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Cell Therapy Specialist Hoofddorp SIRE Life Sciences

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Gevraagd

  • 37 - 40 uur
  • MBO of hoger
  • Engels (taal)

Aanbod

  • Vast contract
 

Vacature in het kort

Hoofddorp
Join a pioneering biopharmaceutical company dedicated to developing cutting-edge cancer immunotherapies. As a Cell Therapy Specialist, you'll play a crucial role in the production and implementation of innovative cell-based treatments. Collaborate with a focused team on GMP runs, contribute to SOP creation, and tackle processing challenges. This role offers a dynamic environment where your expertise in cell therapy will drive impactful advancements in cancer treatment. Continue reading to see why we need your expertise.
 

Over het bedrijf

SIRE Life Sciences
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The Company
Our client is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors.

Role Description
A Cell Therapy Specialist is a professional with expertise in the field of cell therapy, which involves the use of living cells to treat various medical conditions. Their role encompasses a range of responsibilities related to the development, manufacturing, and implementation of cell-based therapies.

Responsibilities
- Execute all responsibilities related to the production of clinical products in accordance with batch records and standard operating procedures (SOPs).
- Collaborate within a small team to conduct Good Manufacturing Practice (GMP) runs closely with Process Development and Quality teams.
- Participate in creating standard operating procedures, batch records, managing deviations, and overseeing change controls.
- Effectively identify and resolve processing and equipment issues.

Requirements
- Graduated in MBO HBO or BSc level as education.
- Experienced in working manufacturing pharmaceutical or biotechnology industries.
- Follow the rules and guidelines SOPs and Clinical Good Manufacturing Practice (cGMP) regulations.
- Having worked with cell therapy products before is an advantage.
- Ability to work in Shifts.

Other Information
Are you interested in this or another role? click the apply button below and I will contact you as soon as possible.

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