A major medical device company in Irvine, CA is in immediate need of a Program Manager consultant for at least 6 months (potential extension for additional 6 months). This is a fully onsite position.
This consultant will support the Senior Director of Program Management and cross-functional teams to support material changes, product redesign efforts, and other areas as needed.
Responsibilities :
- Lead and manage cross-functional projects related to product development, quality improvement, or process optimization.
- Develop project plans, timelines, resource allocations, and risk management strategies.
- Track and report project / program status, deliverables, budgets, and milestones to stakeholders and senior leadership.
- Facilitate effective communication between departments.
- Ensure project documentation meets internal standards and complies with relevant regulatory requirements (e.g., FDA 21 CFR Part 820, EU MDR).
Top Requirements :
Bachelor’s degree in Engineering, Life Sciences, or related field.5+ years of project and program management experience, with at least 2 years in the medical device industry.Strong knowledge of medical device regulations, including FDA and ISO 13485.Proven ability to manage complex projects with multiple stakeholders and deliver results on time and within budget.Excellent organizational, communication, and interpersonal skills.Proficiency with project management and collaboration tools.