R&D Manager

Baylis Medical Technologies•Mississauga, ON

3h•Hybrid

About The Position

At Baylis Medical Technologies, we are dedicated to developing innovative medical devices that enhance patient care and improve lives. Our R&D team is at the forefront of designing, testing, and commercializing groundbreaking technologies for minimally invasive procedures. As an R&D Manager, you will lead a team of talented engineers to advance new product development, develop and advance our capabilities, ensure seamless integration from concept to commercialization, and drive impactful innovation in the medical device industry. This role is an opportunity to shape the future of our product portfolio while fostering a high-performance, collaborative culture within the team.

Requirements

Bachelor's or Master’s degree in Biomedical Engineering, Mechanical Engineering, or a related field.
8+ years of experience in engineering or related fields, with a track record of successful product development and project management.
3+ years’ experience leading technical teams, with demonstrated ability to mentor and develop engineering talent, give and receive feedback, and adapt to changing requirements and priorities.
Crisp and clear communication, tailored to the audience and situation.
Strong organizational and cross‑functional collaboration skills, with the ability to align people and priorities outside of the direct team.
Ability to operate with a high degree of autonomy in an inclusive, fast‑paced environment, exercising sound judgment when priorities or requirements change.
Experience in a regulated environment and understanding of design control processes (ISO 13485, FDA, CE requirements).
Ability to travel (~10%) domestically and internationally.

Nice To Haves

Expertise in packaging design and development, including labeling, sterilization and distribution.
Experience in polymer or coating design and development, manufacturing and testing.
Familiarity with regulatory and compliance standards, including ISO 14971, IEC 60601.
Experience with process improvement methodologies such as Lean or Six Sigma.

Responsibilities

Lead and develop teams of technical specialists, growing internal R&D capabilities and ensuring deep expertise is effectively applied across the project portfolio.
Build and evolve core technical competencies within R&D, enabling the organization to take on more complex products and technologies over time.
Provide strategic insights around a portfolio of medical device projects, ensuring they align with business goals and industry regulations.
Support the ongoing manufacturing and lifecycle management of products by ensuring design requirements, regulatory standards, and customer needs are met.
Mentor and develop R&D team members, fostering a culture of innovation, collaboration, and technical excellence.
Collaborate with quality, regulatory, project management, manufacturing, and marketing teams to ensure smooth product development and market success.
Develop and manage resource plans for R&D initiatives, including staffing, budgeting, and prioritization.
Monitor industry trends and emerging technologies to enhance product offerings and maintain a competitive edge.
Ensure compliance with relevant medical device regulations (ISO 13485, FDA, CE) throughout the product lifecycle.
Contribute to intellectual property (IP) development, including invention disclosures and patent applications.
Present project updates, technical insights, and strategic recommendations to senior management.