1+ years of industrial experience in a cGMP manufacturing setting.
Demonstrated experience in process development or manufacturing support of vaccines or biopharmaceuticals.
Working knowledge and work experience in manufacturing operations.
Demonstrated ability in technology transfer, scale-up, and project support
Must be able to work with and lead multifunctional teams.
Strong collaboration skills and proven success in a team based environment
- Excellent written, oral communication, and computer skills.
Provide significant shopfloor technical support during clinical and commercial operations
Support investigation teams for process related deviations, apply root cause and data analysis tools to develop science based, data driven results
Manufacturing support activities including process mapping, process troubleshooting, process improvement, process management and supporting DOE experiments based on Six-Sigma methodologies
Participate in technology transfer activities, drive resolution to technical challenges, and collaborate with teams for resolution of issues
Participate in the preparation for process scale-up, process transfer and process validation.
Execute technical studies and process validation assessments, protocols, and reports.
Assist in the design and execution of technical studies in qualification of new equipment, process validation, and scale-down studies to support scale-up, cycle development, and process changes.
You may apply for this position online by selecting the Apply now button.
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