Engineering Specialist III

ID# DCFL27097

dinaliC is an international consulting firm specialized in projects for numerous industries. We are dedicated to provide contract and permanent opportunities for skilled professionals in their area or areas of expertise

JOB OVERVIEW 

Proficient in design control requirements, the individual in this position develops standard operating procedures, specifications, and provides technical transfer and process validation support. Minimizes sample and scrap waste, assesses reliability and risks based on validated data, identifies root causes of problems, and reduces or eliminates sources of variation. Leads risk analysis assessments in compliance with appropriate regulatory standards. Audits and approves manufacturing, quality, engineering and validation documents for conformance to business practices, departmental procedures and regulatory standards. Provides data and documentation in support of the development of validation strategies, protocols and reports. Acts as liaison to the regulatory affairs department to perform initial regulatory review of all engineering changes and modifications to products. Provides sampling plans and prepares/approves testing and inspection methods for evaluation and testing of components and products in support of design verification, design validation, shelf life testing, etc. Ensures/leads the validation of testing methodologies. Provides support and expertise in reliability planning and reliability growth demonstration during new product development. 

Generally requires (6-8) years related experience 

University/Bachelors Degree or Equivalent

Position Details:

Medical Device

Engineering

Start Date: 
9-9-2013
End Date: 
12-31-2013

MIRAMAR, FL

CON_W2

37.5

DCFL27097

No

No