Hologic

Vice President, Quality Engineering - BSH Division

Hologic$237K — $422K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • In-depth knowledge of FDA Quality System Regulations and ISO 13485.
  • Comprehensive understanding of quality assurance and control systems.
  • Familiarity with industry trends and regulatory authority engagement.
  • 14+ years in technical roles within the medical device sector focusing on Quality and R&D.
  • 6+ years in personnel management, with experience overseeing other leaders.

Responsibilities

  • Develop and execute quality strategies for the Breast and Skeletal Health Division.
  • Ensure product compliance with safety, reliability, and durability standards.
  • Partner with divisional leadership to meet organizational goals.
  • Provide technical expertise across cross-functional initiatives.
  • Champion continuous improvement and drive innovation in quality management.

Benefits

  • Opportunity to lead one of the largest divisions at Hologic Inc.
  • Engagement with senior leadership teams on strategic decisions.
  • Access to a collaborative and innovative work culture.
  • Opportunities for talent management and employee development.
  • Involvement in cutting-edge developments in medical device quality.
Full Job Description
Job Description

The Vice President of Quality for the Breast and Skeletal Health Division is a pivotal executive leadership role responsible for developing and executing quality strategies across one of the largest divisions at Hologic Inc.

This position ensures that all products meet the highest standards of safety, reliability, durability, and performance while maintaining compliance with regulatory requirements throughout the full product lifecycle-from new product development to post-market surveillance and product lifecycle management. As a member of both the Divisional Senior Leadership Team and the Global Quality Leadership Team, you will partner with divisional leadership to drive organizational goals, provide technical expertise, and influence cross-functional initiatives at the highest levels.

Knowledge
  • In-depth understanding of FDA Quality System Regulations, ISO 13485, Medical Device Directive, Medical Device Regulation, risk management, and cybersecurity management.
  • Comprehensive knowledge of technical quality assurance and control systems, including standards, methods, and procedures for product inspection, testing, and evaluation.
  • Awareness of industry trends through review of technical publications and active engagement with regulatory authorities.

Skills
  • Demonstrated ability to lead and inspire senior leaders, including Directors, and manage large global teams.
  • Strong analytical and problem-solving skills at both managerial and technical levels.
  • Excellent written and oral communication skills, with the capacity to influence and present to regulatory bodies, technical functions, customers, field teams, and executive leadership up to the CEO.
  • Expertise in change management, independent decision-making, and conflict resolution.
  • Proficiency in hosting and managing third-party audits (e.g., FDA, notified bodies) and responding to regulatory findings.

Behaviors
  • Champion innovation and continuous improvement by capturing and communicating lessons learned and driving the adoption of new tools, technologies, and methods.
  • Excel in talent management, including attracting, hiring, developing, and retaining top talent, as well as managing succession planning and employee development.
  • Lead by example through objective setting, performance management, regular feedback, and recognition.
  • Promote a culture of quality and compliance while fostering cross-functional collaboration and stakeholder engagement.

Experience
  • Minimum of 14 years' experience in technical roles within the medical device industry, with a focus on Quality and R&D.
  • At least 6 years in a personnel management role, including experience managing other people leaders.
  • Proven track record in product launch excellence, post-market quality management, and leading quality activities related to mergers and acquisitions.
  • Experience in developing, implementing, and maintaining Quality Management Systems to support regulatory and certification requirements.

The annualized base salary range for this role is $237,600 - $422,400 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.

Agency and Third-Party Recruiter Notice

Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.

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About Hologic

Hologic, Inc. is an American medical technology company that develops and manufactures diagnostic products, medical imaging systems, and surgical products. The company's products are used in a wide range of medical applications, including breast cancer screening, cervical cancer screening, and osteoporosis diagnosis. Hologic is headquartered in Marlborough, Massachusetts, and has operations in North America, Europe, and Asia. The company was founded in 1985 and has grown to become one of the largest medical technology companies in the world.
Learn more about Hologic
Size
6,705 employees
Market Cap
$18.5 billion
Industry
Net Income
$1.3 billion
Founded
1985
5 Year Trend
+9.7%
Revenue
$4.5 billion
NASDAQ

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