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Associate I, Manufacturing - Temporary Worker

Kincell Bio · Gainesville, FL · On-site

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About Kincell Bio

Kincell Bio collaborates with cell therapy developers by using considerable scientific experience and industry understanding. Backed by North Carolina Biotechnology Center.

About the role

As a Contingent Manufacturing Associate I, you will be responsible for operating both automated and manual cell therapy equipment of varying complexity to support CAR-T, CAR-M, or CAR-NK manufacturing processes, following established standard operating procedures and company policies. You will conduct quality control analyses to support in-process batch production and detect any process deviations. Found on 1752vc Careers, the job board for startup and VC roles.

What they're looking for

  • High school diploma or equivalent required, 0–2 years of relevant education and/or experience in a related field
  • Ability to work 40 hours per week, including weekends as needed
  • Ability to work independently and maintain focus in a fast-paced environment
  • Strong attention to detail, with the ability to recognize deviations in processes, procedures, equipment, materials, and products
  • Effective verbal communication skills
  • Proven ability to work collaboratively within a team-oriented environment
More about this role

Kincellis Advanced Therapies is a U.S.-based contract development and manufacturing organization supporting advanced-therapy developers from early-stage CMC, process and analytical development through clinical supply, pivotal-stage programs and commercial supply. With facilities in Gainesville, Florida; Research Triangle Park, North Carolina; and The Woodlands, Texas, Kincellis combines broad technical expertise with flexible, scalable GMP infrastructure across autologous and allogeneic therapies, including but not limited to CAR-T, Tregs, CAR-NK, MSCs, dendritic cell vaccines, exosomes, iPSCs & synthetic mRNA.

For more information, visit our website at www.kincellis.com.

As a Contingent Manufacturing Associate I, you will be responsible for operating both automated and manual cell therapy equipment of varying complexity to support CAR-T, CAR-M, or CAR-NK manufacturing processes, following established standard operating procedures and company policies. You will conduct quality control analyses to support in-process batch production and detect any process deviations. This role involves handling leukapheresis-derived cellular materials; therefore, you will receive comprehensive...

Read the full posting on Kincell Bio's site ↗

Manufacturing

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