Overview
Remote
Depends on Experience
Accepts corp to corp applications
Contract - W2
Contract - Independent
Contract - 6 Month(s)
Skills
Manufacturing Execution Systems
MES
CIP
SIP
Root Cause Analysis
RCA
Corrective and Preventive Actions
CAPA
Preventive
Corrective
design
execution
simulation
Equipment
Process
Manufacturing
wet
Whole Effluent Toxicity
Pharma
Pharmaceutical
BioTech
Job Details
Project Engineer / Manufacturing Execution Systems Engineer / MES Engineer
REMOTE
Duration: - 6 Months+
MES Engineer 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.
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
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