Manufacturing Engineer II

Job Description
Our client, a world leader in biotechnology and life sciences, is looking for a " Manufacturing Engineer II ".


Location: Santa Monica, CA

Job Duration: 12 Months - Contract To Hire

Rate : $50-$54.50/hr on W2

Company Benefits: Medical, Paid Sick Leave, 401 (k)

This role will focus on hands-on process development, process characterization, technology transfer, and implementation of new technologies for clinical and commercial manufacturing. The successful candidate will work cross-functionally with Research, Development, Manufacturing, Quality, and Engineering teams to develop robust, scalable, and GMP-compliant cell therapy processes.

Key Responsibilities

• Design and execute hands-on laboratory experiments for cell therapy process development, characterization, and optimization using automated platforms.
• Develop and evaluate cell culture processes, materials, technologies, and equipment for introduction into GMP manufacturing.
• Perform cell culture and aseptic processing activities in an ISO 5 environment , including cell passaging, sampling, fluid handling, media preparation, reagent management, and cryopreservation.
• Analyze and trend process and equipment performance; identify opportunities for process improvements and troubleshoot technical issues.
• Support development and implementation of cell therapy manufacturing equipment , including hardware, software, single-use systems, and user requirements.
• Support technology transfer, scale-up/scale-out, process implementation, and GMP manufacturing operations .
• Apply Design of Experiments (DOE) and statistical analysis using JMP, Minitab, or similar tools.
• Prepare and review protocols, SOPs, manufacturing batch records, technical reports, and regulatory-supporting documentation.

Required Qualifications & Experience

• MS with 2+ years, BS with 4+ years, AS with 5+ years, or equivalent experience in Biochemical Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology , or a related discipline.
• Experience in pharmaceutical/biotechnology manufacturing and process development .
• Hands-on experience with automated cell therapy platforms .
• Strong cell culture and aseptic processing experience in an ISO 5 environment .
• Practical knowledge of cGMP manufacturing and pharmaceutical/medical-device regulatory requirements .
• Hands-on process development experience with bioreactors, process monitoring, and DOE/statistical analysis .
• Understanding of bioprocess engineering principles including scale-up/scale-out, hydrodynamics, mass transfer, and bioreactor design

Preferred Qualifications

• Flow cytometry experience.
• mRNA handling and process development experience.
• Experience with automated cell therapy manufacturing platforms.
• Experience supporting technology transfer into GMP manufacturing.
• Experience with JMP, Minitab, or other statistical/process modeling tools.

If interested, please share your updated resume at View email address on click.appcast.io/View email address on click.appcast.io

Skill Set
Cell Therapy, Process Development