Process Engineer II (Cell Culture/Biotech)

Dawar Consulting
  • Santa Monica, California
  • Autofill and Review
30+ days ago

Job Description

Our client, a world leader in life sciences and biotechnology, is looking for a “Process Engineer II” based in Santa Monica, CA.

 

Job Duration: Long Term Contract (Possibility of Conversion to FTE)

Pay Rate : $51.25/hr on W2

 

Company Benefits: Medical, Paid Sick leave, 401K

 

Seeking a Process Engineer II to support the development, optimization, scale-up, and manufacturing of engineered T-cell therapy processes. The role combines hands-on laboratory work with process development, statistical analysis, technical documentation, and cross-functional collaboration supporting INDs, technology transfers, process validation, and GMP manufacturing.

 

Key Responsibilities

  • Conduct hands-on cell culture, aseptic processing, and process development studies.
  • Develop, optimize, characterize, and improve manufacturing processes for T-cell therapies.
  • Design and execute process development studies and DOE/statistical analyses.
  • Analyze and trend process performance and identify improvement opportunities.
  • Support technology transfers, process validation, IND activities, and GMP clinical manufacturing.
  • Develop/review SOPs, study plans, batch records, protocols, and technical reports.
  • Provide process training for GMP clinical production.
  • Collaborate with Research, Translational Medicine, Process Development, Manufacturing, and MSAT teams.
  • Present study results and recommendations to technical and senior leadership.

 

Required Qualifications

  • MS in Biochemical Engineering, Chemical Engineering, or related field + 0 years experience, OR
  • BS in related engineering field + 2 years pharmaceutical manufacturing/process development/technology transfer experience.
  • Hands-on cell culture and aseptic technique experience.
  • Experience with media preparation, cell counting, reagents, and cryopreservation.

Preferred

  • Cell therapy / T-cell manufacturing experience.
  • Knowledge of immunology and T-cell biology.
  • cGMP pharmaceutical manufacturing experience.
  • Process development and DOE experience.
  • Bioreactor experience.
  • JMP or Minitab.
  • Lean Six Sigma, statistical process control, and process data management.

 

 

If interested, please send us your updated resume at

hr@dawarconsulting.com

/

akansha@dawarconsulting.com


 



Numbers & Facts

LocationSanta Monica, California
Websitewww.dawarconsulting.com

Skills

  • Asepsisunmatched
  • Biochemistryunmatched
  • Biologyunmatched
  • Biotech and Pharmaceuticalunmatched
  • Cell Biologyunmatched
  • Cell Culturesunmatched
  • Chemical Engineeringunmatched
  • Clinical Trainingunmatched
  • Cross-Functionalunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Data Managementunmatched
  • Data Processingunmatched
  • Drug Manufacturingunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Immunologyunmatched
  • Laboratoryunmatched
  • Leadershipunmatched
  • Lean Six Sigmaunmatched
  • Manufacturingunmatched
  • Manufacturing/Industrial Processesunmatched
  • Medicineunmatched
  • Minitabunmatched
  • Performance Managementunmatched
  • Process Analysisunmatched
  • Process Developmentunmatched
  • Process Engineeringunmatched
  • Process Improvementunmatched
  • Process Managementunmatched
  • Process Manufacturingunmatched
  • Process Validationunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Statistical Process Controlunmatched
  • Statisticsunmatched
  • Technical Supportunmatched
  • Technical Writingunmatched
  • Training/Teachingunmatched
  • Trend Analysisunmatched
  • United States Department of Energy (DOE)unmatched

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