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ProPharma Group seeks a Program Lead/Sterility Assurance Review Senior Consultant to oversee a retrospective product review workstream in Kansas City, KS on site for a 2-3 month engagement. The role leads the review methodology, coordinates lot assessments, and delivers final reports to ensure regulatory alignment. You will act as the primary client contact, provide technical oversight of sterility review activities, and guide the team to maintain scientific rigor and FDA remediation alignment.

Also on the board Same function, level within a rung

Level

Lead

Location

Kansas City, KS

Occupation

Quality Control Systems Managers

Industry

Other Management Consulting Services

Posted

yesterday

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