Director of Central Engineering

3 weeks ago

Burnaby, British Columbia, Canada Verathon Full time

Job Summary

Verathon is seeking a highly skilled Director of Central Engineering to lead our Visualization Business Unit R&D Team in Burnaby, BC. This critical role involves overseeing Systems and Human Factors Engineering, Verification Engineering, and Sustaining teams from product conceptualization to commercialization, ensuring innovative and high-quality medical devices are brought to market.

Key Responsibilities

  • Develop and implement R&D strategies aligned with organizational goals, market trends, and technological advancements in the medical device industry.
  • Lead support for multiple R&D projects simultaneously, establishing timelines, milestones, and resource allocation to ensure on-time delivery and budget adherence.
  • Oversee product requirement, risk analysis and mitigation (FMEAs), and Verification and Validation testing of medical devices, ensuring compliance with regulatory standards, such as FDA regulations and ISO requirements.
  • Foster a culture of innovation within the R&D team, encouraging creativity, idea generation, and exploration of novel technologies and process improvements to address unmet clinical needs and improve patient outcomes.
  • Collaborate closely with other departments, including regulatory affairs, quality assurance, manufacturing, and marketing to integrate diverse perspectives and ensure seamless product development and commercialization processes.
  • Identify and mitigate technical, regulatory, and business risks associated with R&D projects, employing proactive risk management strategies to minimize project delays and ensure product safety and efficacy.
  • Stay abreast of regulatory requirements and industry standards for medical devices, ensuring that all R&D activities and product designs adhere to applicable regulations and guidelines.
  • Recruit, mentor, and develop R&D team members, fostering a culture of continuous learning, professional growth, and knowledge sharing within the department.
  • Manage R&D budgets and resources effectively, optimizing investments to maximize ROI while maintaining high-quality standards and project deliverables.

Requirements

  • Bachelor's degree in engineering, biomedical engineering, or related field; advanced degree (MS, PhD) preferred.
  • Proven experience (8+ years) in R&D leadership roles within the medical device industry, with a track record of successfully bringing innovative products to market.
  • In-depth knowledge of medical device regulations and quality standards (FDA 510(k), ISO 13485), with experience navigating regulatory pathways and obtaining regulatory approvals.
  • Strong management skills, including the ability to prioritize tasks, manage multiple projects simultaneously, and deliver results on schedule and within budget.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and communicate complex technical concepts to non-technical stakeholders.
  • Strategic thinking and problem-solving abilities, with a focus on driving innovation, mitigating risks, and achieving business objectives.
  • Leadership qualities, including the ability to inspire and motivate team members, foster a culture of innovation and excellence, and lead by example.
  • Analytical mindset, with the ability to analyze market data, interpret trends, and make data-driven decisions to inform R&D strategies and product development priorities.

Compensation

Salary range – $152,500-229,800 (Compensation will vary based on skills, experience, and location. If this position is filled outside the Greater Vancouver, BC area, this salary range will vary depending on the specific hiring location.)

Full-time non-sales employees are eligible for Verathon's annual bonus plan based on company and individual performance.

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