Planet Pharma · 7 hours ago
Sr. Analyst, Project Management
Planet Pharma is seeking a high-energy, detail-oriented Program Manager to lead a critical product transition following a major business unit acquisition. This role involves managing complex projects for the rebranding and modification of medical devices to ensure compliance with new organizational standards.
Responsibilities
Lead Portfolio Transitions: Drive large-scale initiatives focused on relabeling, rebranding, and modifying existing medical devices
Oversee Physical Deliverables: Manage technical updates including molding, tooling changes, and electronics modifications across multiple product lines
Cross-Functional Leadership: Navigate a high-matrix organization, collaborating with Quality, Regulatory, and Manufacturing teams to move products through the Product Cycle Process (PCP)
Project Controls: Use MS Project and related PM systems to maintain timelines and ensure all deliverables meet strict ISO and regulatory standards
Process Compliance: Ensure all project activities align with medical device regulations and internal quality management systems
Qualification
Required
4+ years of project/program management experience, specifically leading complex projects within the medical device industry (or other highly regulated industries)
Proven track record in Manufacturing and R&D program management. Experience with physical products (tooling, molding, hardware) is essential
BA/BS degree required; a degree in an Engineering field is strongly preferred
Deep understanding of ISO standards, Quality systems, and Regulatory requirements
Ability to understand and navigate a large, complex matrix organization
Proficiency in MS Office Suite and MS Project
This is not an IT Project Management role
Preferred
PMP Certification: Preferred
Previous experience working within a large-scale, global corporation
Fluency in Spanish is a plus
Specific experience with rebranding or post-acquisition product integration