Quality Control Analyst III
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 organisation, based in Noord-Holland Netherlands.
• Development, transfer, validation, verification and/or remediation of analytical methods
• Writing of protocols & reports
• Maintain adherence to corporate policies and appropriate regulations through actions and decisions
• Active participation in advanced problem solving, root cause analysis, troubleshooting, interpretation/consultation, verification of quality and test results discussions
• First-line Troubleshooting of laboratory equipment, aides in maintenance and certification of test instruments and apparatus to ensure compliance.
• Active participation in changes or act as change owner as part of continuous improvement.
• A strong analytical oriented mindset.
• Experience with UPLC, CD, PSD, FFF is a preference
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Suleyman Ekiz.
The Company
One of the largest pharmaceutical company's in the world.Role Description
You will be responsible for transfer, validation and verification of analytical methods for testing of new products in the laboratory. Other responsibilities embrace the Method compliancy and lifecycle development and remediation.Responsibilities
• Perform complex testing• Development, transfer, validation, verification and/or remediation of analytical methods
• Writing of protocols & reports
• Maintain adherence to corporate policies and appropriate regulations through actions and decisions
• Active participation in advanced problem solving, root cause analysis, troubleshooting, interpretation/consultation, verification of quality and test results discussions
• First-line Troubleshooting of laboratory equipment, aides in maintenance and certification of test instruments and apparatus to ensure compliance.
• Active participation in changes or act as change owner as part of continuous improvement.
Requirements
• Bachelor degree in analytical chemistry/pharmacy or equivalent experience• A strong analytical oriented mindset.
• Experience with UPLC, CD, PSD, FFF is a preference
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Suleyman Ekiz.
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