MVProject Manager

Position: MV01-072825 Project Manager (IN)
Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas:
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

* Project Manager

Job Summary:

We are looking for a Project Manager with hands-on experience in Validation to provide full oversight of equipment qualification activities. This role will focus on Autoclaves, Fillers, and Part washers within a regulated manufacturing environment. The ideal candidate will be responsible for coordinating all validation tasks, identifying next steps, and ensuring alignment across teams and vendors. Safety knowledge is a plus.

Key Responsibilities:

* Provide full oversight and coordination of validation projects for Autoclaves, Fillers, and Part washers.

* Act as the central point of contact for all activities related to equipment qualification.

* Coordinate cross-functional teams to ensure timely execution of project milestones.

* Continuously assess project status and determine what is needed for upcoming activities.

* Lead planning and scheduling of validation tasks including URS, FAT/SAT, IQ, OQ, and PQ.

* Ensure compliance with cGMP, FDA, and internal quality and documentation standards.

* Track timelines, manage risks, escalate issues, and communicate progress to stakeholders.

* Foster a strong culture of safety and ensure safety practices are integrated into all project activities.

Qualifications:

* Bachelors degree in Engineering, Life Sciences, or a related field.

* 5+ years of experience in validation and project coordination within pharmaceutical or regulated environments.

* Proven experience qualifying Autoclaves, Fillers, and Part washers.

* Strong understanding of validation documentation and regulatory compliance (GMP, FDA).

* Excellent coordination, planning, and leadership skills.

* Safety certification or demonstrated safety awareness is a plus.

Schedule:

Full-time, on-site in Indianapolis, IN