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Cell Management Specialist
Job in
Morris Plains, Morris County, New Jersey, 07950, USA
Listed on 2026-07-07
Listing for:
Delan Associates, Inc
Full Time
position Listed on 2026-07-07
Job specializations:
-
Manufacturing / Production
Manufacturing & Industrial Operations
Job Description & How to Apply Below
Cell Management Specialist
Location: Morris Plains, NJ.
Shift timings: Tuesday - Saturday, 10 AM : 6:30 PM EST & Sunday to Thursday, 10 AM : 6:30 PM EST.
Job Description SummaryThe Cell Management Specialist is tasked with Apheresis Receipt, Final Product Packaging, Day 0 and Harvest transfers, Inventory Management, and other duties essential to support core functions.
Key Responsibilities- Follow all area governing SOPs, WPs, and batch records with an emphasis on Right First-Time performance
- Ensure prompt and precise data entry
- Maintain compliance with training requirements
- Keep Manufacturing Support areas in an “audit ready” state
- Provide “flow to the work” support when needed/available
- Perform equipment cleaning and maintenance in accordance with governing SOP requirements
- Escalate and help reconcile any observed compliance or safety issues
- Be proficient in various operating systems, such as LIMS, SAP, and MES
- Support monthly and annual cycle counts
- Participate in site/team projects and initiatives
- Act according to Novartis Values and Behaviors
- Ensure accurate SAP/MES inventories for all components
- Properly segregate and store all conditioned materials
- Receive and inspect incoming leukapheresis
- Package and ship final products
- Deliver scheduled Day 0 apheresis for patient processing on time
- The Harvest and storage of final product
- Receive and store final products from scheduled patient processing
- Resolve outstanding issues with internal and external customers through follow-up communication
- Coordinate the shipping, receiving, storage, and processing of goods, possibly including imports/exports
- Verify inventory accuracy of GMP and non-GMP LN2 storage locations
- Ensure availability and accuracy of all materials and documentation to avoid impediments to daily activities
- 1-3 years of related experience in a cGMP/FDA regulated industry; warehouse experience preferred.
- High School diploma required;
Bachelor's degree preferred. - Strong interpersonal, written, and communication skills, along with problem-solving and follow-up abilities.
- Must be well organized, flexible, and able to work with minimal supervision.
- Ability to lift up to 50 lbs., assisted.
- Requires handling chemicals such as corrosives, solvents, and bio-hazardous material.
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