ATL01-012325 Project Manager - GA
ATL01-012325 Project Manager - GA
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Job Description
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 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 subplans 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 projects 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 .
Qualifications:
Bachelors 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.
Required Experience:
IC
Employment Type
Contract
