Research Associate III

What you'll do

• Perform aseptic manufacturing, processing, cryopreservation, and shipment of investigational cellular therapy products under cGMP regulations.
• Maintain accurate and contemporaneous Good Documentation Practice (GDP) records for manufacturing, equipment logs, and laboratory activities.
• Execute research and development activities including process optimization and evaluation of new methodologies or technologies.
• Participate in quality control, validation activities, and the facility Environmental Monitoring Program.
• Assist with the preparation, revision, and implementation of Standard Operating Procedures (SOPs) and batch records.
• Manage laboratory operations including inventory, reagent procurement, equipment maintenance, and safety protocol compliance.
• Support Quality Management System activities such as deviation investigations, CAPA, and change controls.
• Record and organize experimental results for the preparation of scientific manuscripts and presentations.

What we're looking for

• Bachelor’s degree in a relevant field required.
• Minimum 5 years of relevant experience required.
• Knowledge of aseptic technique and cell culture principles.
• Knowledge of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
• Proficiency with Microsoft Office, technology, and electronic documentation systems.
• Strong written and verbal communication skills for interacting with colleagues and stakeholders.
• Ability to learn new procedures, technologies, and protocols while adapting to changing priorities.
• Ability to work collaboratively in a team environment and independently following qualifications.