What are the responsibilities and job description for the Validation Engineer position at SRG?
The QC Laboratory Equipment Qualification Specialist/Validation Engineer supports quality control operations by executing laboratory equipment qualification activities in compliance with cGMP requirements and internal quality standards. Under direct supervision, this role ensures laboratory equipment is qualified, compliant, and fit for intended use through protocol execution, documentation, and coordination with laboratory staff, vendors, and internal support teams.
The position contributes to regulatory readiness, operational reliability, and continuous improvement by identifying compliance gaps, maintaining accurate records, and supporting efficient, compliant laboratory operations within a regulated environment.
Requirements
Equipment Qualification & Validation Expertise
- Ability to execute laboratory equipment qualification activities (IQ/OQ/PQ or equivalent) in accordance with established procedures and regulatory expectations.
cGMP Knowledge
- Strong working knowledge of cGMP regulations and quality systems as applied to QC laboratories and regulated environments.
Technical Documentation Proficiency
- Skilled in authoring, reviewing, and executing qualification protocols and reports with clear, accurate, and compliant documentation practices.
Analytical Laboratory Awareness
- Understanding of QC laboratory operations and analytical equipment to ensure qualification aligns with intended use.
Experience Level
Minimum of two years experience in Validation or equipment qualification is desired.