Cell Therapy Manufacturing Associate I or II

OrganaBio•San Diego, CA

9h•$27 - $32•Onsite

About The Position

The Cell Therapy Manufacturing Associate I or II is responsible for performing well regulated GMP aseptic cell culture activities including media preparation, cell thaws, cell expansion, cell harvesting, and cryopreservation using standard cell culture technologies in a cleanroom environment. The Associate will be responsible for following Batch Production Records, Standard Operating Procedures, and work instructions in manufacturing spaces. The Associate will be responsible for participating in the maintenance of critical supplies, equipment, product testing, product storage and product distribution.

Requirements

Bachelor’s degree in cell biology or related field with 1+ years industry experience or Associate degree in related area and/or a Biotech Program certificate from an accredited college with 2 + years industry experience.
Strong understanding of aseptic technique and Good Manufacturing Practices (GMP).
Proficient in standard cell culture methods including cell counts using Hemocytometer, perform calculations including cell concentration determination, seeding densities, % viability, weight measurements, and volume.
Interpersonal skills to establish professional relationships both internally and externally.
Critical thinking, creativity, and innovative thinking.
Detail oriented with the ability to set priorities and organize daily work requirements.
Must be able to work both as a team member and independently, as required.
Proficient in professional communication both written and oral, which is clear and precise.
Must keep Management informed on any technical and/or operational issues that arise.
Must be flexible, as production priorities, timelines, and processes can change regularly.
Integrity and discretion – ability to maintain confidentiality.
Ability to perform under pressure and work under stressful situations.

Nice To Haves

Biotech certificate valued, not required

Responsibilities

Experience in aseptic technique, clean room gowning and have knowledge of Good Manufacturing Practices (GMPs).
Documenting of each task, understanding verifier versus operator functions, following cleaning procedures, and ensuring aseptic processing techniques.
Daily updating of Production spreadsheets, review of completed documents, addressing corrections, and communication of document readiness to management.
Responsible for documenting deviations and reporting deviations to department management
Receipt and processing of blood, cord, blood, and tissue collection processes under cGMPs.
Execution of colony forming units assay procedures (CFUs), set up samples for sterility testing, performs flowcytometry assays for viability and cell identification.
Responsible for execution of cell culture manufacturing: cell thawing, cell passaging, cell feeding, harvesting, cell counting, cryopreservation, and stability testing.
Performs sample processing, intermediate formulations, storage, and distribution of product
Operation of supporting equipment for daily manufacturing.
Train on and actively participate in revising of Standard Operating Procedures (SOPs), Batch Production Records (BPRs), Work Instructions, and Forms.
Supports environmental monitoring processes including personnel monitoring, suite monitoring as defined by the facility
Assist with the weekly maintenance/cleaning of equipment and cleanroom to support GMP production.
Assist Subject Matter Expert (SME) with providing training for new and existing employees.
Assist with the ordering, stocking, release of supplies/materials to meet production demands
Provides feedback and support in drafting and implementing documents and procedures for department development/process improvement.
Help identify potential equipment or process issues.
Supports the Excellos safety, GMP and Quality Plan.
Participates in department meetings, proficiency testing, and educational programs.