Jobs at VaLogic Bio LLC

Performs inspection, certification, repair, and testing of HEPA filters and cleanroom devices at customer sites. Records test data, maintains tools/equipment, follows contamination control and cleanroom practices, and may perform NSF/EM/compressed air testing after training.

The CQV Engineer will lead validation efforts, develop documentation, conduct field verifications, and ensure compliance with cGMP regulations across multiple client sites, supporting the delivery of life-saving therapies.

Travel to client sites to perform hands-on calibration, troubleshooting, repair, and documentation of dimensional, electrical, electronic, electro-mechanical, and mechanical test equipment in GMP-regulated pharmaceutical and biotech environments. Maintain procedures and records, support audits, resolve equipment malfunctions, and provide technical customer support while growing internal calibration capabilities.

Drive growth by identifying and qualifying new business opportunities, maintaining client relationships, developing sales strategies, collaborating with sales and design teams, and training junior sellers. Conduct market research, present proposals, and ensure sales and profit goals are met while representing company products and competitive position.