Scientist - Analytical Development

hace 2 semanas

Pamplona, Navarra, España Pivot Park A tiempo completo
Associate Scientist - Analytical Development

The analytical laboratory plays a key role in the development and validation of analytical methods to characterize active pharmaceutical ingredients (API) in different stages of pharmaceutical development. As an Associate Scientist in the Analytical Sciences department, you will implement, develop and validate chromatographic methods.

Your Key Responsibilities:
  • You implement, develop, and validate chromatographic methods for analysis of starting materials, intermediates, and drug substances.
  • You apply these methods in development projects, e.g., to support process development, stability studies and for release analyses.
  • You will write analytical methods, prepare protocols and reports containing analytical results from, e.g., method development, stability and validation reports.
  • You will collaborate with other colleagues from R&D, manufacturing and quality assurance as to advance projects through development.
  • You keep yourself up to date with the latest technical and CMC developments as well as insights into your area of expertise.
Your Profile:
  • You have a bachelor's or master's degree in Analytical Chemistry.
  • You have at least 1-3 years of experience with LC and (HS)GC.
  • You have experience in method development and/or method validation.
  • You have a good understanding of chemical structures and physical properties of materials that you can apply in the development of analytical methods.
  • You excel in translating characterization challenges into practical analytical solutions.
  • You are flexible, a problem solver and a team player with an analytical mindset.
  • You have good communication skills and are fluent in English (written as well as spoken).
  • You feel comfortable in a dynamic and changing environment.
  • You like to learn and develop yourself.
  • You are pro-active and you have a hands-on mentality.
  • Ideally, you have experience with cGMP and knowledge of ICH guidelines.
What We Offer:
  • A competitive salary with a tailor-made benefits package, including: pension plan, bonus systems and the possibility of purchasing additional leave.
  • Flexible working hours and 30 days of paid holiday per year.
  • A dynamic, international work environment with career growth opportunities.
  • Access to Ardena Academy, our internal learning platform for professional development.
  • A chance to contribute to groundbreaking drug development projects that make a real impact.

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