Biomanufacturing Associate II

Responsibilities

• Perform routine right-first-time cGMP manufacturing of cell and gene therapy products including aseptic processing, cell isolation, culturing, and cryopreservation
• Execute upstream and downstream processing, aseptic fill finish, and final product visual inspection
• Review and author SOPs, batch records, and manage material ordering
• Provide input for equipment selection, process design, and material flows
• Work with Quality Assurance and MSAT to resolve deviations, CAPAs, and Change Controls
• Collaborate with cross-functional teams including process development, facilities, and quality control
• Identify opportunities for improvements in safety, quality, delivery, and cost

Requirements

• Bachelor’s degree in biological sciences or related engineering
• 2-4 years of experience in cGMP biotech manufacturing
• Proficiency in aseptic technique and/or processing
• Strong communication skills and proficiency in Microsoft Office
• Ability to function in a dynamic environment and balance multiple priorities

Preferred Qualifications

• Experience with cGMP manufacture or process development for CAR T, TCR, TIL, or mRNA
• Experience with primary cell culture and equipment such as BSC, CliniMACS, LOVO, or G-Rex systems

About the Company

ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization through integrated technologies and manufacturing expertise.