UTS- Temporary GMP Manufacturing Technician at UNC Chapel Hill

UTS
- Temporary GMP Manufacturing Technician at UNC Chapel Hill

Please see Special Instructions for more details.

Please include a cover letter, resume and contact information for three professional references.

Posting Number PG195709TM

Position Number 48SM26

Position Type Temporary

The Advanced Cellular Therapeutics (ACT) Facility is a Good Manufacturing Practices (GMP) facility focused on expansion and manipulation of human cells for clinical phase 1 applications, specifically including applications involving chimeric antigen receptor (CAR) T cells. The ACT Facility also manufactures Master Cell Banks (MCBs) used in the production of clinical grade gamma retrovirus vector for use in CAR T clinical trials.

Yes. Appointment Length: 11 months.

As a Pack member,
you belong here
, and can enjoy exclusive perks designed to enhance your personal and professional well‑being. As you consider this opportunity, we encourage you to review our Employee Value Proposition and learn more about what makes NC State the best place to learn and work for everyone.

• Attend non‑revenue generating sporting events for free.

Disclaimer:
Perks and Benefit eligibility is based on Part‑Time or Full‑Time Employment status. Eligibility and Employer Sponsored Plans can be found within each of the links offered.

Job City & State

Department

System Information

Classification

Title:

Temporary‑Service Maintenance

Working Title:

UTS
- Temporary GMP Manufacturing Technician at UNC Chapel Hill

Monday–Friday, 8:00 AM–5:00 PM

Other duties as needed.

• Relevant bachelor’s degree (or foreign degree equivalent) and 3 or more years of relevant experience in substitution.

• Perform cell culture activities within an ISO 7 clean room environment in compliance with Good Manufacturing Practices (GMP).
• Work aseptically in a Biological Safety Cabinet (BSC) to ensure product integrity and prevent contamination.
• Execute cell counting, assess cell viability, and perform related in‑process testing to support the manufacturing of patient‑specific cellular therapy products.
• Follow established Standard Operating Procedures (SOPs) and batch records accurately, documenting all activities in accordance with GMP requirements.
• Make routine manufacturing decisions within defined procedures to support timely and compliant production of patient products.
• Demonstrate sound judgment by recognizing when to seek guidance, elevate issues, or request support from manufacturing leadership or quality personnel when questions or deviations arise.
• Collaborate effectively with cross‑functional teams to ensure safe, consistent, and high‑quality manufacturing operations.

• Assist with maintaining appropriate inventory levels of materials and supplies within clean rooms and controlled release spaces, ensuring proper storage, labeling, and documentation in accordance with GMP requirements.
• Support a variety of manufacturing‑related tasks as needed to meet operational demands, including preparation, cleanup, and coordination of materials and equipment.
• Lead or support validation projects for manufacturing systems, equipment, and processes, including documentation, execution, and data review activities.
• Participate in continuous improvement initiatives to enhance manufacturing efficiency, compliance, and product quality.
• Collaborate with manufacturing, quality, and facilities teams to ensure validated systems remain in a state of control.

NC State University is an equal opportunity employer. All qualified applicants will receive equal opportunities for employment without regard to age, color, disability, gender identity, genetic information, national origin, race, religion, sex (including pregnancy), sexual orientation, and veteran status. The University encourages all qualified applicants, including protected veterans and individuals with disabilities, to apply. Individuals with disabilities requiring disability‑related accommodations in the application…