Manufacturing Technician | Biopharma | Noord-Holland
Location: NetherlandsSIRE® 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.
Due to the nature of the starting material (patient cells) this job requires a high level of proficiency and ownership of the process and media formulation, with the highest skill level of aseptic and sterile techniques.
• 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 the development and optimization of SOPs and batch records;
• Assist in investigations required to manage deviations;
• Assist in managing change controls;
• To successfully troubleshoot processing and equipment issues;
• 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.
• cGMP experience in a pharmaceutical / biotechnology manufacturing environment
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
The Company
They are 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 cell therapies designed to empower the immune system's ability to recognize and kill tumors.Role Description
As Manufacturing Technician you are part of a team in which people of all backgrounds and experiences are respected. Here you work together to save lives and find the cure for cancer. You ensure that all components are adequately supplied and kitted to follow the production schedule along with the formulation and verification of all media lots.Due to the nature of the starting material (patient cells) this job requires a high level of proficiency and ownership of the process and media formulation, with the highest skill level of aseptic and sterile techniques.
Responsibilities
• To perform all tasks associated with the manufacturing of clinical and commercial products following batch records and standard operating procedures (SOPs);• 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 the development and optimization of SOPs and batch records;
• Assist in investigations required to manage deviations;
• Assist in managing change controls;
• To successfully troubleshoot processing and equipment issues;
• 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
• Bachelor’s (University or HBO) or MBO degree• cGMP experience in a pharmaceutical / biotechnology manufacturing environment
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
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