Validation Engineer II

Arrowhead Pharmaceuticals, Inc. is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. The company is seeking a Validation Engineer II to manage and execute commissioning, qualification, and validation (CQV) lifecycle activities supporting internal GMP drug substance manufacturing at the Arrowhead Verona site.

Requirements

• Minimum of 12 years of experience in a validation engineering role
• Bachelor's degree in Engineering or related scientific field
• Thorough understanding of cGMP and FDA requirements
• Strong communication and documentation skills

Benefits

• Competitive salaries
• Excellent benefit package