05 Oct, 2021

Process Engineer

  • Merck
  • Jaffrey, NH, USA
Process Engineer Chemicals

Job Description

Your role:
At MilliporeSigma, 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. 

 

  • Maintains efficiency and upkeep of critical manufacturing equipment through effective troubleshooting techniques.
  • Identifies and improves yield loss and scrap opportunities.
  • Develops and recommends new testing processes and technologies to achieve cost effectiveness and improved product quality.
  • Establishes operating equipment specifications and improves manufacturing techniques.
  • Inspects performance of machinery, equipment and tools to verify their efficiency and investigates and initiates corrective action of problems and deficiencies to ensure product quality.
  • Develops manufacturing processes that demonstrate levels of statistical control.
  • Validates new equipment and process changes.
  • Develops and/or implements systems improvement projects and supports maintenance and production groups in resolving technical and engineering issues.
  • Provides process on assigned Corrective Action Preventive Action (CAPA).
  • Trains departmental technicians and operators to ensure sufficient expertise exists within the manufacturing work centers.
  • Reviews capital equipment fabrication activities to ensure manufacturing, construction, installation, and operational testing conform to functional specifications, regulatory safety standards, and user requirements.
  • Investigates and develops new processes required to improve manufacturing operations and processes.
  • Develops cost estimates, obtains quotes, and generates capital requests to support new processes and capital equipment purchase.
  • Leads and participates in Equipment and Process Validations activities per Current Good Manufacturing Practices (cGMP) regulations for Medical Device manufacturing.
  • Ensures that product quality features meet product specifications and comply with process validation requirements.
  • Generates, reviews and approves engineering, manufacturing and quality procedures necessary to support equipment validation/revalidation, launch, and normal production schedules.
  • Facilitates training for individuals involved with the operation and maintenance of processes and equipment introduced to the manufacturing department.
  • Generates engineering procedures and reviews and approves manufacturing standard operating procedures.
  • Develops validation protocols and reports in support of cGMP requirements.
  • Initiate, reviews/approves change requests, and develops implementation solutions to support operational needs.

 

 

Who you are:

Basic Qualifications:

  • Bachelors of Science Degree in Electrical, Mechanical or Chemical Engineering (or closely related field)

 

Preferred Qualifications:

  • Experience in an FDA regulated medical device manufacturing facility, pharmaceutical facility or other regulated industry supporting automated or manual assembly processes
  • Instrumentation and PLC / code knowledge a plus
  • Lean 6 Sigma experience with green or black belt preferred

Apply Now