Required:
A Bachelor’s degree
6+ years’ experience in Engineering program or project management associated with product development in a medical device or a regulated industry
Experience in more than one of the following disciplines: New Product Development, R&D Engineering, Manufacturing
Experience leading projects from initial concept, through development and verification/validation testing, and into Manufacturing. Ability to balance customer, manufacturing, business and regulatory requirements to expedite launch of the right product to market.
Demonstrated proficiency in program management tools and procedures for setting and tracking performance, quality, time and cost; strong planning and organization skills required.
Preferred:
Strong project/program management skills, including planning, tracking performance, quality, timelines and costs; PMP a plus.
Proven leadership abilities in conflict resolution, negotiation, and driving results.
Effective at leading and collaborating in a matrixed, cross‑functional environment (e.g., Legal, Regulatory, Operations, Procurement, Clinical, Marketing, Quality).
Excellent interpersonal and influence skills with experience managing multidisciplinary teams.
High attention to detail with strong follow‑through to proactively identify and prevent issues.
Excellent communication (written, verbal and executive presentation) skills.
Successful track record managing projects through the medical device PDP process, delivering on schedule and budget.
Strong analytical skills and ability to make data-driven decisions across functional areas.
Interest in applying AI tools to automate or enhance project management tasks.
