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 :
Location : Athens, GA
Position Overview :
We are seeking an experienced Project Manager to oversee the decommissioning, relocation, commissioning, and qualification (C&Q) of a new Quality Control (QC) laboratory. This role will serve as the single point of accountability for project execution, ensuring all deliverables meet client expectations, timelines, and regulatory requirements.
Responsibilities :
Develop the project C&Q master plans, identify task lists and project timelines in line with the objectives and goals of the projects, and propose sub-plans to facilitate the C&Q process, and eliminate roadblocks.Interface with the project teams to develop the overall C&Q phase project plan and schedule, integrating with the project's overall plan. C&Q planned activities include risk assessment, design reviews, test matrices, FATs, SATs, commissioning, installation, operational, and performance verification for all systems as applicable.Lead the C&Q cost and schedule control process.Work closely with Systems' Owners, SMEs, Automation / IT, Quality, and Technology Leads to ensure readiness for facility, process, and clean utilities verification.Manage verification phase improvements, including lessons learned, deviation management, and resolution.Ensure alignment of the C&Q program with corporate standards and engineering best practices.Oversee project C&Q documentation development, management, and quality of turnover documentation packages.Manage the C&Q staffing plan, including hiring, mentoring, and development.Conduct regular meetings and provide updates, progress reports, and metrics to stakeholders.Ensure compliance with GMP, EHS, and client standards during C&Q execution.Qualifications :
Bachelor's degree in engineering, life sciences, or a related field.Minimum of 10 years of project management experience in pharmaceutical, biotech, or regulated environments.Proven experience in laboratory commissioning and qualification projects.Strong understanding of cGMP, FDA, and regulatory requirements.Proficiency with project management tools and software (e.g., MS Project, Excel).PMP certification preferred but not required.Excellent communication, organizational, and leadership skills.
