Sterility Assurance Validation Specialist I

Simtra-Biopharma-Solutions is hiring a Sterility Assurance Validation Associate I in Bloomington, Indiana. The role includes managing project qualifications, validating equipment, and ensuring compliance with regulatory standards. Candidates must have a BS in a science-related field or equivalent experience in the pharmaceutical industry. Key responsibilities involve documenting SOPs, conducting equipment studies, and collaborating with clients. This position is full-time, onsite, with an emphasis on quality assurance and continuous improvement. #J-18808-Ljbffr