cross-functional stakeholders across multiple organizational levels.
  • Assist in developing, implementing, and maintaining quality assurance procedures, processes, and documentation.
  • Identify opportunities to strengthen QMS processes, including inputs to and outputs from CAPAs.
  • Analyze quality data and trends to identify improvement opportunities and systemic risks.
  • Develop and maintain CAPA and quality metrics, dashboards, and reporting tools.
  • Partner with internal suppliers and stakeholders to review CAPA data, monitoring, and performance.
  • Participate in and support internal and external audits, including FDA inspections, as a CAPA and quality systems subject matter expert.
  • Assist with audit preparation, data collection, and communication with functional areas to support audit readiness and efficiency.
  • Help ensure compliance with applicable FDA regulations, QMSR, ISO 13485, and other relevant global quality standards.
  • Mentor and coach junior team members in CAPA and quality system fundamentals.
  • Provide consultation and training on CAPA principles, methodologies, and best practices to QMS and cross-functional teams.
  • Lead or contribute to CAPA-related remediation projects and continuous improvement initiatives.
  • Support data analysis activities to develop key performance indicators across functions.
  • Review open Quality Plans and provide recommendations for updates or improvements.

Desired Qualifications

  • Experience with Agile or an equivalent Product Lifecycle Management system.

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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