Cell Therapy Specialist | dagploeg | Noord-Holland

Location: Netherlands

SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical and Biotechnology organisation, based in Noord-Holland Netherlands.

The Company

They are at the forefront of cancer immunotherapy. Today, they are a leader in engineered T cell therapy, transforming cancer treatment with what is potentially the biggest breakthrough since the introduction of combination chemotherapy. To bring about this transformation, they are developing innovative products that harness a patient's own immune system to target and attack cancer cells.

Role Description

We are seeking a highly motivated individual to be part of a team that works on innovative T cell therapy for cancer treatment. You will be responsible for media preparation, material staging, waste handling, sample delivery, visual inspection/cryopreservation of drug product in a cGMP manufacturing facility.

In this role, you will ensure that all components are adequately supplied to follow the production schedule, and due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process.

You will be working in a brand new state-of-the-art manufacturing plant.

Responsibilities

• To perform tasks associated with the manufacturing of clinical and commercial products following batch records and standard operating procedures (SOPs) in B, D and CNC grade areas;
• To work as part of a dedicated and committed team to execute GMP runs in close collaboration with Product Sciences, Material Management, and Quality Assurance & Quality Control;
• To assist in optimization of SOPs and Batch records, revise existing Manufacturing Batch Records, SOPs, WIs to support process improvements and maintain GMP compliance;
• Assist in investigations required to manage deviations;
• Assist in managing change controls;
• To strictly comply with SOPs and cGMP regulations; accurately complete documentation associated with clinical and commercial manufacturing;
• To ensure a consistent process execution to guarantee high quality output;
• To maintain cleanroom in an optimal state;
• To continuously look for improvements to the processes to increase quality and efficiency.

Requirements

- MBO/HBO Level with a minimum of 2 years of cGMP experience in a pharmaceutical / biotechnology manufacturing environment;
- Cell culture processing experience is a strong plus;
- Experience with aseptic processing is a strong plus;
- English communication skills are a strong plus.
- Have the ability to lift over 14 Kgs.

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