RA Manager
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-Holland Netherlands.
- Organize the preparation, submission and follow-up of authorities (MAA).
- Organize and archives registration files.
- Contributes to process improvements
- Typically resolves problems using existing solutions
- Provide informal guidance to junior staff
- Solves complex problems; takes a new perspective using existing solutions
- Works independently; receives minimal guidance
- Acts as a resource for colleagues with less experience
- Academic working level, minimum of 5 Yrs of related experience.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Windimi Post.
The Company
This is one of the biggest pharmaceutical companies that develops, produces and sells medicines.Role Description
You will lead a small group of experienced RA specialists/associates. Together with the RA Director and the other RA Manager you will be responsible for the strategic planning.Responsibilities
- Plan and manages regulatory activities on both new and in-line products in accordance with health authorities.- Organize the preparation, submission and follow-up of authorities (MAA).
- Organize and archives registration files.
- Contributes to process improvements
- Typically resolves problems using existing solutions
- Provide informal guidance to junior staff
Requirements
- Requires in-depth knowledge and experience of Module 3 variations, incl. eCTD publishing- Solves complex problems; takes a new perspective using existing solutions
- Works independently; receives minimal guidance
- Acts as a resource for colleagues with less experience
- Academic working level, minimum of 5 Yrs of related experience.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Windimi Post.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
Job Description
SIRE® 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-Holland Netherlands.
- Organize the preparation, submission and follow-up of authorities (MAA).
- Organize and archives registration files.
- Contributes to process improvements
- Typically resolves problems using existing solutions
- Provide informal guidance to junior staff
- Solves complex problems; takes a new perspective using existing solutions
- Works independently; receives minimal guidance
- Acts as a resource for colleagues with less experience
- Academic working level, minimum of 5 Yrs of related experience.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Windimi Post.
The Company
This is one of the biggest pharmaceutical companies that develops, produces and sells medicines.Role Description
You will lead a small group of experienced RA specialists/associates. Together with the RA Director and the other RA Manager you will be responsible for the strategic planning.Responsibilities
- Plan and manages regulatory activities on both new and in-line products in accordance with health authorities.- Organize the preparation, submission and follow-up of authorities (MAA).
- Organize and archives registration files.
- Contributes to process improvements
- Typically resolves problems using existing solutions
- Provide informal guidance to junior staff
Requirements
- Requires in-depth knowledge and experience of Module 3 variations, incl. eCTD publishing- Solves complex problems; takes a new perspective using existing solutions
- Works independently; receives minimal guidance
- Acts as a resource for colleagues with less experience
- Academic working level, minimum of 5 Yrs of related experience.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Windimi Post.
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Self employed
- Number of vacancies
- 1
- Min. experience
- Two years
- Min. education
- Bachelor
- Industry / category
- Jobs in Research & Development (R&D)
