The ideal candidate will have 5+ years of experience in validation of sterile fill finish processes and equipment including extensive cleaning validation experience Responsibilities Design/Author/Review/Approve/Execute qualification/validation documentation and cycle development studies in line with the standard approval process. […]
Serve as validation representative for cross functional projects and represent the validation team at global technical forums Drive compliance of Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP)...