Immediate need for a talented
Process Engineer – Cell Therapy. This is a
06+months contract opportunity with long-term potential and is located in
Los Angeles, CA(Onsite). Please review the job description below and contact me ASAP if you are interested.
Job ID:26-30031
Pay Range: $46 - $51/hour. Traveler benefits as per agency package. (Benefits vary by vendor and assignment.).
Key Responsibilities:- Perform hands-on laboratory work supporting cell therapy process development, optimization, characterization, and continuous improvement.
- Develop, evaluate, and optimize manufacturing processes for engineered T-cell therapy products.
- Design and execute process development studies to establish an understanding of critical operating and process performance parameters.
- Support process development activities associated with new INDs, technology transfers, process validation, and GMP manufacturing.
- Perform cell culture and aseptic processing activities, including:
- Cell culture
- Media preparation
- Cell counting
- Reagent preparation and management
- Cryopreservation
- Analyze process data and trend process performance to identify process improvements and opportunities for optimization.
- Apply Design of Experiments (DOE) and statistical analysis to process development studies.
- Support process training for GMP clinical manufacturing personnel.
- Participate in cross-functional CMC development activities.
- Prepare and review technical documentation, including SOPs, study plans, process protocols, manufacturing batch records, technical reports, and summary reports.
- Develop presentations and data summaries to communicate technical results to senior leadership and cross-functional teams.
- Troubleshoot process issues and apply structured problem-solving techniques.
- Collaborate with Research, Translational Medicine, Process Development, Manufacturing, and MSAT teams.
- Support additional process development and cross-functional activities as required.
Key Requirements and Technology Experience:- MS Degree: Biochemical Engineering, Chemical Engineering, Bioengineering, or related discipline with 0+ years of relevant pharmaceutical manufacturing, technology transfer, or process development experience.
- BS Degree: Biochemical Engineering, Chemical Engineering, Bioengineering, or related discipline with 2+ years of relevant pharmaceutical manufacturing, technology transfer, or process development experience.
- Hands-on cell culture experience.
- Strong aseptic technique experience.
- Experience with media preparation, cell counting, reagent management, and cryopreservation.
- Process development or process engineering experience within pharmaceutical, biotechnology, biologics, or cell therapy environments.
- Strong troubleshooting and problem-solving abilities.
- Ability to analyze process data and identify trends.
- Excellent written and verbal communication skills.
- Ability to work independently with minimal direction.
- Ability to manage multiple priorities in a fast-paced environment.
- Strong collaboration skills within cross-functional technical teams.
- Cell therapy or T-cell process development experience.
- Knowledge of immunology and T-cell biology.
- GMP manufacturing experience.
- Technology transfer and/or process validation experience.
- Experience with Design of Experiments (DOE).
- Experience with bioreactors.
- Experience with JMP or Minitab.
- Knowledge of Statistical Process Control (SPC).
- Knowledge of data management and statistical process analysis.
- Lean Six Sigma knowledge.
- Experience supporting CMC activities, clinical manufacturing, or IND-related process developmen
Our client is a leading
Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
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