Project Manager

  • location: Deerfield, IL
  • type: Contract
  • salary: $52 - $68 per hour
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job description

Project Manager

Contract position: Medical Device Manufacturing client has an immediate need in Deerfield IL for a Project Manager. We are looking for candidate that have experience in EU MDR or Engineering (Medical Device) or Medical Affairs or Post Market Surveillance. This is a contract position expected to last 1 year, could be longer based on performance, possible temp to hire. Will consider non-local candidates that are willing to relocate at their own expense! Apply Now!

Responsibilities for the Project Manager
  • Accountable for core team performance, project schedule and execution, budget commitments and spend
  • Interacts through project updates and reviews with all functions and levels of management ensuring effective ongoing communications across teams and stakeholders
  • Ensures identification and communication of project risks, development of risk plan and proactive management of risk response strategies
  • Anticipates potential conflict situations for proactive solutions and manages conflict situations to result in win-win outcomes
  • Supports the Medical Affairs & Post Market Surveillance Workstream Leadership in managing the successful delivery of the Medical Affairs & Post Market Surveillance deliverables in accordance with timelines and their respective dependencies
  • Understand the Medical Affairs & Post Market Surveillance required deliverables and the cross functional nature of resources required to develop/review/approve these deliverables; ensure project process aligns with relevant Baxter enterprise processes
Requirements for the Project Manager

  • A minimum of an MBA/MS or Bachelor's with equivalent plus 7 years project management experience and 10 years of product life cycle experience
  • 5+ yrs of Project Management Experience
  • Medical device / Post Market Surveillance experience
  • Experience/Background in EU MDR or Engineering (Medical Device) or Medical Affairs or Post Market Surveillance
  • Experience with complex multifunctional regulatory driven projects implementing new processes/capabilities
  • Previous Medical Device / Pharmaceutical / Biotechnology industry experience be required
  • Software: MS Project, Excel (Pivot Table & V-Lookups, reporting, strongly preferred), Word, Outlook, PowerPoint, & SharePoint

  • Paid Vacation
  • 401K
  • Health Insurance, and more...
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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