ATL04-012325 Commissioning & Qualification (SME) – GA Position Available In Clarke, Georgia
Tallo's Job Summary: Validation & Engineering Group, Inc. is hiring a Commissioning & Qualification Subject Matter Expert (SME) in Athens, GA, offering an estimated salary range of $105K to $153K annually. The role requires a Bachelor's degree, 5 years of engineering laboratory experience, and expertise in project implementation, leadership, and FDA regulations.
Job Description
ATL04-012325
Commissioning & Qualification (SME)•GA Validation & Engineering Group•4.3
Athens, GA Job Details Estimated:
$105K•$153K a year 2 days ago Qualifications CGMP 5 years Engineering Laboratory experience Bachelor’s degree Project implementation Senior level Leadership Communication skills FDA regulations Full 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: Commissioning & Qualification Subject Matter Expert (SME)
Location:
Athens, GA Position Overview:
We are seeking a Subject Matter Expert (SME) to provide specialized knowledge and support for the decommissioning, relocation, commissioning, and qualification of a new QC laboratory. The SME will bring expertise in laboratory systems, utilities, and regulatory compliance to ensure successful project execution.
Responsibilities:
Provide technical expertise in laboratory systems and utilities to support C&Q activities. Collaborate with project teams to ensure alignment with regulatory standards and industry best practices. Conduct risk assessments and develop mitigation strategies for complex technical challenges. Review and approve project documentation, including protocols and reports, for accuracy and compliance. Serve as a resource for troubleshooting and resolving technical issues during the project lifecycle. Provide training and guidance to project team members on specialized topics.
Qualifications:
Bachelor’s degree in engineering, life sciences, or a related field. Minimum of 5 years of experience as a Subject Matter Expert in pharmaceutical or regulated environments. In-depth knowledge of laboratory systems, utilities, and C&Q processes. Strong understanding of cGMP, FDA, and industry guidelines. Excellent problem-solving, communication, and leadership skills.
