Engineer Process Support II
Spectraforce Technologies, North Chicago, IL, United States
Title: Engineer Process Support II
Duration: 12 Months
Location: North Chicago, IL 60064 (hybrid schedule - 3 days onsite/2 days remote)
Working Days: Monday - Friday and 8am - 5pm
Top 3-5 Skills
Strong Technical Background
Packaging Engineering/Material Science degree preferred
Initiative/Self Motivated
Good communication Skills (oral and Written)
Description
Engineering background with experience in:
Packaging design
Protocol/report writing
Understanding of packaging commodity specifications (Such As Labels, Carton, Leaflets, bottles, Corrugate boxes, etc)
Define testing parameters and instructions to be executed by Lab Techs.
Data review and ability to provide conclusions
Managing projects independently
Participate in internal/external meetings and lead meetings occasionally
Work with the Commodities Supplier, if required by the project/task assigned.
Healthcare/Pharma experience preferred
Responsibilities
Lead projects in manufacturing process areas to achieve process efficiencies such as increase in process yield, quality improvements, cycle time/throughput, and cost reduction initiatives.
Gather and analyze process data using statistical process control methodology. Develop action plan to increase process robustness, prevent product loss, and control quality impact. Participate in process performance monitoring such as Track & Trend.
Responsible for providing technical support in the resolution of shop floor situations and executing assigned tasks as required by the operational area.
Lead investigations by following a structure problem solving approach and employing sound, scientific principles when identifying root cause and developing recommendations related to product and process. Generate technical justification to support and/or document process deviations/investigations and determine impact in product quality, yield, and product registration.
Part of cross-functional team responsible for implementation of site projects/initiatives (continuous improvement, cost reduction, capacity increase, etc.) that lead to process remediation.
Project management of smaller team, short duration projects within larger projects. Responsibility may include project coordination, monitoring, reporting, meeting management, and team communication.
Lead the implementation of process validation for operational changes, new raw materials, and introduction of new process/technology. Generate technical justification determining impact of change and protocols/reports/manufacturing documents that support its execution. Assist the execution of experimental, demonstration, and validation lots.
Maintain up-to-date product process documentation and assure they are in compliance with applicable procedures and regulations. Writes justification memos and scientific reports of quality controls and manufacturing documents.
Provide scientific and technical support during regulatory audits and agency inspections.
Demonstrate accountability and responsibility for EHS performance and compliance through active participation and support of EHS program.
Qualifications
BS or MS in Chemistry or Engineering (Chemical, Mechanical, Bio-chemical)
3-5 years' of technical experience in Process/Manufacturing/Project Engineering or similar role. Candidates with 2 years of experience on a similar role can be considered.
Technical knowledge in fundamentals of pharmaceutical solid dosage forms processing.
Effective verbal and written communication skills.
Key Stakeholders
Manufacturing
Quality
Supply Chain
Operational Excellence
Engineering
EHS
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Duration: 12 Months
Location: North Chicago, IL 60064 (hybrid schedule - 3 days onsite/2 days remote)
Working Days: Monday - Friday and 8am - 5pm
Top 3-5 Skills
Strong Technical Background
Packaging Engineering/Material Science degree preferred
Initiative/Self Motivated
Good communication Skills (oral and Written)
Description
Engineering background with experience in:
Packaging design
Protocol/report writing
Understanding of packaging commodity specifications (Such As Labels, Carton, Leaflets, bottles, Corrugate boxes, etc)
Define testing parameters and instructions to be executed by Lab Techs.
Data review and ability to provide conclusions
Managing projects independently
Participate in internal/external meetings and lead meetings occasionally
Work with the Commodities Supplier, if required by the project/task assigned.
Healthcare/Pharma experience preferred
Responsibilities
Lead projects in manufacturing process areas to achieve process efficiencies such as increase in process yield, quality improvements, cycle time/throughput, and cost reduction initiatives.
Gather and analyze process data using statistical process control methodology. Develop action plan to increase process robustness, prevent product loss, and control quality impact. Participate in process performance monitoring such as Track & Trend.
Responsible for providing technical support in the resolution of shop floor situations and executing assigned tasks as required by the operational area.
Lead investigations by following a structure problem solving approach and employing sound, scientific principles when identifying root cause and developing recommendations related to product and process. Generate technical justification to support and/or document process deviations/investigations and determine impact in product quality, yield, and product registration.
Part of cross-functional team responsible for implementation of site projects/initiatives (continuous improvement, cost reduction, capacity increase, etc.) that lead to process remediation.
Project management of smaller team, short duration projects within larger projects. Responsibility may include project coordination, monitoring, reporting, meeting management, and team communication.
Lead the implementation of process validation for operational changes, new raw materials, and introduction of new process/technology. Generate technical justification determining impact of change and protocols/reports/manufacturing documents that support its execution. Assist the execution of experimental, demonstration, and validation lots.
Maintain up-to-date product process documentation and assure they are in compliance with applicable procedures and regulations. Writes justification memos and scientific reports of quality controls and manufacturing documents.
Provide scientific and technical support during regulatory audits and agency inspections.
Demonstrate accountability and responsibility for EHS performance and compliance through active participation and support of EHS program.
Qualifications
BS or MS in Chemistry or Engineering (Chemical, Mechanical, Bio-chemical)
3-5 years' of technical experience in Process/Manufacturing/Project Engineering or similar role. Candidates with 2 years of experience on a similar role can be considered.
Technical knowledge in fundamentals of pharmaceutical solid dosage forms processing.
Effective verbal and written communication skills.
Key Stakeholders
Manufacturing
Quality
Supply Chain
Operational Excellence
Engineering
EHS
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