Offer summary
Qualifications:
Bachelor’s degree in engineering or equivalent experience, 3+ years project management experience in medical device or regulated industry, Proficient in MS Office; MS Excel highly preferred, Project Management certification (preferred), Experience with Medical Device Regulations.
Key responsabilities:
- Oversee multiple concurrent projects and align with stakeholders
- Develop comprehensive project plans and objectives
- Drive resource allocation and manage project schedules
- Collaborate with Regulatory Affairs and update on project status
- Enhance the product development process overall