Job Description & How to Apply Below
Join Amaris Consulting as a Thermal Validation & CQV Engineer in a GMP-regulated workplace. Drive commissioning and qualification activities while ensuring compliance and validation readiness throughout.
As a vital part of our team, you will lead and execute CQV activities for facilities and utilities, focusing on thermal validation. Your expertise in authoring risk-based documentation and thermal validation protocols will ensure efficiency and compliance. Collaborate closely with Operations and Quality teams to achieve successful outcomes and promote a culture of continuous improvement.
Responsibilities Lead CQV activities for facilities and process equipment
Author and review C&Q; documentation and protocols
Plan and perform FAT/SAT and critical test plans
Execute thermal validation using Kaye AVS systems
Validate a variety of sterilization and decontamination systems
Qualifications Bachelor’s degree in Engineering, Pharmaceutical Sciences, or related field
6-10+ years of CQV/thermal validation experience
Solid understanding of GMP compliance and validation principles
Proficiency in Kaye AVS and documentation management tools
Excellent skills in technical writing and analysis
Elevate your career in thermal validation and help ensure our systems meet rigorous standards.
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