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Quality Assurance (Entry level)

SIRE Life Sciences®

Netherlands, zagranica

SIRE Life Sciences®

Quality Assurance (Entry level)

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-Brabant Netherlands.

Our client is a professional Pharmaceutical organization with +100 people working on the site located in Noord Brabant. Well-known pharmaceutical company with a large portfolio of medicines from investigational medicinal products to finished dosages.

ROLE DESCRIPTION

The Quality Assurance officer will join a team of 4 Quality employees led by a Senior Quality Assurance Manager. The team will receive the issues or questions originated during the transportation of medicines.
The Quality Assurance Officer will support all the activities related to the maintenance and improvement of the QMS related to non-conformance and CAPA Management.

Duration: initiaal contract for 10 - 11 months (intended to be permanent afterwards.

RESPONSIBILITIES

All activities within Amgen’s quality system associated with the Supply Chain non-conformance investigations, CAPA records
First point of contact for identification and alerting of potential deviations to department standard processes
Investigation of deviations
completion of Class 1 & 2 NC investigation reports
Perform root cause analysis, implementing improvements and corrective actions
Update of procedures, alert stake-holders (internal employees, clients, external partners), documentation and issue report
Develop strong working relationships with International Quality
Compliance of GMP and GDP guidelines

REQUIREMENTS

- Scientific background (Pharmacy, Biology, Chemistry, Bio-chemistry...)
- Ideally basic knowledge of GMP and/or GDP guidelines
- Eagerness to learn
- Good English skills

OTHER

For further information, please contact Patricia Oses on p.oses@sire-search.com or on +31 20 658 98 00.

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

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SIRE Life Sciences®

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