CQV Project Manager — Pharma Manufacturing & Validation

A leading engineering firm in Indiana is seeking a skilled Project Manager to oversee projects in a regulated manufacturing environment. The candidate will manage the entire project lifecycle, ensuring compliance with cGMP and FDA regulations. This role demands at least 10 years of project management experience within the pharmaceutical sector and strong leadership skills. The ideal candidate will develop project master plans, coordinate with teams, and ensure all deliverables meet client expectations while adhering to regulatory requirements.
#J-18808-Ljbffr