Medical Device - Bio-Medical Engineer - mid & Sr.

  • Contract

Company Description

MEDVACON is conducting a search for our leading Medical Device client in Columbia, MD

Hiring for mid and Sr. level Bio-Medical Engineers on-sie in Columbia, MD

Job Description

Mid to Sr. level Biomedical Engineers for a 2-year assignment on-site in Columbia MD.  Candidates must be local to Columbia, MD or willing to temporarily relocate at their own expense.

SUMMARY:

Works as a team member on cross-functional teams throughout the development process

Performs or oversees biomedical/mechanical engineering, design, and development work

Develops design concepts and ideas for new products and product improvements

Develops prototypes of design concepts for engineering testing and evaluation

Reviews/approves SOPs, test protocols, laboratory research reports and provides laboratory oversight as needed

Performs human factors (usability studies), market assessment, or pre-clinical research

Responsible for adhering to design controls and documenting all product development work in a Design History File

Lead risk analysis activities

Comply with FDA Regulation and Guidance For Combination Products

 

 

 

Qualifications

REQUIREMENTS:

Minimum Bachelors in Science, Biomedical Engineering, Mechanical Engineer

  • 3-5 years medical device development experience for mid-level
  • 5-7 years exp for the Sr. level


Conceptual design skills and experience with a variety of manufacturing methods (e.g. injection molding, machining, etc.

Human Factors and usability engineering

Software:  Minitab, SolidWorks, (Basics), Microsoft Office

Regulatory Knowledge and Experience: 
CFR 820
ISO 14971, 13485
CFR 210/211

 

 

Additional Information

Please attach a WORD resume to your on-line application.

This is a 2 year contract assignment on-site in Columbia, MD.   NOT a perm job.

No expenses or benefits are available for this assignment.

No!  Agencies please do not submit your candidates.  NO C/C with other employers.

W2 or 1099 directly with a consultant only.

All your information will be kept confidential according to EEO guidelines.