Specialist III, QA Operations (Contract)

Adverum Biotechnologies is seeking a Specialist III, QA Operations (Contract) to lead and execute quality assurance activities for the disposition of cell and viral banks/drug substance/drug product lots, ensuring accuracy, completeness, and compliance with cGMP, regulatory requirements, and company quality standards.

Requirements

• Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Pharmacy) or equivalent experience
• Minimum 5 years of experience in Quality Assurance within the pharmaceutical, biotechnology, or related regulated industry, including experience with lot disposition
• Experience working with CMOs and CTLs in a cGMP environment preferred
• Strong understanding of cGMP, ICH guidelines, and applicable regulatory requirements
• Proficient in reviewing manufacturing batch records, analytical data, and quality documentation
• Excellent attention to detail and ability to make sound quality decisions
• Strong organizational, problem-solving, and communication skills
• Ability to work independently and in a cross-functional team environment
• Proficiency with electronic quality management systems (e.g., MasterControl) is an asset

Benefits

• $50 - $60 an hour