Job Description

• Previous experience going live with electronic MBR system from paper. Design spec review is very important. 
• Review of initial MES (Manufacturing Execution System) design specifications against the master record or process transmittal.
• Review of master batch record in MES to ensure the build of the record in the electronic system matches the design specification.
• Active participation at pre-production execution meetings with manufacturing and MES designers to test the build for accuracy, process flow, etc.
• Previous experience with Werum PAS-X highly preferred.

Qualifications

• Prior experience with Werum PAS-X
• Understanding of biologics manufacturing operations is preferred 
• Good organizational skills and attention to detail 
• Requires good written, verbal and interpersonal communication skills and the ability to effectively interact cross functionally. 
• Ability to handle multiple assignments and changing priorities. 
• Ability to learn and utilize computerized systems for daily performance of tasks 
• Ability to prioritize, manage multiple tasks, and meet deadlines

Additional Information

All candidates must be legally eligible to work in the United States. We are an equal opportunity employer. M/F/D/V

ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.