What are the responsibilities and job description for the Medical Device Quality Assurance Manager position at Verily Life Sciences?
Verily Life Sciences Overview
Verily is a subsidiary of Alphabet, utilizing a data-driven approach to revolutionize the way people manage their health and healthcare delivery. Founded in 2015, our mission is to bring precision health to everyone, every day.
We combine expertise in technology, data science, and healthcare to empower the entire healthcare ecosystem to achieve better health outcomes.
Job Description:
As an experienced Quality Assurance Lead, you will join our dynamic Quality and Regulatory Leadership Team. This leadership role involves managing a team of quality professionals, overseeing QMS readiness, risk management, and championing internal and external audits.
You will partner with internal stakeholders to advise on QMS for software products in development, oversee and lead our current QMS, including document control, ISO certification, Quality plans, and External Standards.
The ideal candidate will have a Bachelor's degree in Engineering (e.g., Biomedical, Mechanical, Electrical) or a related field, with at least 10 years of experience in Quality Assurance within the medical device industry, including experience with software products and Software as a Medical Device (SaMD).
Key qualifications include strong leadership skills, in-depth knowledge of quality systems, nonconformance management, CAPA processes, and document control, as well as experience with quality-related IT systems and tools.
Verily is a subsidiary of Alphabet, utilizing a data-driven approach to revolutionize the way people manage their health and healthcare delivery. Founded in 2015, our mission is to bring precision health to everyone, every day.
We combine expertise in technology, data science, and healthcare to empower the entire healthcare ecosystem to achieve better health outcomes.
Job Description:
As an experienced Quality Assurance Lead, you will join our dynamic Quality and Regulatory Leadership Team. This leadership role involves managing a team of quality professionals, overseeing QMS readiness, risk management, and championing internal and external audits.
You will partner with internal stakeholders to advise on QMS for software products in development, oversee and lead our current QMS, including document control, ISO certification, Quality plans, and External Standards.
The ideal candidate will have a Bachelor's degree in Engineering (e.g., Biomedical, Mechanical, Electrical) or a related field, with at least 10 years of experience in Quality Assurance within the medical device industry, including experience with software products and Software as a Medical Device (SaMD).
Key qualifications include strong leadership skills, in-depth knowledge of quality systems, nonconformance management, CAPA processes, and document control, as well as experience with quality-related IT systems and tools.
