Job Details

ID #49560565
State Minnesota
City Littlecanada
Job type Contract
Salary USD TBD TBD
Source Experis
Showed 2023-03-27
Date 2023-03-26
Deadline 2023-05-25
Category Et cetera
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R&D Engineer Sr.

Minnesota, Littlecanada, 55133 Littlecanada USA

Vacancy expired!

Experis, a ManpowerGroup company has an exciting contract opportunity for one of our key clients, a Fortune 500 American global biopharmaceutical company that is engaged in the discovery, development, and manufacture of healthcare products.

Job Description:

Below are some key highlights of the position:

Project Details:

Job Title:

Sr. R&D Engineer

Client Location:

St. Paul Minnesota

Role:

Onsite

Contract/Direct Hire

09 Months

Shift 1st- 09:00 AM to 05:00 PM

Education:

Bachelor's degree plus 12+ years of related work experience with a complete understanding of specified functional area, or an equivalent combination of education and work experience. Advanced degree preferred.

Key Responsibilities and Duties:

  • Responsible for providing technical support in the creation and the development of new medical device products (invasive and non-invasive).
  • Responsible for compliance with applicable Corporate and Divisional Policies and procedures
  • Identifies and initiates programs which result in innovative application of existing or new products or technologies.
  • Conduct experiments and/or develop strategies for consideration that extend beyond known scientific and engineering precedents.
  • Provides periodic communication updates to management on future business direction and problem resolution.
  • Researches, develops, designs, and evaluates mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment.
  • Write operational concept documents to describe changes and integrate information into system architecture specification
  • Work with cross-functional teams to understand and meet regulatory standard updates (e.g., EUMDR, 60601) Document issues, own and solve issues delegated to Systems Engineering.
  • Ability to work independently with minimal supervision. Maintain high standards for content completion, integrity, and regulatory & standards compliance. Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments.

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Vacancy expired!

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