Serialization Reporting and data management support
Location: NetherlandsSIRE® 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!Our client is a professional Pharmaceutical organisation, based in Noord-Brabant Netherlands.
• Respond to customer inquiries on pack status, requests for information and inquiries on serial numbers as well as investigations related to market alert
• Engage in focus groups at European and National level and share learnings in a structured approach
• Support business user readiness including advising and updates to process and procedures (SOP’s) and training
• Support the requirement gathering for the automation of reporting and FMD related processes
• Member of Project Team
– Key contributor to activity planning, resources & skills allocation, day-to-day activity management
• Bsc or Msc degree
• Experience with track and trace related processes in the supply chain
• Experience with testing of SAP enhancements (test scripts execution, defects etc.)
• Experience as trainer for business users
• Excellent in English, both in oral and written communication, additional languages are welcome
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ravi Ramnarain Singh.
The Company
Constant, united and focused is how they describe themselves being one of the early pioneers of biotech. Continuously they strive to serve patients by transforming the promise of science and biotechnology into therapies that have the power to restore health or save lives.Role Description
We are looking for a project subject matter expert who can support the upcoming processes related to the implementation of the EU Falsified Medicine Directive (FMD). This directive is new in the pharmaceutical industry and will require business process changes throughout the supply chain ensuring continuation of products to patients. While the company is preparing we need additional capacity to assist in the ramp-up period.Responsibilities
• Execute manual uploading of masterdata and batch information during the ramp up phase of the project• Respond to customer inquiries on pack status, requests for information and inquiries on serial numbers as well as investigations related to market alert
• Engage in focus groups at European and National level and share learnings in a structured approach
• Support business user readiness including advising and updates to process and procedures (SOP’s) and training
• Support the requirement gathering for the automation of reporting and FMD related processes
• Member of Project Team
– Key contributor to activity planning, resources & skills allocation, day-to-day activity management
Requirements
• Strong knowledge of SAP OTC and PTS /• Bsc or Msc degree
• Experience with track and trace related processes in the supply chain
• Experience with testing of SAP enhancements (test scripts execution, defects etc.)
• Experience as trainer for business users
• Excellent in English, both in oral and written communication, additional languages are welcome
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ravi Ramnarain Singh.
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