Description

You will manage complex projects within a regulated medical device environment.

This role is on-site.

Responsibilities

• Manage full project lifecycles for medical devices or similar regulated industries.
• Oversee risk management and supply chain activities in a global setting.
• Conduct negotiations and ensure strict compliance with industry regulations.
• Adapt project plans to accommodate changing requirements and constraints.

Required Skills

• 5+ years of project management experience in regulated industries.
• Proficiency with Smartsheet, MS Project, Jira, and Miro.
• Experience with ISO 13485, CLIA, and FDA regulations.
• Background in hardware, software, or reagent development projects.
• Familiarity with Scrum or Agile software development methodology.
• Demonstrated experience in risk management and supply chain management.
• Bachelor's degree in Business Administration, Life Sciences, Engineering, or related field.

Key Skills

Education

Bachelor's degree