UTS - Temporary GMP Manufacturing Technician at UNC Chapel Hill

UTS - Temporary GMP Manufacturing Technician at UNC Chapel Hill

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Please see Special Instructions for more details.

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

Posting Details

Position Information

Posting Number - PG196048TM

Position Number - 48LS99

Position Type - Temporary

Essential Job Duties - 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 CART clinical trials.

Is Time Limited - Yes

If Yes, Appointment Length - 11 months

Wolfpack Perks and Benefits - 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.

What we offer:

Health Insurance for Temporary Employees

Enhance your career with LEAD courses

Attend non-revenue generating sporting events for free.

Attain work-life balance with our Childcare discounts, Wellness & Recreation Membership, and Wellness Programs that aim to build a thriving wolfpack community.

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.

Department Information

Job City & State - Chapel Hill, NC

Department

System Information

Classification Title - Temporary-Service Maintenance

Working Title - UTS - Temporary GMP Manufacturing Technician at UNC Chapel Hill

Position Information

Requirements and Preferences

Work Schedule - MondayFriday, 8:00 AM5:00 PM

Other Work/Responsibilities - Other duties as needed

Minimum Experience/Education - Relevant bachelor's degree (or foreign degree equivalent) and 3 or more years of relevant experience in substitution.

Department Required Skills - Perform cell culture activities within an ISO7 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, escalate 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.

Preferred Years Experience, Skills, Training, Education - 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.

Required License or Certification - N/A

Valid NC Driver's License required? - No

Commercial Driver's License Required? - No

Recruitment

Recruitment Details

Anticipated Hiring Range - $31.25/hourly

Recruitment Dates

Job Open Date - 06/09/2026

Applicant Information

EEO - 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 and interview process are welcome to contact View phone number on click.appcast.io to speak with a representative of the Office of Equal Opportunity. If you have general questions about the application process, you may contact Human Resources at View phone number on click.appcast.io or View email address on click.appcast.io. Final candidates are subject to criminal & sex offender background checks. Some vacancies also require credit or motor vehicle checks. Degree(s) must be obtained prior to start date in order to meet qualifications and receive credit. NC State University participates in E-Verify. Federal law requires all employers to verify the identity and employment eligibility of all persons hired to work in the United States.

Supplemental Questions

Required fields are indicated with an asterisk (*).

1. * How did you hear about UTS?

   (Open Ended Question)

2. * Do you have direct experience performing aseptic cell culturespecifically with CAR-T cells or viral vectorswithin an ISO 7 cleanroom environment?
   • Yes
   • No
3. * What is your experience executing Batch Records and making real-time manufacturing decisions, such as adjusting a process or seeking support based on cell count and viability data?

   (Open Ended Question)

4. * Can you describe your experience leading or supporting validation projects (such as IQ/OQ/PQ) for equipment or manufacturing systems in a clinical facility

   (Open Ended Question)

Applicant Documents

Required Documents

1. Resume
2. Contact Information for References

Optional Documents

1. Cover Letter

North Carolina State University