avidbio
The Validation Engineer I supports commissioning, qualification, and validation activities for GMP equipment, utilities, facilities, and computerized systems within a biopharmaceutical manufacturing environment. This role involves developing and executing validation protocols, reviewing technical documentation, and ensuring compliance with regulatory standards and company procedures. The position requires cross-functional collaboration to maintain the validated state of GMP systems and support quality assurance initiatives.
Headquarters
Tustin, California, United States
Company Size
201-500 employees
Founded
2002
Avid Bioservices is a contract development and manufacturing organization (CDMO) specializing in mammalian protein development and manufacturing for the biotechnology and biopharmaceutical industries. With over 30 years of experience, they provide process development and cGMP clinical and commercial manufacturing services, supporting programs from early-phase development through commercial-scale production. Avid is known for its world-class facilities, exceptional quality standards, and personalized approach to helping sponsors bring biologics to market faster and at lower cost.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for avidbio.
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