Verista, a leading life sciences solutions provider with 600 experts, is seeking a Senior CQV Engineer / Lead Validation Engineer to join their team in Athens, GA. This role offers an opportunity to work with renowned brands in the life science industry, focusing on solving critical healthcare challenges. The position requires extensive experience in GMP regulated environments, with responsibilities including validation protocol execution, project management, and technical documentation. The ideal candidate will have 6-10+ years of CQV experience, strong communication skills, and expertise in validation processes. Verista offers a comprehensive benefits package, competitive salary range of $87,780-$134,153, and a culture focused on empowerment, client success, and continuous learning. The role combines technical expertise with leadership responsibilities, making it ideal for professionals looking to make a significant impact in the healthcare and biotech sectors. The company's commitment to innovation, professional development, and work-life balance makes this an excellent opportunity for experienced validation engineers seeking career growth.