Manufacturing Engineer(Medical devices) - Minnetonka, United States - Intellectt Inc

Description

ole: Manufacturing Engineer

Location: Westbrook, ME

Duration: 6-12 Months

The Opportunity

s.

As a Process Development Engineer, you will perform analyses to develop process technologies

based on product design and performance requirements. Provides technical information concerning

manufacturing or processing techniques, materials, properties and process (advantages/limitations)

engineering planning. Selects techniques to solve problems and make sound design

recommendations.

What You'll Work On

 Execution of Process Validations including Test Method Validation (TMV), Inspection Method

Validation (IMV), Installation Qualification (IQ), Operational Qualification (OQ), Performance

Qualification (PQ), Product Performance Qualification (PPQ)

 Write and release IQ reports

 Troubleshoot process equipment

 Assist in developing processes based on product specifications and in consideration to

process and test method capabilities.

 Understand work environment issues (i.e. OSHA regulations, etc.).

Required Qualifications

 B.S. in engineering

 3+ years experience in process development or manufacturing process engineering

 Experience developing and validating medical device manufacturing equipment, fixtures, and

technologies with an emphasis on design for manufacturability (DFM) preferred.

 Experience performing installation qualifications (IQ).

Preferred Qualifications

 Background in introducer/catheter processing

Thanks & Regards

Pavani Chiluka

Recruitment Lead

Direct:

Office: ; Ext: 221

Intellectt Inc

#517 Route 1 South, Suite 1115 Iselin, NJ 08830.

--Email is the best way to reach me