Company:
Synectics
Location: North Chicago
Closing Date: 07/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Description:
- 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 and 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.
- BS or MS or PhD in Chemistry or Engineering (Chemical, Mechanical, Bio-chemical, or other relevant scientific field)
- 5-7 years' of technical experience in Process/Manufacturing/Project Engineering or similar role.
- Technical knowledge in fundamentals of pharmaceutical process (sterile product manufacturing).
- Effective verbal and written communication skills in both English.
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