QA/RA Interim Officer
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 Zuid-Holland Netherlands.
- Provide support for the QA
- Providing product information
- Ensuring that reviews are conducted properly
- Ensuring that the regulatory submissions are followed up and that the system is updated
- Communicate and cooperate with external and internal stakeholders on all levels
- Ability to make priorities
- Bachelor degree
- Experience within a pharmaceutical or biotech industry: 2/5 years minimum
- Experience with European MAAs.
- Experience within regulatory legislation
- Good written and verbal skills in English
The Company
They are one of Europe's leading pharmaceutical and healthcare companies, with headquarters in Italy. The organisation has over forty subsidiaries operating throughout Eastern and Western Europe, with a network of marketing partners covering many other countries throughout the world.Role Description
Working for 2/3 days a week, for a period of 3 months you will be responsible for registration. Giving the essential push to finalise the current key projects.Responsibilities
- Accountable for the registration- Provide support for the QA
- Providing product information
- Ensuring that reviews are conducted properly
- Ensuring that the regulatory submissions are followed up and that the system is updated
- Communicate and cooperate with external and internal stakeholders on all levels
Requirements
- Knowledge of both local and European labelling- Ability to make priorities
- Bachelor degree
- Experience within a pharmaceutical or biotech industry: 2/5 years minimum
- Experience with European MAAs.
- Experience within regulatory legislation
- Good written and verbal skills in English
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