Manufacturing Engineer II

Dawar Consulting, Inc.; Santa Monica (CA); On-site; USD 69,000 - 74,000; Full time

Job summary

Manufacturing Engineer II in Santa Monica, CA for a world leader in biotechnology and life sciences. The role focuses on hands-on process development, characterization, technology transfer, and implementation of new cell therapy manufacturing technologies for clinical and commercial use.

The successful candidate will collaborate with Research, Development, Manufacturing, Quality, and Engineering teams to develop robust, scalable, GMP‑compliant cell therapy processes and to apply DOE and

Qualifications

• MS/BS/AS with related engineering background and industry experience.
• Experience in pharmaceutical/biotechnology manufacturing and process development.
• Hands-on experience with automated cell therapy platforms.

Responsibilities

• Design and execute hands-on lab experiments for cell therapy process development.
• Develop and evaluate cell culture processes, materials, technologies, and equipment for GMP manufacturing.
• Perform cell culture and aseptic processing in ISO 5 environment.
• Analyze and trend process and equipment performance; troubleshoot issues.
• Support development and implementation of cell therapy manufacturing equipment and tech transfer.
• Apply DOE and statistical analysis using JMP, Minitab, or similar tools.
• Prepare and review protocols, SOPs, batch records, and regulatory documentation.

Skills

Cell therapy

DOE analysis

Automated platforms

GMP compliance

Bioreactors

Education

MS in Biochemical Engineering

BS in Biotechnology

AS in related discipline

Tools

JMP

Minitab

Single-use systems

Job description

Manufacturing Engineer II

Santa Monica, United States | Posted on 09/11/2026

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 forcell therapy process development, characterization, and optimizationusing 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 anISO 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 ofcell therapy manufacturing equipment, including hardware, software, single‑use systems, and user requirements.
  
• Supporttechnology transfer, scale‑up/scale‑out, process implementation, and GMP manufacturing operations.
  
• ApplyDesign 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 inBiochemical Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology, or a related discipline.
  
• Experience inpharmaceutical/biotechnology manufacturing and process development.
  
• Hands‑on experience withautomated cell therapy platforms.
  
• Strong cell culture and aseptic processing experience in anISO 5 environment.
  
• Practical knowledge ofcGMP manufacturing and pharmaceutical/medical-device regulatory requirements.
  
• Hands‑on process development experience withbioreactors, process monitoring, and DOE/statistical analysis.
  
• Understanding of bioprocess engineering principles includingscale‑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.