Shift Available:
- Sunday–Wednesday (with e/o Wednesday off), Onsite, 11:00 a.m.–11:30 p.m.
Responsibilities:
- Manage material needs/requirements for CAR-T production per SOPs in controlled/classified environments.
- Perform inventory control cycle counts, material stocking, scrapping (at a minimum).
- Manage material expiry, allocation, and maintain material condition requirements.
- Quantify and maintain materials in production dispensary.
- Maintain timing to ensure on-time logistics.
- Record material handling data in a clear format per GDPs; assist with quality investigations as applicable.
- Work in a cross-functional, team-based environment to complete warehousing tasks.
- Adhere to regulatory requirements; must be able to work with blood-derived components.
Knowledge & Skills:
- Knowledge of cGMP/FDA regulated industry; general understanding of cGMPs.
- Basic math; inventory control/management.
- Technical writing capability; proficient in MS Office.
- Background understanding of biology, chemistry, medical/clinical practices.
Basic Requirements:
- Bachelor’s degree with no prior Manufacturing/Operations experience; OR
- Associate/Medical Technical degree with 1–2 years Manufacturing/Operations experience; OR
- High school diploma/GED with 3–4 years Manufacturing/Operations experience.
- Strong attention to detail; strong oral/written communication; strong MS Office experience.
Preferred Requirements:
- 1 year GMP experience; 1 year ERP experience.
Compensation:
- $28.13–$34.09 per hour (Summit West – NJ).
Application instruction:
- Apply even if your resume doesn’t perfectly match; you may be one step away.