MVProject Manager
Listed on 2025-12-11
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Engineering
Quality Engineering, Pharma Engineer
Location: Indianapolis
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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, elevate issues, and communicate progress to stakeholders.
- Foster a strong culture of safety and ensure safety practices are integrated into all project activities.
Qualifications:
- Bachelor’s 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
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