Kincell Bio collaborates with cell therapy developers by using considerable scientific experience and industry understanding. Backed by North Carolina Biotechnology Center.
About the role
Kincellis Advanced Therapies provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable, federal, state, and local laws. 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.
Essential Duties and Responsibilities
- Utilize proficiency in Microsoft Word, Excel, PowerPoint, and other relevant applications to support manufacturing operations.
- Apply knowledge of aseptic processing, cell culture, and cell therapy manufacturing within a cGMP-regulated environment.
- Maintain strict adherence to personal protective equipment (PPE) requirements to ensure a safe and compliant workspace.
- Collaborate with cross-functional teams to draft, revise, and maintain Standard Operating Procedures...
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