AT01-102725 Packaging Validation Engineer SC
Company: Validation & Engineering Group, Inc
Location: Greenville
Posted on: February 13, 2026
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Job Description:
Job Description 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: Packaging Validation Engineer Location:
Greenville, SC Type: Contract / On-site Summary: We are seeking a
Packaging Validation Engineer with strong leadership and
communication skills to lead packaging qualification and validation
efforts for sterile liquid filling and packaging operations in
Greenville, SC. The selected professional will coordinate and
execute all CQV activities related to a new packaging line handling
liquid products in multiple bottle and cap configurations, working
closely with client engineering, manufacturing, and quality teams
to ensure project success and regulatory compliance.
Responsibilities: Lead the packaging validation project,
coordinating cross-functional efforts and ensuring alignment with
project objectives, timelines, and regulatory requirements. Develop
and execute validation documentation (URS, risk assessments,
FAT/SAT, IQ/OQ/PQ, and final reports) for packaging lines and
related equipment, including fillers, cappers, labelers, conveyors,
vision inspection, and serialization systems. Manage communication
between validation, engineering, and quality teams to drive
efficient decision-making and issue resolution. Oversee
qualification of change parts, line configuration changes, and
multiple bottle/cap presentations. Provide hands-on support during
commissioning and execution phases, including troubleshooting and
deviation resolution. Support process performance qualification
(PPQ) activities and readiness for commercial production. Ensure
all validation deliverables comply with cGMP, FDA, and EU Annex 1
requirements, as well as internal procedures and the site’s
Validation Master Plan (VMP). Qualifications: Bachelor’s degree in
Engineering or Natural Sciences. Experience in packaging validation
for sterile or aseptic liquid operations. Demonstrated experience
leading validation projects or small technical teams. Solid
understanding of liquid filling systems, packaging automation,
inspection technologies, and capping mechanisms. Strong knowledge
of GAMP 5, 21 CFR Part 11, and Annex 1. Excellent communication,
organization, and documentation skills, with the ability to
effectively interact with clients, peers, and management. Ability
to work independently and manage multiple priorities in a
fast-paced, regulated environment. Preferred Skills: Experience
leading packaging validation for sterile liquids or biologics.
Familiarity with serialization and aggregation systems. Previous
client-facing or project leadership experience within
pharmaceutical or biotechnology manufacturing.
Keywords: Validation & Engineering Group, Inc, Rock Hill , AT01-102725 Packaging Validation Engineer SC, Engineering , Greenville, South Carolina
