Senior Scientist
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.
Innovation is something that you are well known with, applying knowledge of late stage and commercial method validation and filling experience to develop the business. You will lead the analysis of highly complex issues in a technical area and will establish resolutions and decision points in a given program or project. Seeking to improve together with the team in terms of business and work processes, identifying and enabling scientists to cultivate new scientific insights.
Communication overall strategies of projects to others and will act as lead functional and technical member of the project with frequent interaction with internal and external stakeholders.
- Ensure that all necessary procedures are followed and compliance with local and country guidelines and regulations
- Act as the senior author in the preparation of presentations, documents for regulatory filing, patents, scientific publications and journals
- Leading the proper documentation of method validations
- Review and monitor data management processes to ensure that records are properly stored
- Leading the execution of scientific efforts, advance in scientific projects based on results
- Use emerging developments in relevant scientific fields to generate new research ideas and initiatives
- Influence internal collaboration for multi-year projects across several disciplines
- Minimum 10 years' of experience in post-doctoral research
- Minimum of 3 years' of experience in the industrial field
- Expertise in method validation and understanding of analytical quality by design
- Experienced in the following techniques: LC, CE, FFF-MALS, DLS and AUC
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Helene de Vries.
The Company
This company is committed to developing first-in-class or best-in-class vaccines for some of the world's most life-threatening infectious diseases. They have built a dedicated, world-class, multi-functional team across a variety of disciplines to develop a promising vaccines pipeline. In Leiden they have a workforce of 700 scientists and support staff, 45% of their employees have a nationality other than Dutch with over 20 nationalities represented. They partner with many of the world's leading experts, academic and clinical institutions and other pharmaceutical companies for the development of vaccines against, for example: Ebola and HIV.Role Description
You will contribute to defining scientific strategies for late stage programs/technologies and departmental improvements. Creating and managing multiple research plans that will result in the accomplishment of several business objectives. Having indirect or direct people management responsibilities internally and externally or lead as an individual contributor. Typically working under direct supervision with a high level of autonomy and some decision making.Innovation is something that you are well known with, applying knowledge of late stage and commercial method validation and filling experience to develop the business. You will lead the analysis of highly complex issues in a technical area and will establish resolutions and decision points in a given program or project. Seeking to improve together with the team in terms of business and work processes, identifying and enabling scientists to cultivate new scientific insights.
Communication overall strategies of projects to others and will act as lead functional and technical member of the project with frequent interaction with internal and external stakeholders.
Responsibilities
- Direct the implementation of template validation plans and reports- Ensure that all necessary procedures are followed and compliance with local and country guidelines and regulations
- Act as the senior author in the preparation of presentations, documents for regulatory filing, patents, scientific publications and journals
- Leading the proper documentation of method validations
- Review and monitor data management processes to ensure that records are properly stored
- Leading the execution of scientific efforts, advance in scientific projects based on results
- Use emerging developments in relevant scientific fields to generate new research ideas and initiatives
- Influence internal collaboration for multi-year projects across several disciplines
Requirements
- Ph.D. degree in relevant field- Minimum 10 years' of experience in post-doctoral research
- Minimum of 3 years' of experience in the industrial field
- Expertise in method validation and understanding of analytical quality by design
- Experienced in the following techniques: LC, CE, FFF-MALS, DLS and AUC
Other information
You are fluent in English and able to communicate effectively with the site staff, team members and manager.Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Helene de Vries.
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