GMP Manufacturing Technician

Job Description

Job Summary:

• The Advanced Cellular Therapeutics (ACT) Facility is a Good Manufacturing Practices (GMP) facility focused on expansion and manipulation of human cells for clinical phase 1 applications, specifically including applications involving chimeric antigen receptor (CAR) T cells.
• The ACT Facility also manufactures Master Cell Banks (MCBs) used in the production of clinical grade gamma retrovirus vector for use in CAR T clinical trials.

Duties and Responsibilities:

• Activities include cell culture work within an ISO 7 clean room environment.
• Working aseptically in a Biological Safety cabinet.
• Follow SOPs and execute cell counting, making manufacturing decisions as needed to support patient products being manufactured.
• Know when to ask questions and look for support in manufacturing when questions should arise.
• Helping to maintain inventory stock in clean rooms and release space.
• Supporting variety of other manufacturing duties as they come up as needed.
• Will be required to lead or support projects for validations of manufacturing systems.

Education and Experience:

• Relevant bachelor’s degree (or foreign degree equivalent) and 3 or more years of relevant experience in substitution.