Validation & Engineering Group
MV01-072825 Project Manager (IN)
Validation & Engineering Group, Indianapolis, Indiana, United States, 46201
Project Manager
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: 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 Partwashers 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 Partwashers. 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: 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 Partwashers. 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
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: 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 Partwashers 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 Partwashers. 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: 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 Partwashers. 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