Qualified Person
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 Flevoland Netherlands.
- Investigate Product Quality and/or Compliance issues/deviations
- Support the lead with the development, negotiation and maintenance of up to date Quality Agreements with GMP/GDP contractors involved in manufacture, relabeling & repackaging, laboratory testing or activities at Logistics Service Providers
- Support the Lead in the preparation and coordination of Regulatory Agency and internal inspections of Product Quality and Compliance (GMP/GDP) activities
- Experience in GMP & GDP
- Qualified Person in the Netherlands
- Dutch and English verbal and written
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
The Company
They are part of a Fortune 500 company.Role Description
Responsible as QP for 1 day per weekResponsibilities
- Manage (deploy, update and maintain) an effective and sustainable Quality System- Investigate Product Quality and/or Compliance issues/deviations
- Support the lead with the development, negotiation and maintenance of up to date Quality Agreements with GMP/GDP contractors involved in manufacture, relabeling & repackaging, laboratory testing or activities at Logistics Service Providers
- Support the Lead in the preparation and coordination of Regulatory Agency and internal inspections of Product Quality and Compliance (GMP/GDP) activities
Requirements
- Master Degree in Pharmaceutical Sciences- Experience in GMP & GDP
- Qualified Person in the Netherlands
- Dutch and English verbal and written
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.
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