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!Onze klant is een professionele organisatie in Noord-Holland, Netherlands.

The Company

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Role Description

In this role you will be focused on managing and optimizing quality processes. Your main goal will be to make the production sites more efficient and you will also become responsible for the final releases from batches

Responsibilities

Determine policy lines in the quality framework
Act as a QP
Translate the strategies into actual quality projects
Make sure all the required tests are done
Develop and roll out GMP training for staff
Ensure that legal requirements are met
Internal and external audits, including third party facilities

Requirements

A master degree in Life Sciences
QP License
Five years of relevant experience in GMP regulated environment
A proven track-record in auditing third parties
Fluent in both English and Dutch

Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Seppe Verhoeven