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Exact Sciences Logo Exact Sciences · IT - Administration

Lead Quality Assurance Engineer

United States, Madison 112000.00 - 190000.00 USD / Year · Job Posted February 18, 2026
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Job Description

The Lead Quality Assurance Engineer will provide support to various operational teams for a variety of functions. Based on the scope of the assigned area, activities may include process validation, facility validation, test method validation, risk management, change control, exception management, technology transfer, product development, and supplier management. The position will work within defined protocols and procedures and may lead or assist in developing and documenting new procedures and processes. This role will also be responsible for driving harmonization of the Exact Sciences QMS so that all sites meet the same Quality Standards.

Job Responsibility

  • Represent Quality on a variety of projects as assigned
  • Communicate and collaborate with business partners to ensure robust materials, products, processes, and systems and compliance to procedures and specifications
  • Create documentation and records in the Electronic Quality Management System (EQMS)
  • Perform risk assessments and provide risk mitigation strategies
  • Implement processes to monitor product and process performance, compliance, and reliability
  • Implement, conduct, and report on process quality programs using statistical data analysis
  • Review and approve documentation related to Exact Sciences products
  • Conduct periodic reviews of Quality System documentation
  • Generate and distribute Quality metrics as assigned
  • Generate, prepare, and issue data for assigned quality plans
  • Conduct internal and/or supplier audits to drive process standardization and continuous improvement as required by assigned role
  • Conduct root cause analysis and corrective and preventive actions
  • Partner with various teams with timely investigation and resolution of issues to minimize/prevent business disruptions
  • Lead and assist Operations in the generation, execution, and review of process, test method, and facility qualification/validation and process improvement projects
  • Provide Operations support for Investigations, Out-of-Specifications, Nonconformances, Deviations, and material release
  • Escalate issues when intervention or a change is necessary
  • Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork
  • Support and comply with the company’s Quality Management System policies and procedures
  • Regular and reliable attendance
  • Ability to collaborate and work effectively in change and exception management
  • Ability to frequently and accurately communicate with employees and supporting functions in person, via the telephone, or by email
  • Ability to work effectively in a fast-paced, dynamic environment with shifting and competing priorities
  • Ability to comply with any applicable personal protective equipment requirements
  • Ability to travel up to 15% of working time away from work location, may include overnight/weekend travel
  • Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day

Requirements

  • Bachelor’s degree in a Science or technical field
  • or Associate’s degree in Science or technical field and 2 years of relevant experience in lieu of a Bachelor’s degree
  • 5+ years of experience in quality principles and practice including experience in assigned area (Design Control, Supplier Management, Risk Management, etc.)
  • Design Transfer assignments require 8+ years of experience in process validation principles and practice
  • Manufacturing Support assignments require 8+ years of experience in a manufacturing operation environment
  • Demonstrated ability to successfully work within an CFR 820, ISO 13485, ISO 9001, and/or cGMP structured environment
  • Authorization to work in the United States without sponsorship
  • Demonstrated ability to perform the Essential Duties of the position with or without accommodation

Nice to have

  • 4+ years of experience in a biotech or manufacturing environment, preferably in a GMP and/or ISO13485 environment
  • Certified Auditor is a plus (ISO 13485)
  • Demonstrated experience in support of qualification and monitoring programs
  • Practical experience in FDA and ISO regulated environments
  • Experience with electronic product life cycle (PLM) systems such as Agile

What we offer

  • Paid time off (including days for vacation, holidays, volunteering, and personal time)
  • Paid leave for parents and caregivers
  • A retirement savings plan
  • Wellness support
  • Health benefits including medical, prescription drug, dental, and vision coverage
  • Bonus eligibility
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