Process Engineer - Industrial Automation ID:9112453473
Now hiring in Lawrence, KS Our client - a growing company with multiple plants in the US, needs a Process Engineer at their KS plant expanding to manufacture pharmaceutical productsExcellent salary up to $90K
sponsorship for H1B Transfer or OPT Visa
Relocation assistance
Full Benefit PackageRelocation:
YES - Client offers relocation assistance and payments for expenses
Benefits:
Full package for medical, dental insurance, 401K, etcGroup Info:
Be part of the medical device and pharmaceutical contract manufacturing site with around 100
employees and expected to grow to 150 people soon due to major expansion in Pharma manufacturingThe new operation expansion is for Pharma - Blow Fill Cap - BFC of Sterile SolutionsThe Engineering group has around 6 people including Project, Automation, ManufacturingThis role will report to the Director of EngineeringNote 1:
The client will sponsor for H1B Transfer and OPT Visa if needed Coordinates and assists with all process and equipment changes and implementation of new systems, equipment, and product transfersFacilitates Process Development meetings, keeping track of all projects and their statusResearches new processes and suggests improvement for continued excellence and helps on troubleshooting existing processes and equipmentDesigns, redesigns, and implements systems and equipment procedures used in manufacturing facilitiesMain duties include testing and monitoring equipment, updating current system processes, and conducting risk assessmentsParticipates in continuous improvement and Kaizen projects in support of the Quality SystemEngineering& Validation:
Represents engineering and validation for new systems and equipment by providing technical information, writing, and review of URS documentsSupports engineering and validation efforts by performing FAT and SAT commissioning activitiesWrites and revises procedures to support new systems or new product realization projectsMaintains professional and technical knowledge by attending educational workshops and reviewing professional publicationsApply general engineering principles to develop and implement capital projects that will reduce costs, improve operating efficiency, progress quality, and improve safetyDeveloping, configuring and optimizing end-to-end industrial processes, from ideation to certification Conduct research to develop new and improved processes for manufacturingEstablish safety procedures for individuals working with dangerous chemicalsDesign and plan equipment and room layoutConduct tests and monitoring the process performance throughout productionTroubleshoot problems associated with manufacturing processesEvaluate processes and equipment to ensure compliance with environmental and safety regulationsEstimate production costsRun risk assessments of the equipment and processes being usedProvide engineering support for new equipment upgrades and special projectsDevelop project plans and schedules; track project progressionReport on project progress, limiting factors and issues, changes in project scope, develop contingency plans, and resolve issues impeding progressCollaborate with production personnel to develop new projects, identify limiting factors in current projects, and create/maintain relationshipsAssist Product Development with engineering support for new product linesPurchasing:
Uses the purchasing system to procure production and maintenance suppliesActively uses the DCR System to change or add new document requirementsCIMP System:
Assists Managers and leads projects for continuous improvement and Kaizen eventsSupports the nonconformance system through reporting of Nonconformances and supporting Quality in investigation activitiesTraining:
Provides training to other employees to support continued competencyFacility Maintenance:
Actively review reports and documents for compliance to requirements and troubleshoots issuesProvides hands-on training on various systemsBS Degree in Engineering or related field 1 year of hands-on experience with equipment, processes, and systemsExperience Developing Standards, Process Improvement, Decision Making, Troubleshooting, Project coordination and management, P&ID reading, CAD or similar engineering software, commissioning and qualification principles, ISO SystemsMaster's Degree in Engineering Familiar with ISPE Good Engineering Practices guidelinesExperience in ISO standard& Quality SystemsCertification and experience in program management, lean manufacturing, commissioning, and qualificationExperience in Injection Molding, Blow Molding& Sterile Aseptic Filling Operations Contract Manufacturing experience working closely with customers and clients BioPharma, Pharma, Manufacturing, Process, Project, Engineer, FDA, Validation, commissioning, Sterile Aseptic filling, BFC,H1B, OPT Recommended Skills Automation Business Process Improvement Cad Continuous Quality Improvement (Cqi) Contract Manufacturer Decision Making Apply to this job.
Think you're the perfect candidate? Apply on company site Estimated Salary: $20 to $28 per hour based on qualifications.
sponsorship for H1B Transfer or OPT Visa
Relocation assistance
Full Benefit PackageRelocation:
YES - Client offers relocation assistance and payments for expenses
Benefits:
Full package for medical, dental insurance, 401K, etcGroup Info:
Be part of the medical device and pharmaceutical contract manufacturing site with around 100
employees and expected to grow to 150 people soon due to major expansion in Pharma manufacturingThe new operation expansion is for Pharma - Blow Fill Cap - BFC of Sterile SolutionsThe Engineering group has around 6 people including Project, Automation, ManufacturingThis role will report to the Director of EngineeringNote 1:
The client will sponsor for H1B Transfer and OPT Visa if needed Coordinates and assists with all process and equipment changes and implementation of new systems, equipment, and product transfersFacilitates Process Development meetings, keeping track of all projects and their statusResearches new processes and suggests improvement for continued excellence and helps on troubleshooting existing processes and equipmentDesigns, redesigns, and implements systems and equipment procedures used in manufacturing facilitiesMain duties include testing and monitoring equipment, updating current system processes, and conducting risk assessmentsParticipates in continuous improvement and Kaizen projects in support of the Quality SystemEngineering& Validation:
Represents engineering and validation for new systems and equipment by providing technical information, writing, and review of URS documentsSupports engineering and validation efforts by performing FAT and SAT commissioning activitiesWrites and revises procedures to support new systems or new product realization projectsMaintains professional and technical knowledge by attending educational workshops and reviewing professional publicationsApply general engineering principles to develop and implement capital projects that will reduce costs, improve operating efficiency, progress quality, and improve safetyDeveloping, configuring and optimizing end-to-end industrial processes, from ideation to certification Conduct research to develop new and improved processes for manufacturingEstablish safety procedures for individuals working with dangerous chemicalsDesign and plan equipment and room layoutConduct tests and monitoring the process performance throughout productionTroubleshoot problems associated with manufacturing processesEvaluate processes and equipment to ensure compliance with environmental and safety regulationsEstimate production costsRun risk assessments of the equipment and processes being usedProvide engineering support for new equipment upgrades and special projectsDevelop project plans and schedules; track project progressionReport on project progress, limiting factors and issues, changes in project scope, develop contingency plans, and resolve issues impeding progressCollaborate with production personnel to develop new projects, identify limiting factors in current projects, and create/maintain relationshipsAssist Product Development with engineering support for new product linesPurchasing:
Uses the purchasing system to procure production and maintenance suppliesActively uses the DCR System to change or add new document requirementsCIMP System:
Assists Managers and leads projects for continuous improvement and Kaizen eventsSupports the nonconformance system through reporting of Nonconformances and supporting Quality in investigation activitiesTraining:
Provides training to other employees to support continued competencyFacility Maintenance:
Actively review reports and documents for compliance to requirements and troubleshoots issuesProvides hands-on training on various systemsBS Degree in Engineering or related field 1 year of hands-on experience with equipment, processes, and systemsExperience Developing Standards, Process Improvement, Decision Making, Troubleshooting, Project coordination and management, P&ID reading, CAD or similar engineering software, commissioning and qualification principles, ISO SystemsMaster's Degree in Engineering Familiar with ISPE Good Engineering Practices guidelinesExperience in ISO standard& Quality SystemsCertification and experience in program management, lean manufacturing, commissioning, and qualificationExperience in Injection Molding, Blow Molding& Sterile Aseptic Filling Operations Contract Manufacturing experience working closely with customers and clients BioPharma, Pharma, Manufacturing, Process, Project, Engineer, FDA, Validation, commissioning, Sterile Aseptic filling, BFC,H1B, OPT Recommended Skills Automation Business Process Improvement Cad Continuous Quality Improvement (Cqi) Contract Manufacturer Decision Making Apply to this job.
Think you're the perfect candidate? Apply on company site Estimated Salary: $20 to $28 per hour based on qualifications.
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