• Develop a comprehensive understanding of and be able to proficiently execute current cell therapy manufacturing process.
• Complete training sessions and ensure training documentation is maintained.
• Understands and complies with quality standards and requirements as documented.
• Provides operational support functions including materials stocking, kit preparation, reagent preparation, cleaning activities, and equipment maintenance.
• Supports technical transfer and additional research level testing activities.
• Adheres to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs), including Good Documentation Practices (GDP). Completes recording of data to comply with regulatory requirements.
• Support documentation needs, which may include drafting and approval of SOPs, Batch Records, Deviations, CAPAs, etc. Perform basic revisions as needed to accurately reflect current procedures.
• Attends the daily lab meeting and escalates issues/concerns at that forum to Area Management for further investigation.

Job Types: Full-time, Contract

Pay: From $22.00 per hour

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday
• Night shift

Education:

• Bachelor's (Preferred)

Experience:

• Clinical research: 1 year (Preferred)
• Cell culture: 1 year (Preferred)
• Mammalian cell culture: 1 year (Preferred)
• GMP: 1 year (Preferred)

Work Location: In person