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Qualified Person Region Amsterdam

SIRE Life Sciences®

Netherlands, zagranica

SIRE Life Sciences®

Qualified Person Region Amsterdam

Location: Netherlands

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!

THE COMPANY

Our client is a professional Pharmaceutical organization, based in Noord-Holland Netherlands.

An international company (CMO) with production sites all over the world.

ROLE DESCRIPTION

You will work for the Quality Operations sub-group of the client which oversees commercial and clinical activities, contract manufacturing operations, supply chain operations and supplier quality functions performed on behalf of the client. You will have primary responsibility for batch disposition activities. The QP is the person responsible for all batch certification and associated responsibilities as detailed in 2001/83/EC as amended.

RESPONSIBILITIES

- Primary responsible for batch disposition activities and for all batch certification and associated responsibilities
- Closely work together with external operations, internal QA Operations, QC, Validation, Compliance, Regulatory and Supply Chain to ensure timely disposition of product
- Responsible for Quality oversight of contact manufacturers, testing and for leading, monitoring and supporting the quality performance of European quality systems according GMP & GDP standards
- Responsible for guarantying that the medicinal products have been manufactured and tested in accordance with GMP and the Marketing Authorization
- Successfully and timely completion of goals and objectives, which will strengthen the international Quality organization
- Responsible for ensuring consistency and communication within Quality department and with key stakeholders

REQUIREMENTS

- Registered Qualified Person
- GMP GDP experience
- Fluent both in Dutch & English
- At least 8 years of experience

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.

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SIRE Life Sciences®

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