ProKidney

ProKidney

Manufacturing Cell Processing Specialist 1

Winston-Salem, North Carolina, United States

Work authorization requiredDetected 22 days ago
Process ImprovementGMPCommunicationTime Management

About the role

  • 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.
  • Participate in cell processing activities, ensuring compliance with cGMP guidelines and ProKidney's manufacturing standards.

Responsibilities

  • Set up and operate production equipment such as control rate freezers, orbital shakers, and other systems to support cell processing activities.
  • Maintain inventory and monitor conditions related to biologic and cell therapy products, including temperature control, expiration dates, and equipment calibration.
  • Collaborate with cross-functional teams to support process improvements, troubleshooting, and equipment maintenance.
  • Maintain compliance with all relevant safety policies, rules, and regulations.
  • Perform other duties as assigned.
  • Coordinate with team members and perform tasks with minimal supervision.

Requirements

  • Skills/Abilities: Strong understanding of cGMP requirements, with proficiency in operating cell processing equipment.
  • Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship.
  • Support material qualification, process development, and validation efforts as required.

Nice to have

  • AS/BS in Biotechnology, Biology, Chemistry, or related field
  • a Science-related discipline is preferred.
  • High School Diploma or Equivalent may be considered with significant relevant experience.
  • Preferred minimum 0-2 years of experience in cell processing, biotechnology manufacturing, or a related field.
  • Experience with biologic or cell therapy production is highly desirable.

Skills

  • Strong understanding of cGMP requirements, with proficiency in operating cell processing equipment.
  • Ability to work independently or collaboratively, demonstrate attention to detail, and follow complex protocols.
  • Strong organizational, record-keeping, and time management skills.

Visa & Work Authorization

  • Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship.

This listing is sourced directly from ProKidney's careers page and normalized into a canonical job model.