QC & Lab Manager
Location: United KingdomSIRE® 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 Medical Devices and Biotechnology organisation, based in Surrey United Kingdom.
• Responsible for biological and quality controls
• Participate in CAPA process and meetings
• Follow up of QA activities with suppliers
• Responsible for biological and particular controls in the cleanroom
• Plan Bioburden and LAL validations as well as bio compatibility studies
• Participate in internal and external audits
• Assist the Quality Manager in the maintenance and application of the Quality Manual
• Sound medical devices standard and processes knowledge (QSR, ISO 13485)
• University degree or equivalent
• Experience and knowledge in Microbiology
• Knowledge of 3D measuring devices desired
• Excellent organisational skills
• Responsible, precise, rigorous and a team player
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Riko Arends.
The Company
Our client is a international biomedical device company located in SurreyRole Description
QC & Lab ManagerResponsibilities
• Manage the UK laboratories with 2 direct reports• Responsible for biological and quality controls
• Participate in CAPA process and meetings
• Follow up of QA activities with suppliers
• Responsible for biological and particular controls in the cleanroom
• Plan Bioburden and LAL validations as well as bio compatibility studies
• Participate in internal and external audits
• Assist the Quality Manager in the maintenance and application of the Quality Manual
Requirements
• 5 years’ of relevant experience in the biomedical and quality assurance field• Sound medical devices standard and processes knowledge (QSR, ISO 13485)
• University degree or equivalent
• Experience and knowledge in Microbiology
• Knowledge of 3D measuring devices desired
• Excellent organisational skills
• Responsible, precise, rigorous and a team player
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Riko Arends.
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