Cell Therapy Operations Associate

Cell Therapy Operations Associate supporting GMP manufacturing in aseptic cleanroom, Hoofddorp, temporary contract.

Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)

Eisen

  • Comfortable working in full gowning aseptic environments and adhering to strict GMP protocols
  • MLO/MBO/HBO (MBO level or higher) with a background in Life Sciences
  • Knowledge of pharmaceutical manufacturing processes for biotechnology products
  • Experience working in GMP pharmaceutical or biotech manufacturing
  • Skilled in Microsoft Word, Excel, and data analysis tools

Wensen

  • Familiar with cleaning and sterilization procedures such as Vapro A and B or LITOP A and B
Volledige omschrijving

The Company: Our client is a global leader in advanced cell therapy, specializing in developing and delivering cutting-edge treatments for patients with serious illnesses. The organization operates state-of-the-art manufacturing facilities and follows the highest GMP standards to ensure quality and safety.

Role Description: As a Cell Therapy Operations Associate, you are responsible for supporting GMP manufacturing activities within an aseptic cleanroom environment. You will execute production and production-support operations, including material preparation, batch execution, documentation management, and product handling, while ensuring strict compliance with cGMP regulations, SOPs, and quality standards.

Responsibilities: Perform daily operational tasks within the manufacturing process, including the transfer and handling of blood products and cell samples. Support the preparation of growth media and other materials in cleanroom environments. Assist in reviewing batch documentation to ensure accurate and timely product release. Conduct material decontamination and supply manufacturing suites with required components. Prepare, inspect, and cryopreserve final products and excess cells.

Transfer samples to QC for testing and manage sample documentation. Collaborate with the Production Support Team to perform tasks such as apheresis accession and batch transfer.

Requirements: Qualified in MLO, MBO, HBO (MBO level or higher) with a background in Life Sciences. Experience working in GMP pharmaceutical or biotech manufacturing is essential. Knowledge of pharmaceutical manufacturing processes for biotechnology products. Familiar with cleaning and sterilization procedures such as Vapro A and B or LITOP A and B is a plus. Skilled in Microsoft Word, Excel, and data analysis tools. Comfortable working in full gowning aseptic environments and adhering to strict GMP protocols.

Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.

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