Bloomington CQV/CSV Validation Engineers

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do the right thing
• We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
• We constantly acquire new skills and learn from our experiences to enhance our collective expertise

Are you a skilled Validation Engineer with a passion for ensuring quality in the pharmaceutical industry? Verista is actively seeking talented professionals to join our team in the vibrant Bloomington, IN area!

Who We’re Looking For:

• Experience: 3+ years in validation engineering within pharmaceuticals or biotech.

• Skills: Expertise in equipment qualification, Delta V, Upstream/Downstream process validation, GMP compliance, CIP/SIP, HVAC, or Utilities.

• Location: Based in or willing to relocate to Bloomington, IN.

• Passion: Dedicated to delivering high-quality solutions that ensure patient safety and regulatory compliance.