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SIRE Life Sciences® / Oferta z dnia: 2020-11-21

Oferowana praca

Miejsce pracy: zagranica
Branża: Projektowanie / Inżynieria

Opis stanowiska

SIRE® 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 Slough United Kingdom.The CompanyOur client is a Pharmaceutical company in the Slough areaRole DescriptionThe QA Incident Manager is the contact persons for the specialist departments and advises proactively on the conduct of the investigations as well as on the preparation of the investigation reports and the definition of measures.Furthermore, the tasks include the creation, testing and approval of work instructions (SOPs). On the one hand, as an author and, on the other hand, as an auditor and approver, you coordinate the tasks of creating and approving SOPs across all departments.The QA Incident Manager will also assist the group in the preparation and implementation of GMP training and administrative activities.Responsibilities- Collect, process and approve complaints (Customer complaints),- The examination and the decision of deviations from the Quality assurance system,- The coordination and execution of defect investigations,- The review and approval of investigation reports of quality assurance events- The definition of corrective and preventive measures (CAPA)Requirements- Master in science, preferably with chemical, pharmaceutical or process engineering orientation- First professional experience in the GMP environment- You enjoys a careful and result-oriented way of working and enjoys documenting- Practical experience in quality assuranceAre 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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