Process Engineer

Job description

Process Engineer

Your role:
At Millipore Sigma the Process Engineer will work in a dynamic environment supporting the manufacture and testing of high purity filters with a focus on quality, process control/improvements, electro-mechanical assembly and material handling.  The successful candidate will be an enthusiastic team player with high energy and strong engineering skills. 

 

·  Design and upgrade electromechanical equipment to improve reliability and yield.
·  Maintain efficiency and upkeep / upgrade of critical manufacturing equipment.
·  Identify and improve yield loss and scrap opportunities.
·  Develop and recommend new processes and technologies which demonstrate levels of statistical control to achieve cost effectiveness and improved product quality.
·  Establish operating equipment specifications and improve manufacturing techniques.
·  Inspect performance of machinery, equipment and tools to verify their efficiency and investigate and initiate corrective action of problems and deficiencies to ensure product quality.
·  Develop and/or implement systems improvement projects and supports maintenance and production groups in resolving technical and engineering issues.
·  Provide process on assigned Corrective Action Preventive Action (CAPA).
·  Review capital equipment fabrication activities to ensure manufacturing, construction, installation, and operational testing conform to functional specifications, regulatory safety standards, and user requirements.
·  Develop cost estimates, obtains quotes, and generates capital requests to support new processes and capital equipment purchase.
·  Lead and participate in Equipment and Process Validations activities per Current Good Manufacturing Practices (cGMP) regulations for Medical Device manufacturing.
·  Ensure that product quality features meet product specifications and comply with process validation requirements.
·  Generate, review and approve engineering, manufacturing and quality procedures necessary to support equipment validation/revalidation, launch, and normal production schedules.
·  Facilitate training for individuals involved with the operation and maintenance of processes and equipment introduced to the manufacturing department.
·  Initiate, review/approve change requests, and develops implementation solutions to support operational needs.

 
Who you are:
Basic Qualifications:

·  Bachelors Degree in Electrical Engineering, Mechanical Engineering, Chemical Engineering, or related discipline 

Preferred Qualifications:

·  1+ year of experience in an FDA regulated medical device manufacturing facility, pharmaceutical facility or similar regulated industry supporting automated or manual assembly processes.
·  Master’s degree in Electrical, Mechanical or Chemical Engineering or related discipline. 
·  Instrumentation and PLC / code knowledge / experience
·  Automation and electromechanical knowledge / experience
·  Lean 6 Sigma knowledge / experience

 

Job Requisition ID: 210665

Location: Jaffrey

Career Level: B - Recent University Graduate(

Nearest Major Market: Bellows Falls
Nearest Secondary Market: Keene
Job Segment: Medical, CAPA, Pharmaceutical, Lean Six Sigma, Medical Device, Healthcare, Management, Science