REQUIREMENTS & OVERVIEW:

• Bachelor’s &/or higher degree in Business Administration, Life Sciences, Engineering, or a related field.
• 5+ years of project management experience in medical devices &/or similar regulated industry.
• Experience with ISO 13485, CLIA, FDA regulations, negotiations, risk management & supply chain management while working in a global environment & being adaptable to change.
• Proficiency in various project management software tools such as Smartsheet, MS Project, JIRA, MIRO, Etc.
• Prior experience in hardware, software and reagent development projects in the diagnostics industry or other regulated industry with a quality mindset.
• PMP (Project Management Professional) from PMI (Project Management Institute or similar certification or is willing to pursue.
• Scrum / Agile software development methodology.
• Lean Six Sigma or other process improvement certification.
  *
  Job Types: Full-time, Permanent
  Pay: $90,000.00-$110,000.00 per year

Benefits:

• Dental care
• Extended health care
• Life insurance

Work Location: In perso

Please refer the Job description for details