Technical Product Manager - Digital Pathology

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.