About you:
The Project Manager is responsible for the execution of development and design transfer projects within the portfolio. This will be done through daily task management and oversight of project controls and KPI management to ensure adherence to project milestones. The individual will work collaboratively with cross-functional teams which requires excellent verbal and written communication skills. This position is an on-site role, and includes team members both on and off-site, working in a fast-paced environment.
What you'll do:
Apply project management principles to develop disruptive technologies including progressing novel concepts through research to commercialization
Spearhead cross-functional teams including industrial design, firmware, software, mechanical, electrical, assay development and service to achieve success in product commercialization
Work with project teams to scope out work needed to achieve aggressive timelines and to escalate budget and resources constraints
Lead project teams by providing clear direction, ensuring alignment with project goals, and managing stakeholder expectations
Maintains hands-on control of the project through a process of regular project reviews, design reviews and audits.
Ensure project visibility through regular technical, management, and progress meetings by working closely with project analyst to maintain KPI tracking
Deliver projects on-time while maintaining mandatory scope by managing resources and risks and tracking project progress on a day to day basis
Develop detailed project documentation including maintaining up to date project schedules, project status reports, issues logs and meeting decisions.
While executing on the project life cycle, provide suggestions to develop process improvements
Develop and execute a risk management plan to actively manage project risks and opportunities. Should risk events be realized, execute on contingency plans as developed with project teams to ensure creative issue resolution
Ensure the project meets expectations for service and manufacturing transfer in terms of design release, procedure readiness, bills of material readiness, etc.
What you need:
Bachelor's or higher degree in Business Administration, Life Sciences, Engineering, or a related field.
5+ years of project management experience in medical devices or similar regulated industry, preferably in a cGMP environment;
Experience with ISO 13485, CLIA, FDA regulations, negotiations, risk management and supply chain management while working in a global environment and being adaptable to change
Excellent communication skills and attention to detail
Strong organizational skills and ability to multitask across projects
Proven ability to collaborate cross-functionally and participate in multi-disciplinary teams
Proficiency in various project management software tools such as Smartsheet, MS Project, JIRA, MIRO or FigJam
What you’ll get:
An opportunity to shape the future of medical diagnostics and make a meaningful impact on global healthcare
A collaborative environment with a high-performing team dedicated to innovation and excellence;
Competitive compensation and benefits package
A platform to showcase your talents and grow professionally in a company that values your contributions.
What excites us
Prior experience in hardware, software and reagent development projects in the diagnostics industry or other regulated industry with a quality mindset
PMP (Project Management Professional) from PMI (Project Management Institute or similar certification or is willing to pursue
Excellent communication skills (written, verbal, formal presentation) at all levels of the organization
Flexible to work long hours as required to meet project deadlines
Scrum / Agile software development methodology
Lean Six Sigma or other process improvement certification
An appreciation of puns!
About Vital
Vital is revolutionizing the landscape of point-of-care diagnostics with our groundbreaking platform, VitalOne, designed to deliver real-time care wherever patients are. We have built a dynamic team of experts across various disciplines including chemistry, software, engineering, and microfluidics to fulfill our mission of making healthcare more accessible and proactive. At Vital, we seek tenacious, bold, and enthusiastic individuals ready to create impactful change in the healthcare industry.
Vital Biosciences Inc. is an equal opportunity employer and values diversity in the workplace. We are therefore happy to accommodate any individual needs in keeping with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act. If you require accommodation in order to participate in our hiring process, please contact us to make your needs known in advance.
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