Sr. Project Manager #260006

About the Role

We are seeking a Project Manager – Product Development to lead end-to-end medical device initiatives from concept through commercialization. In this role, you will champion modern project management methodologies (such as Agile and iterative frameworks), guide cross-functional teams, align innovation pipelines with long-term division strategy, and ensure projects hit critical regulatory, quality, and delivery milestones.

Key Responsibilities

• Portfolio & Strategic Planning: Collaborate across product divisions to build innovation pipelines, align development projects with long-term business goals, and provide strategic updates to senior leadership.
• Execution & Delivery: Build, manage, and monitor detailed project plans, scope, budgets, and timelines; translate overarching division objectives into actionable technical tasks.
• Process Leadership: Serve as a subject matter expert in project management tools and portals, applying iterative and Agile frameworks to keep development cycles on schedule.
• Risk Management & Contingency: Proactively conduct risk assessments, identify drivers of scope creep or cost overruns, and implement targeted mitigation plans.
• Team Leadership & Mentorship: Foster transparent cross-functional alignment, build consensus across functional stakeholders, and coach/mentor junior team members.
• Technical & Regulatory Support: Compile technical justifications and data summaries supporting product claims, and spearhead process and quality improvement initiatives.
• Industry Compliance: Maintain an active understanding of medical device regulations, design controls, and emerging industry innovations.

What You Bring

• Education: Bachelor’s degree in Engineering, Science, or a related technical discipline.
• Certification: Project Management Professional (PMP) certification required.
• Experience:
• Minimum of 4 years of experience within medical devices, pharmaceuticals, dietary supplements, or cosmetics.
• Minimum of 2 years of dedicated project management experience.
• Proven track record taking products through development and launch.
• Technical Acumen:
• In-depth knowledge of Class I and Class II medical device requirements, design controls, risk assessments, and the FDA 510(k) pathway.
• Demonstrated mastery of project management tools, frameworks, and portfolio tracking.

Why Join Us?

• True Hybrid Balance: Enjoy remote flexibility on Mondays and Fridays with collaborative in-office days Tuesday through Thursday.
• High-Impact Work: Lead products that directly improve clinical outcomes and patient care.
• Professional Growth: Direct exposure to division leadership and opportunities to mentor emerging PM talent.