GMP Biotech Technician — Cell Therapy Manufacturing

Cedars-Sinai; West Hollywood (CA); On-site; USD 60,000 - 90,000; Full time

Job summary

Cedars-Sinai seeks a Biomedical Technician to support wet- and dry-lab projects in the CBC. You will perform process development tasks, maintain equipment, and ensure documentation per SOPs and regulatory guidelines.

Responsibilities include sample verification, inventory management, and collaboration with cross-functional teams to troubleshoot and address issues in a GMP-like environment. A biology/biochem background is preferred.

Qualifications

• 1 year of lab/biotech experience required.
• Must be able to document in lab notebooks, SOPs and batch records.
• Knowledge of regulatory requirements (FDA, Federal, State).
• Familiar with routine lab procedures and experimental protocols.

Responsibilities

• Performs process development tasks for multiple clients following SOPs; tasks vary by project.
• Writes and maintains documentation in lab notebooks, data records, SOPs, and batch records.
• Drafts SOPs and maintains the computer database.
• Verifies samples, logs them into systems, and may transport to storage per SOPs.
• Performs lab maintenance, including glassware cleaning and sterilization.
• Maintains lab equipment and related records.
• Prepares and maintains material inventories; places orders for equipment.
• Assists in operating specialized equipment and machinery.
• Ensures activities comply with regulatory guidelines and safety standards.
• Interacts with core lab customers professionally and communicates clearly.

Skills

Lab experience

Biomedical equipment maintenance

Interpersonal/communication

Regulatory knowledge

Computer skills (Excel/Word/PowerPoint

Documentation (notebooks/SOPs)

Education

Assoc. degree/College diploma in biology/biochemistry or related field

Bachelor's degree preferred

Tools

Laboratory equipment

Job description

Cedars-Sinai seeks a Biomedical Technician to support wet- and dry-lab projects in the CBC. You will perform process development tasks, maintain equipment, and ensure documentation per SOPs and regulatory guidelines.

Responsibilities include sample verification, inventory management, and collaboration with cross-functional teams to troubleshoot and address issues in a GMP-like environment. A biology/biochem background is preferred.