Cell Therapy Manufacturing Associate

Role Overview

We are currently looking for a Cell Therapy Manufacturing Associate to join a rapidly expanding cell therapy company based in the Hertfordshire area. As the Cell Therapy Manufacturing Associate you will be responsible for manufacturing genetically engineered T cell products. This is a great opportunity for a graduate that has experience working in GMP or a Scientist with extensive experience with T-Cells.

Key Duties and Responsibilities

Your duties as the Cell Therapy Manufacturing Associate will be varied however the key duties and responsibilities are as follows:

1. Carry out work within a GMP manufacturing facility, ensuring FDA, EU and MHRA guidelines are met.

2. You will work in a cleanroom environment with core manufacturing teams and complete documentation.

3. Work alongside the Manufacturing Scientists and Quality Control Teams to establish an engineered T cell manufacturing program and implement the manufacturing processes into the facility.

4. It will be your responsibility to prepare, review and revise SOPs and manufacturing reports.

Role Requirements

To be successful in your application to this exciting opportunity as the Cell Therapy Manufacturing Associate we are looking to identify the following on your profile and past history:

1. Relevant BSc, MSC or PhD in a Biological Science or similar discipline along with progressive industry experience.

2. Proven industry experience in Cell Therapy manufacturing is strongly preferred however a strong immunology background will also be considered.

3. Knowledge and practical experience working within a GMP regulated facility is essential to your application.

Key Words: Cell Therapy | Cell Culture | Manufacturing | T-Cell | CAR T-Cell | Stem Cell | GMP | Biopharma | Cleanroom | GMP | Cell and Gene Therapy | USP | DSP | Upstream | Downstream | Hertfordshire