Technical Product Manager
Project Duration: 6-12 months
Mississauga, Canada
The Opportunity
- Translate product strategy into detailed scientific requirements for prototype construction and final product development by engineering and data science teams.
- Be the voice of the customer for the product development team throughout the entire product development lifecycle, from definition to sunsetting of the product.
- Collaborate with customers, team members, and outside influencers to ensure a proven and well-rounded understanding of products and developing needs.
- Maintain in-depth knowledge of the digital pathology market, portfolio, and of our competitors.
- Be the high-availability resource for answering questions posed by engineers, data scientists, and designers about stories in the backlog on a day-to-day basis.
- Author user stories, acceptance criteria, product, and software requirements documentation, ensuring that story content and prioritization is aligned to larger strategic goals.
- Support the User acceptance testing activities by interacting with stakeholder/s. Prepare release notes and update the business owners regarding features being incorporated in each Release.
Who you are
- You hold a bachelor degree in Computer Science, Mathematics, Physics, Electrical Engineering or equivalent and have a minimum of 3 years experience in Technical Product Management in the health care service industry OR developing SaMD/Digital Health products OR analogous experience managing requirements of computer vision systems based on AI/ML.
- You have a proven track record with Agile methodologies including Scrum and Scaled Agile Framework.
- You demonstrate Product Management skills - handling priorities, quality, conflict, risk, etc.
Preferred
- You have an advanced degree in Bioinformatics, Computational Sciences, Data Science, Biology, Chemistry or equivalent.
- You demonstrate proven understanding of the digital pathology space and the associated technologies.
- You have experience in regulated industries, specifically Medical Devices/Digital Health/Lifesciences.
- You demonstrate an understanding of US FDA regulations and guidelines.
- Occasional travel may be required in the amount of 10-20% for conferences and client visits.
