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Our client is a pharmaceutical/biotechnology company, based in the Netherlands. The company's mission is to revolutionize human therapeutics by working on genetics technologies and developing medicines to help ill people around the world. The work environment is innovative and high-tech, where your talent and knowledge will be recognized.
Role Description In this role, you will be responsible for quality assurance, you will work with deviations, to resolve technical issues and check for compliance. You will be a facilitator between different departments, making sure that the packaging and labelling of the products are compliant with the SOPs. You will work together with the supply chain, and clinical manufacturing teams, troubleshooting the issues that might appear in the process.
Responsibilities -Manage CAPAs and deviations -Perform checks during production runs -Ensure that the production is conformant with GMP -Create and evaluate SOPs and Work Instructions -Participate in QA production-related projects -Perform batch review support
Requirements -Bachelor’s degree in Chemistry Pharmacy or relevant field. -Min 3 years of QA experience in a pharmaceutical or life science-related industry -Willingness to work in shift. -Knowledge of current GMP regulations. -Good communication.
Other information
Are you interested and do want to apply for this role, please do not hesitate to contact me by applying to this position.
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