Vacature - Jouw nieuwe functie

Scientist Viral Vector DSP

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Deel deze vacature

9 NOV '23: This Leiden-based organisation comprises a state-of-the-art facility and expert knowledge on the development, production, and commercialisation of Cell and Gene Therapies. They help academic and industrial developers enter the clinical stage by combining the required expertise in a brand-new development & GMP manufacturing facility. They enable the next generation of therapies by translating research programs into actionable health solutions for patients.




Leiden - Netherlands

40 uur per week

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Jouw consultant

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Zo maak jij het verschil

As Scientist Viral Vector DSP, you will be responsible for supporting the process development and/or manufacturing of Cell- and Gene Therapy products. You drive development (sub-) projects forward independently and contribute to maintaining the functionality, safety, and efficiency of laboratories and cleanrooms. Your tasks will include supporting CDMO activities (both GMP and non-GMP level), hands-on work in the development laboratory and cleanroom to support process development and analytics of Cell- and Gene Therapy products, co-design of process development (sub-)projects based on customer specifications, writing and maintaining SOPs and other manufacturing related documentation, maintenance and generation of cell lines, cell banks, virus seed stocks and plasmids. Lastly, you'll collaborate with Analytics and QC to support assay development and validation.

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Wat jij mee brengt

Being this strong Scientist, you will recognise yourself in the following:

  • PhD/MSc/BSc level education in a relevant field (biomedicine, biochemistry, biotechnology or similar);
  • At least 3 years of relevant work experience in the field of Viral Vector; 

  • Basic knowledge of GMP standards;

  • Strong verbal and written communication skills in English; 

  • Hands-on experience with the relevant platforms, processes, and systems used.

With the competencies:

  • Pro-active attitude; 
  • Thorough;
  • Self-organised;
  • Detail-oriented;
  • Problem-solving;
  • Co-operative;
  • Good record-keeping skills.

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Jouw voordelen

You will receive a competitive salary and an excellent pension plan. Not to mention the many opportunities and exciting dynamics of a scale-up environment and GMP training by their expert team. A standard full-time position at this organisation is 36 hours. In addition to your salary, you will receive:
  • A 13th-month payment and an 8% holiday allowance;
  • The unique opportunity to co-define the organisation and contribute to the organisation's establishment.
Your expertise is critical for their successful launch, meaning you will enjoy a lot of responsibility and impact regarding key decisions.


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