Manufacturing Associate

Responsibilities:

• Perform and verify manufacturing tasks per batch records and SOPs.
• Collaborate with Materials Management, Quality Control, and Quality Assurance for GMP runs.
• Set up, operate, clean, and maintain routine equipment.
• Draft and revise batch records and SOPs for process improvements and GMP compliance.
• Work in a cleanroom environment with gowning requirements.
• Report and troubleshoot processing and equipment issues.
• Participate in technology transfers with internal groups.
• Complete training for technical skills and cGMP compliance.
• Maintain cleanroom material and supply inventories.
• Perform other assigned duties.

Qualifications:

• Bachelor's degree in biology or related field with 1-2 years of cGMP experience, or an associate degree with 3-4 years of cGMP experience.
• Experience with aseptic techniques and cell culture, especially T cells, preferred.
• Strict adherence to SOPs and cGMP regulations with accurate documentation.
• Proficiency with Microsoft Office.
• Ambitious and open to temporary assignments.