Engineer I, Process Validation

Arrowhead Pharmaceuticals, Inc. is a clinical stage biopharmaceutical company developing medicines that treat intractable diseases by silencing the genes that cause them.

Requirements

• BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry.
• 8 years of experience in GMP validation or a related field.
• Knowledge of process and cleaning validation activities, including test methods, execution, and data analysis.
• Excellent technical writing skills with high attention to detail.
• Excellent problem-solving skills and attention to detail.
• Strong written and verbal communication skills to effectively interact with internal teams, management, and regulatory bodies.
• Experience with regulatory submissions and/or inspections.
• Ability to work across teams.
• Experience in drafting and reviewing validation protocols and reports.
• Strong understanding of GMP regulations, validation principles, and industry best practices.
• Experience in a pharmaceutical or biopharmaceutical manufacturing environment.

Benefits

• Competitive salary
• Excellent benefit package