Quality Assurance Lead

Who We Are

Verily is a subsidiary of Alphabet that is using a data-driven approach to change the way people manage their health and the way healthcare is delivered. Launched from Google X in 2015, our purpose is to bring the promise of precision health to everyone, every day. We are focused on generating and activating data from a variety of sources, including clinical, social, behavioral and the real world, to arrive at the best solutions for a person based on a comprehensive view of the evidence. Our unique expertise and capabilities in technology, data science and healthcare enable the entire healthcare ecosystem to drive better health outcomes.

Description

Verily is seeking an experienced Quality Assurance Lead to join our dynamic Quality and Regulatory Leadership Team. This leadership role will be responsible for managing a team of quality professionals, lead QMS readiness, oversee risk management, along with championing internal and external audits.

Responsibilities

• Partner with internal stakeholders to advise on QMS for software products in development.
• Oversee and lead our current QMS including but not limited to document control, ISO certification, Quality plans, and External Standards.
• Lead and develop a team of QA professionals, fostering a culture of collaboration, innovation, and continuous improvement. Provide guidance, mentorship, and performance feedback to team members.
• Provide oversight of our NCR/ CAPA processes, supplier quality, and design control processes.
• Act as the champion of our internal and external audits, providing leadership and oversight.
  
  

Qualifications

Minimum Qualifications

• Bachelor’s degree in Engineering (e.g., Biomedical, Mechanical, Electrical) or a related field. Advanced degree preferred.
• Minimum of 10 years of experience in Quality Assurance within the medical device industry, including experience with software products and Software as a Medical Device (SaMD).
• Prior experience in managing and developing teams. Strong leadership skills with the ability to inspire and drive a high-performance culture.
• In-depth knowledge of quality systems, nonconformance management, CAPA processes, and document control. Experience with quality-related IT systems and tools. Thorough understanding of FDA regulations, ISO 13485, and other relevant quality standards in the medical device industry.
  
  

Preferred Qualifications

• Ability to adapt to a fast paced start up environment with changing priorities.
• Ability to think strategically, with a strong ability to develop and execute strategies that align with business objectives.
• Excellent communication and interpersonal skills, with the ability to effectively interact with cross-functional teams, senior management, and external stakeholders.
• Strong analytical and problem-solving skills, with a track record of successfully resolving complex quality issues.
  
  

Qualified applicants must not require employer sponsored work authorization now or in the future for employment in the United States.

The US base salary range for this full-time position is $185,000 - $247,000 bonus equity benefits. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus or benefits.