Regulatory Affairs Consultant
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 Netherlands.
- Plans and manages regulatory activities in accordance with health authorities
- Development and assessment of the documentation database
- Application and implementation of international legislation and documentation
- Provides guidance to junior staff and reviews their work
- Excellent (native) Dutch writing skills
- 5 years of related experience
- Master's degree in pharmacy or related field
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Carla Garcia.
The Company
Our client is a professional Pharmaceutical and Medical Devices organisation, based in Netherlands. Our client is a one of the largest supplier of medicines in the Netherlands, based in Noord-Holland. professional organisation, based in Noord-Holland Netherlands. Our customer is one of the largest supplier of medicines in the Netherlands. Their mission is to improve lives of patience all over the world by delivering innovative and high-quality products.Role Description
In this role you will provide expertise within the RA team for the Module 1.3.Responsibilities
- Support internal stakeholders about RA (specifically module 1.3) related topics- Plans and manages regulatory activities in accordance with health authorities
- Development and assessment of the documentation database
- Application and implementation of international legislation and documentation
- Provides guidance to junior staff and reviews their work
Requirements
- In-depth knowledge and experience of SmPC, PIL, labelling updates including safety variations and artwork review- Excellent (native) Dutch writing skills
- 5 years of related experience
- Master's degree in pharmacy or related field
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Carla Garcia.
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