SIRE Life Sciences®

MES Specialist (GMP)

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 Biotechnology and Pharmaceutical organization, based in Noord-Brabant Netherlands.

The company you will be working for is one of the largest Biopharmaceutical companies in the world, located in several countries. Their mission is to expand human life expectancy by developing and creating new ways of treatment.

ROLE DESCRIPTION

In this role you will be responsible for supporting manufacturing execution system processes, supporting primary production processes and improve the quality and performance of the production site.

RESPONSIBILITIES

-Systech Guardian Masterdata administration (SKU Setup) and process definition
-MES Batch record administration (parameter value list maintenance)
-Develop and create new MBRs to test new MES/Guardian System Functionality
-Develop testing for new MES and Guardian System Functionality
-Provide MES/Guardian support to Testing for Engineering and Validation teams for development and Qualification testing
-Provide MES/Guardian support to Manufacturing Operations
-Participate and engage with MES Manufacturing Operations team in MBR Design
-Provide training on MES and all its functional aspects to production execution team.

REQUIREMENTS

-At least a Bachelor degree (relevant education) or the equivalent combination of education and experience
-At least 3 years of related experience in an industrial environment
-Good experience in a pharmaceutical / GMP environment
-Knowledge and understanding of Good Manufacturing Practices
-Experience in writing procedures
-Fluent in Dutch and English, both in oral and written communication

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

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SIRE Life Sciences®

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