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Process Engineer III - Pharmaceutical Industry - NJ - Hybrid
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- 3) Acts as technical and coordination focal point for site and external CMO"s for multi-site projects regarding technical documentation of package requirements.
- Subject Matter Expert (SME) for development and validation, health authority inspections, and investigations.
- Responsible for process design and continuous improvements, support execution and documentation of development and/or validation studies and lead or supervise groups and/task force in the planning of engineering, investigational, definition and process validation runs.
- Execute life-cycle design and industrialization of upstream processes, products and associated test methods for Phase 3 and licensed products (new vaccines and biopharmaceuticals AND life-cycle improvements) to assure commercialization of robust, compliant, and efficient processes and test methods for vaccines and biopharmaceuticals.
- Input to design space/DOE studies through establishment of scale-up/scale-down parameters utilizing engineering fundamentals (mixing, mass/heat transfer, modeling, dimensionless parameters, etc.)
Expired 11 days agoInactive Job
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