MSAT Development Specialist

☞ DPS Group Global

Visualizza: 165

Giorno di aggiornamento: 16-11-2025

Località: Geel Antwerp

Categoria: Consulenza / Servizio Clienti Scienza

Industria: Pharmaceutical Manufacturing

Posizione: Mid-Senior level

Tipo di lavoro: Full-time

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Contenuto del lavoro

Responsibilities and Objectives:

Our client is a biotechnological production site for therapeutic proteins. The production of these proteins takes place via cell cultures in bioreactors, followed by a purification process and quality control. Product quality is verified through a wide range of analytical methods.

In this position the focus is on the analytical methods used during quality control, during product characterization and/or in additional research.

From a thorough scientific and technical specialization, you ensure the development and implementation of high-performance analytical technologies in support of existing and new production processes by:

  • Support designing/developing/improving/validating existing analytical methods
  • Independently set up experiments and develop and carry out studies
  • Provide documentation through generation of scientific/technical study protocols and reports
  • Maintain, adjust and communicate documentation and knowledge.
  • Data trending and monitoring of ongoing methods, experiments and analyzes to ensure reliability, as well as have an accurate understanding of the effectiveness and efficiency of the methods

Profile:

  • You obtained (preferably) a PhD in Life Sciences or are equivalent through experience
  • You have a very good knowledge of English and Dutch, both written and oral
  • Specific experience with analysis techniques eg HPLC/UPLC, MS, ion-exchange, binding, capillary electrophoresis, immunological assays, ect.
  • You have excellent problem-solving skills and can handle multiple (practical) tasks at the same time
  • You have good technical writing skills and are able to prepare protocols and reports
  • You are accurate, result-oriented and able to critically analyze data and draw scientifically sound conclusions and formulate them correctly
  • You have an excellent knowledge of cGMP and can convert legal requirements regarding analytical methods into effective action plans
  • You are a team player and have good communication skills
  • You are flexible, stress resistant, open to change & innovation and are used to working with deadlines
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Scadenza: 31-12-2025

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