Senior Scientist Method Development & Regulatory Filing | Zuid-Holland

Bedrijfsnaam: -
Plaatsingsdatum: 02/07/2019
Standplaats: -


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 and Biotechnology organisation, based in Zuid-Holland Netherlands.The CompanyThey are committed to developing first-in-class or best-in-class vaccines for some of the world’s most life-threatening infectious diseases. 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. At this company, entrepreneurial people are working in a dynamic culture in which innovation and a 'can do' state of mind are the central points.

Role DescriptionImpact
• Contributes to defining scientific strategy for late stage programs/technologies and departmental improvements
• Creates and manages multiple complex research plans that result in the accomplishment of multiple business objectives

People Development/Degree of Supervision
• May have indirect or direct people management responsibility internally and externally (e.g. outsourced, working with external partners, etc.) or lead as an individual contributor
• Typically works under indirect supervision with a high level of autonomy and some decision making
• Applies knowledge of late stage and commercial method validation and filling experience to further develop the business
• Leads the analysis of highly complex issues in a technical area and establishes resolutions/ decision points in a given program/project
• Identifies novel scenarios and nascent scientific/technical opportunities in a specific scientific area
• Seeks to contribute to improving business/work processes to identify and enable scientists to cultivate new scientific insights

Nature of Communication
• Communicates overall strategy of the projects to others
• Acts as lead functional/technical member of the project with frequent interaction with senior internal and external stakeholders

ResponsibilitiesOperations Management
• Directs the implementation of template validation plans and reports
• Ensures that all necessary procedures are followed and compliance with local and country guidelines and regulations for successful method validations

Information Management and Communication
• May act as the senior author in the preparation of presentations, documents for regulatory filing, patents, scientific publications and journals
• Leads the proper documentation of method validations
• Reviews and monitors data management process to ensure that records are properly stored

Program/Project Management
• Leads execution of scientific endeavors and advances scientific projects based on results
• Uses emerging developments in relevant scientific fields to generate new research ideas and initiatives
• Influences internal collaboration for multi-year projects across multiple disciplines

Requirements• Must have Ph.D. degree in relevant scientific field
• Minimum 10 years of post-doctoral experience, of which 3-5 years of business experience performing progressively advanced duties at the Senior Scientist level, or the equivalent training/experience
• Method validation expert and understanding of analytical quality by design
• Experienced in one or more of the following techniques: LC, CE, FFF-MALS, DLS, and AUC
• Interpersonal skills - good command of speaking and writing of country languages and English, ability to communicate effectively with investigational site staff, team members and functional manager.

Other informationPlease submit your application before the 4th of July.

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.




Plaatsingsdatum :
Referentienummer :
Standplaats :
Adres :
Postcode :
9723 HK
Opleidingsniveau :
Uren :
Nader te bepalen
Dienstverband :
Werkervaring :
5 - 10 jaar
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