Overview
On Site
Full Time
Skills
Statistical Process Control
Performance Monitoring
Conflict Resolution
Problem Solving
ROOT
Cross-functional Team
Continuous Improvement
Cost Reduction
Project Management
Project Coordination
Reporting
Management
Documentation
Technical Support
Auditing
Accountability
Regulatory Compliance
Chemistry
Mechanical Engineering
Process Manufacturing
Project Engineering
Pharmaceutics
Forms
Communication
English
Manufacturing
Supply Chain Management
Operational Excellence
EHS
Job Details
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 analyse 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 following 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 Client's EHS program.
- BS or MS in Chemistry or Engineering (Chemical, Mechanical, Bio-chemical)
- 5-7 years of technical experience in Process/Manufacturing/Project Engineering or similar role.
- Technical knowledge in fundamentals of pharmaceutical liquid-solid dosage forms processing.
- Effective verbal and written communication skills in English.
- Manufacturing, Quality, Supply Chain, Operational Excellence, Engineering, EHS.
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