• US Citizen

• Green Card

• EAD (OPT/CPT/GC/H4)

• H1B Work Permit

• Corp-Corp

• W2-Permanent

• W2-Contract

• Contract to Hire

• Consulting/Contract

• UG :- - Not Required

• PG :- - Not Required

• No of position :- ( 1 )

• Post :- 26th Dec 2023

• Spotlight Call notes:
  Onsite from 8-5pm.  Lake Forest, IL 60045
• Main task of the project is Remediation of technical documentation to comply with new EU regulation IVDR.   
• The new In Vitro Diagnostic Regulation (IVDR) aims to harmonize regulatory framework across the European Union (EU) to ensure the safety and performance of devices.
• Manage the process and work with and lead cross functional teams and stakeholders.
• Best candidates will have Regulatory experience with medical products.
• At least 5 years’ experience preferred. PMP nice to have.
• Excellent communication skills 
• Reporting to sr. management
• Risk elevation evaluations
• Conduct meetings

Manages/directs the activities and people associated with small to large scale projects with a focus on any or several non-IT business applications and disciplines. Manage/direct all facets of single or multiple, multidimensional, mission-critical projects through the Full Project Life Cycle. Collaborate/work with project sponsors, business units and users to identify project scope and focus, develop or monitor project initiatives, implement project requirements/plans/processes/tools, assign/guide/monitor project staff, and assure project success. Deliver quality project solutions to business problems or issues within defined budgets and/or timelines. Provide expert project guidance/support proactively through project completion. Provide tracking, reporting, and presentation to management and users.