Manufacturing Engineer

job
  • Sunrise Systems, Inc.
Job Summary
Location
Portsmouth ,NH 00215
Job Type
Contract
Visa
Any Valid Visa
Salary
PayRate
Qualification
BCA
Experience
2Years - 10Years
Posted
23 Jan 2025
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Job Description

Job Title: MES Engineer

Location: 101 International Drive, Portsmouth, NH 03801

Duration: 6+ months contract to begin with

Position Type: Hourly Basis on W2 only


Job Summary:

The MES Engineer Level 2 is responsible for supporting activities such as requirements gathering, testing, implementation and use of Manufacturing Execution Systems (MES). Position is expected to operate with some supervision and some autonomy.


Job Description(Key Accountabilities)

Safety

• Performs all work safely and meets the requisite training requirements


Manufacturing Support

• Develop technical knowledge on manufacturing equipment and process automation systems

• Manage resolution of equipment breakdowns and quality issues in the suites

• Provide SME support to Manufacturing and other departments for the design and operation of process equipment.

• Conduct troubleshooting and technical analyses on manufacturing equipment and process control systems including PI data analyses, CIP/SIP circuit review, flow path analyses, code review/troubleshooting, etc.

• Assist with tech transfer of new processes into the facility

• Complete change request lot assessments to support lot release

• Participates in IPT/JPT meetings as MES representative Projects

• Planning and execution of plant projects involving automation changes and process improvements including lump sum capital projects

• Execute test scripts (design, execution, simulation, wet testing)

• Own change requests and complete change request tasks to support project completion

• Perform change request assessments Deviations / RCAs

• Assist the Quality department with deviation investigations

• Participate in RCAs as MES representative

• Assist with completion of CAPA actions

• Participates in quality risk assessments Documentation

• Review/revise automation and Manufacturing related SOP's, Functional Specifications, and work instructions as a result of CAPA, equipment/process changes, error prevention activities, etc.

• Complete MES review/approval of batch records

• Author and review test protocols


Work Experience:

Automation - 0-4 experience

Pharma/Biotech - 0-4 experience


Skills

• Ability to effectively communicate at all levels

• Ability to secure relevant information and identify key issues and relationships from a base of information.

• Ability to evaluate engineering problems and be able to devise cause and effect relationships and propose solutions.

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