CQV Program Manager - GMP Manufacturing Leader

A pharmaceutical company in Indiana is seeking a Mid-Senior level Project Manager to oversee capital projects in Oral Solid Dosage manufacturing. The ideal candidate will have 7–10 years of experience in pharmaceutical manufacturing and possess strong skills in project management, budgeting, and cross-functional collaboration. This full-time role is essential for ensuring project alignment with corporate goals and requires onsite work at a GMP facility. #J-18808-Ljbffr