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Senior Scientist protein characterisation

Gepubliceerd: ongeveer 2 maanden geleden
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Janssen Vaccines & Prevention is a leading biotechnology company developing vaccines against infectious diseases. LabResource has been elected as their top supplier for the second year in a row and has been contracted to recruit for this position.

Job Description

The main responsibility of the senior Scientist is to guarantee the correct design and execution of experiments for the development and validation of protein characterisation techniques .

Typical characterisation techniques include LC, CE, FFF-MALS, DLS, and AUC

His/her activities must be executed, documented and reported according to Good Clinical Laboratory Practice (GCLP) quality requirements.

  • 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
  • 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
  • Acts as lead functional/technical member of the project with frequent interaction with senior internal and external stakeholders

Job Requirements

For this position we are recruiting laboratory professional with the following background:

  • PhD in biochemiscal / analytical or relevant scientific field
  • 2-3 years of industry experience in Method Development & Regulatory filing
  • Affinity for data analysis and the thorough review of the data generated by others
  • Method validation expert and understanding of analytical quality by design
  • xperienced in one or more of the following techniques: LC, CE, FFF-MALS, DLS, and AUC
  • Experience with experimental plans using the “Design of Experiment (DoE)” principles is a plus
  • Excellent communication skills, fluent in English.
  • Experienced in working under quality standards such as GLP, or GMP.
  • Candidates without a valid work permit are not considered for this position.

Salary and Benefits

Contract: 1 year, realistic long term perspectives

Salary: ranging from 4500- 6200 gross monthly

Hours: 32-40

Region: Leiden

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