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!
Our client is a professional Pharmaceutical organization, based in Basel-Stadt Switzerland.
Our client is a Pharma organization in Basel!
Ensure the implementation of regulatory activities
Compile regulatory files national requirements.
Obtain approval regulatory authorities.
Provides regulatory advice project teams to ensure regulatory concerns
Provide regulatory support to clients associates.
Liaising with regulators
Provide contents review of packaging texts, Summary of Product Characteristics and labelling.
Review for support and to accompany Regulatory Affairs Associates.
Assist for platform / Senior Regulatory Affairs consultants
Provide technical support sales
Ensure technical description of the proposals
Ensure that invoicing is correct
Contribute to the data entry
4 years minimum of professional experience
Expert in regulatory affairs and Swissmedic
You are fluent in English and German
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Daniel Woudenberg.