Research Analyst QC
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;
• Knowledge and familiarity with the use of Pharmacopoeia methods;
• A strong analytical oriented mindset;
• Experience with working in a pharmaceutical environment;
• Experience with analytical methods for complex drug products (e.g containing liposomes, proteins, microparticles) is a preference;
• Experience with UPLC, CD, PSD, FFF is a preference;
• Good knowledge of Pharmaceutical quality systems and production processes;
• Team player, but able to work independently without minimal guidance;
• Strong can-do mentality;
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rutger Koning.
The Company
The Quality Control Innovative Laboratory is responsible for transfer, validation and verification of analytical methods for testing of new drug products in the laboratory. Other responsibilities embrace the Method compliance, Life cycle development and remediation.Role Description
The research analyst QC is responsible to develop & validate analytical methods to obtain reliable and robust release testing procedures. Furthermore, the research analyst is involved in non-routine analyses to support investigations as well as the support of submission –related activities for new product introductions into the production department. Taking into account the experience with complex product testing it is considered that the Research analyst Complex drug product may act as key-expert in trouble-shooting analytical challenges with this type of products.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;• Knowledge and familiarity with the use of Pharmacopoeia methods;
• A strong analytical oriented mindset;
• Experience with working in a pharmaceutical environment;
• Experience with analytical methods for complex drug products (e.g containing liposomes, proteins, microparticles) is a preference;
• Experience with UPLC, CD, PSD, FFF is a preference;
• Good knowledge of Pharmaceutical quality systems and production processes;
• Team player, but able to work independently without minimal guidance;
• Strong can-do mentality;
Other information
Temporarily contract till end off the year.Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rutger Koning.
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