Stability Scientist


DPS Group Global is currently looking for a Stability Scientist for the Analytical Development Department.

Chemist Industrial
Years of Experience Req.:
>3 years
Date Posted:
Days Remaining:
Employment Type:
Education Level Req.:
MSc or PhD degree


DPS is a leading Project Management and Engineering Company serving industry around the world for 40 years. Our reputation is based on forming successful partnerships with our clients, providing them with innovative designs and cost effective solutions in the context of sound judgment, strong management and technical excellence.
We provide Full Service Engineering for our clients including Project and Programme Management, Procurement, Design, Construction Management, Health and Safety Management, Commissioning, Qualification and Start-up on numerous projects across a range of market sectors. Our Main market sectors are; Pharmaceutical and Biotechnology, Medical Technologies, Oil & Gas, Advanced Technology, Science & Education, Food & Beverage, and Energy.



Analytical development quality team is part of the Analytical Development Department and focuses on the design, execution and evaluation of stability profiles and qualification of Reference Materials for novel vaccines. The group supports the clinical development stages of the vaccines platforms and generates data that is used in preparation for future commercializ72713.2392216ation.


Job description

  • The Scientist will be a key player in the management of the various stability studies of the novel vaccines during the clinical development.
  • Additionally, he/she will work in a multidisciplinary environment and have a focus on review and approval of various scientific protocol, reports, documentation for IND/CTA filing, provide support during scientific investigations. 
  • Since the scientist is providing support to various CMC projects that are carried out in teams comprising members from different departments, teamwork and flexibility are two very important characteristics that are required attributes.
  • We offer a challenging position which allows you to work in a dynamic and international environment, ensuring diversity in your work and creating plenty of opportunities for personal development.



  • MS or Ph.D. Degree in Biochemistry, Pharmacy, or equivalent life sciences degree
  • A minimum of 2-3 years pharmaceutical industry experience working under GMP standards.  
  • Experience with stability study management
  • Experience with analytical methods qualification and validation
  • Knowledge of statistical analyses and data trending
  • Knowledge of GMP quality systems, quality management



  • The candidate fit for the job is independent, flexible, motivated and enjoys working in a team. Excellent organiz72713.2392216ational and communication skills, and a strong scientific mindset are key for this position


Available and interested?

If you’re interested in this role and if you want to be part of growing organisation within engineering projects in the pharma industry or if you would like to discuss this vacancy further and to discuss your career options in confidence, please telephone Ralf Huisman on +31 6 11408791 or send your CV to

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