MES Consultant

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.

You will be working within the GMP production environment.

ROLE DESCRIPTION

As the MES Consultant you will be responsible for the analyses of Business / User Requirements and implementations of new MES and ERP modules in a GMP environment. You will work with several business units (IT / Production / Supply Chain) in order to implement and optimize business and production processes.
Therefore we are looking for an experienced MES specialist with strong knowledge of process optimization, GMP validation and implementation projects.

RESPONSIBILITIES

- Improve MES processes in GMP production environment
- Act as the liaison between Operations BU and the SAP Centre of Excellence
- Business and Requirements Analyses of SAP and MES
- Implementation of Serialization processes in the production environment’s ERP platform
- Guarantee GMP Validation of MES and ERP
- Training of End-Users of the Operations and Manufacturing departments
- Implementation of Change Management and CAPAs
- Represent the Manufacturing and Operations BU during audits
- Act as Project Coordinator during implementations and configurations
- Act as subject matter expert in Operations environment and solve complex issues

REQUIREMENTS

- Bachelor’s degree in IT, Engineering or similar
- 5 years’ experience in GMP production environments
- SAP experience
- Knowledge of Continuous Improvement and Lean is a strong plus
- Strong knowledge of Validation / GMP processes
- Fluency in Dutch and English

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