Regulatory Affairs Manager
Location: NetherlandsSIRE 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-Holland Netherlands.
The company is a fast growing Consumer Health Care Company.
ROLE DESCRIPTION
As a Regulatory Affairs Manager your main focus of this job is to maintain the life cycle management of OTC pharma products. In addition the manager is also involved in the development and registration of new products.
RESPONSIBILITIES
Manager you are responsible and involved in:
- LCM of OTC pharma
- Newly acquired products
- Products from the pipeline
- Strategy of new/old products
- Writing SOPs
- Liaison between the authorities and the company
- Variations in the CMC module 3
- Also able to rewrite parts of this module
- Renewals
REQUIREMENTS
- University degree in a Scientific discipline
- More than 5 years of experience with RA in the pharmaceutical Industry
- Attention to detail
- Hands-on mentality
- Independent
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact .
