Associate, QC Analytical, Cell Therapy

About the Role

This role is responsible for supporting Quality Control (QC) testing for in-process, final product, and stability samples. The position may also assist with documentation, deviations, investigations, and continuous improvement efforts.

Schedule: Wed-Sat 6am-4pm

Key Responsibilities

• Perform routine testing of in-process, final product, and stability samples.
• May review GMP documentation and perform data verification.
• Support document revision, project, CAPA, and deviation/investigation related tasks and/or continuous improvement efforts.
• May train analysts on general job duties.
• Perform other tasks as assigned.

Requirements & Tech Stack

• Ability to accurately and completely understand and follow procedures.
• Apply scientific principles to analytical testing and the proper use of laboratory equipment.
• Ability to communicate effectively with peers and management regarding task completion, roadblocks, and needs.
• Attention to detail and demonstrated organizational skills.
• Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
• Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.

Qualifications

• Bachelor's degree preferred in science. An Associate’s degree with an equivalent combination of education and work experience may be considered.
• Netherlands specific: Bachelor's degree /HLO in (bioanalytical) science preferred. MLO level 4 with an equivalent combination of work experience may be considered.
• 0-2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
• Prior experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, aseptic technique) is preferred.