TEMP - Sr. Manager quality - Amsterdam - 3 months
SIRE Life Sciences®
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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 organisation, based in Noord-Holland Netherlands.
Role DescriptionYou will be providing support to the Quality Systems and GMDP compliance withing the Quality department. This in order to optimize the global quality proces
Review and approval of internal and external GMDP Deviations and CAPA
Working together with cross functional stakeholders (supply chain, regulatory)
Generation, review and approval of GMDP
Quality/Technical agreements and internal quality agreements
Implementing, maintaining and improving GxP Quality Systems for Europe
Drive improvements to the training system and promote training compliance within SL o Establishment and monitoring of key metrics for quality systems
Ensuring management oversight of the performance of Quality Systems for Europe
Driving compliance within our GxP Quality Systems through effective monitoring and communication
RequirementsA degree in Chemistry is preferred but not essential
A strong background in chemistry/ small molecule GMP is required (technical small molecule GMP input will be required)
At least 5 years of QA experience in the pharmaceutical industry
Proficient in MS Office, MS Excel, MS Access, MS Projects.
Fluency in English
Relevant experience gained within a Pharmaceutical Company
Experience in GxP Quality Systems and GMDP Compliance
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Greg Silberstein.