ATL01-012325 Project Manager - GA

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

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:

1. 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.

2. 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.

3. Lead the C&Q cost and schedule control process.

4. Work closely with Systems’ Owners, SMEs, Automation/IT, Quality, and Technology Leads to ensure readiness for facility, process, and clean utilities verification.

5. Manage verification phase improvements, including lessons learned, deviation management, and resolution.

6. Ensure alignment of the C&Q program with corporate standards and engineering best practices.

7. Oversee project C&Q documentation development, management, and quality of turnover documentation packages.

8. Manage the C&Q staffing plan, including hiring, mentoring, and development.

9. Conduct regular meetings and provide updates, progress reports, and metrics to stakeholders.

10. 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.