Scientist Process Development

  • Leiden
  • 4500.00 - 6000.00
  • 32-40 hours
  • Master degree

Client

Our client is a leading project management and engineering company for industry worldwide.

Client

Our client is a leading project management and engineering company for industry worldwide. Their reputation is based on forming successful partnerships with their clients, providing them with innovative designs and cost-effective solutions in the context of sound judgement, strong management and technical excellence.
They provide Full Service Engineering for their clients, including project and programme management, procurement, design, construction management, health and safety management, commissioning, qualification and start-up for numerous projects in various market sectors.

Requirements

  • Preferably a Ph.D. degree or MSc degree in biopharmaceutical sciences, biotechnology or related fields
  • A proven experience in late-stage pharmaceutical development and GMP drug product manufacturing, including technology transfers of vaccines.
  • In-depth knowledge of regulatory submission writing, technology transfer and process improvements
  • Experience with life cycle process validation
  • Good communication and interpersonal skills with stakeholders
  • Excellent written and oral communication skills in English

What do you get?

  • Pension entitlement as from day one
  • Collective WGA / WIA insurance
  • NBBU / ABU collective labor agreement
  • 25 holidays days
  • 8,33% holiday allowance
  • 100% payment in case of illness after one waiting day
  • Travel allowance

Duties

  • Develop fill/finish processes and technology transfer of innovative vaccines
  • Understand and provide input to define the technical content of the registration dossier, by guaranteeing availability of source documentation and data of vaccines
  • Setup, report and timely execute process development, characterization and validation activities, which can be done in-house or externally
  • Lead and participate in specialized committees, to ensure continuous improvement on departmental and project level
  • Establish and maintain a trustful and professional relationship with the stakeholders from departments within the company as well as with external partners

TAGCLOUD

vaccines
#drug
#pharma
#registration
#validation
#biopharmaceutical
#biotech
#GMP
Bas Lokhorst

Interested

Send your resume to bas@tailorminds.com referring to job id (1023)

More information?

Please contact Bas Lokhorst working at our office in Zoetermeer, phone number +31 6 82 43 66 08

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