prokidney
Manufacturing Cell Processing Specialist 1 Contractor
At a Glance
- Location
- Winston-Salem, North Carolina, United States
- Experience
- Up to 2 years
- Posted
- 2026-04-03T13:49:34-04:00
Key Requirements
Domain Knowledge
- Biotech
- Education
- Manufacturing
Requirements
Experience with biologic or cell therapy production is highly desirable.
Strong understanding of cGMP requirements, with proficiency in operating cell processing equipment.
Responsibilities
The Manufacturing Specialist, Cell Processing at ProKidney is responsible for supporting cell processing operations, ensuring compliance with cGMP guidelines in the development and production of regenerative medicine therapies.
This role involves setting up and operating production equipment, including control rate freezers, orbital shakers, and other equipment, while contributing to efficient processing, freezing, and storage of cell therapy products.
Set up and operate production equipment such as control rate freezers, orbital shakers, and other systems to support cell processing activities.
Assist in processing, freezing, and storage of biologic and cell therapy products, ensuring adherence to cGMP standards.
Accurately complete GMP documentation, including batch records, logbooks, and forms, ensuring compliance with Good Documentation Practices (GDP).
Maintain inventory and monitor conditions related to biologic and cell therapy products, including temperature control, expiration dates, and equipment calibration.