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Scientist Vaccine Stability Studies (CMC, pharma)

We are looking for a scientist with experience in a GMP or QC pharmaceutical setting. In this role you will be working on a phase 3 project that will go commercial within the analytical development team.

Job Description

For our pharmaceutical client we are looking for an experienced scientist who will play a key role within the analytical development quality team.You will be involved in the design, execution and evaluation of stability profiles for novel vaccines. Additionally the team also supports the clinical development of vaccines and generates data that is used in preparation for future commercialization

Responsibilities

  • Managing various stability studies for novel vaccines during clinical development
  • Review and approval of various documents such as: protocols, reports and documentation for IND/cta filing
  • Provide support during scientific investigations
  • Provide support to several CMC projects

Requirements

  • PhD in chemistry, pharmacy or a related field
  • 2-3 years of working experience in a pharmaceutical setting
  • Flexibility and teamwork are two very important characteristics
  • GMP / QC experience is nice to have
  • Experience in working on stability studies is nice to have

Benefits

  • Employment: 1 year via Oxford Global Resources, with possible extension
  • Salary indication: €4200- €4600 bruto per month
  • Working hours: 40 hours/week
  • Region: Leiden

Vacancy number: 16505