Quality Analyst, Quality Assurance

Responsibilities:

• Review batch records and test results to enable timely lot disposition.
• Track manufacturing, testing, and release activities for clinical batches.
• Coordinate with internal teams and external partners to track batch status.

Qualifications:

• Bachelor’s degree in life sciences or a related field.
• 1–3 years of experience in a Quality or GMP-regulated environment.
• Strong attention to detail and organizational skills.

Environment:

• Fast-paced, mission-driven, small company biotech environment.
• Requires 20%-40% travel.
• Opportunity to work cross-functionally and gain exposure to cell therapy manufacturing.