Onsite Contract: Cell Processing Technician (cGMP)

ProKidney; White Settlement (TX); On-site; USD 34,000 - 48,000; Full time

Job summary

ProKidney Corp. seeks a Manufacturing Specialist 1, Cell Processing to support cell processing operations in a cGMP environment. The contractor will set up and operate production equipment, assist in freezing and storage, and ensure accurate GMP documentation in a controlled facility.

Role requires independent work and collaboration with cross-functional teams, adherence to GDP, and meticulous attention to process details in a regulated setting. Onsite in Winston Salem, NC.

Qualifications

• AS/BS in Biotechnology, Biology, Chemistry or related field; relevant experience may substitute.
• 0-2 years in cell processing, biotechnology manufacturing, or related field.
• Strong understanding of cGMP with ability to follow complex protocols.
• Able to work independently or in a team with good record-keeping and time management.

Responsibilities

• Set up and operate production equipment to support cell processing activities.
• Assist in processing, freezing, and storage of biologic products per GDP/cGMP.
• Complete GMP documentation, batch records, logbooks and forms accurately.
• Monitor temperatures, expiry dates, and equipment calibration for products.
• Identify deviations from procedures and take corrective actions.
• Collaborate with cross-functional teams for process improvements and maintenance.
• Conduct aseptic manufacturing in a cleanroom following sterile techniques.

Skills

cGMP knowledge

equipment operation

attention to detail

documentation

time management

teamwork

communication

Education

AS/BS in Biotechnology, Biology, Chemistry

Tools

control rate freezers

orbital shakers

cell processing equipment

Job description

ProKidney Corp. seeks a Manufacturing Specialist 1, Cell Processing to support cell processing operations in a cGMP environment. The contractor will set up and operate production equipment, assist in freezing and storage, and ensure accurate GMP documentation in a controlled facility.

Role requires independent work and collaboration with cross-functional teams, adherence to GDP, and meticulous attention to process details in a regulated setting. Onsite in Winston Salem, NC.