Analytical Development Scientist – (cGMP) – 6966 URA

 

Our client is a leading Swiss multinational healthcare company headquartered in Basel, Switzerland. Operating in Pharmaceuticals and Diagnostics, it is one of the world’s largest biotech companies and a global leader in in-vitro diagnostics and cancer treatments. Our client is known for its strong focus on innovation, particularly in personalized healthcare, and has played a major role in developing treatments for oncology, immunology, infectious diseases, and neuroscience.

 

The perfect candidate for this role has a Master’s degree (or higher) in Organic Chemistry, Analytical Chemistry, or Pharmacy, at least 3 years of professional experience in Quality Control, and very good GMP knowledge. This role is a 12 months contract to be based in Basel.

Main Responsibilities

  •  Work in a modern quality control organization in compliance with cGMP regulations.
  • Cooperation with internal and/or external partners of Analytical Development
  • Active participation in shaping the working methods of the analytical group
  • Comprehensive analytical support for supply plants for API and drug product for clinical use
  • Critical evaluation of own work results
  • Support the analytical group by fulfilling cross-laboratory tasks and project tasks (e.g.reference standard management, CSV business process owner of analytical applications)
  • Implementing and fully complying with relevant Roche policies, procedures, and standards in the areas of safety, health, and environmental protection
  • Ensuring that laboratory employees are informed of all relevant SHE requirements and their implementation
  • Ensuring an appropriate GMP standard in the laboratory
  • Scientific and regulatory documentation of the work done

 Qualifications and Experience:

 

·      Relevant Swiss working/residency permit or Swiss/EU-Citizenship required

·      Bachelor’s or Master’s degree in Natural Sciences OR a Laboratory Technician with 10+ years of high-level GMP experience

·      3–5 years of professional industry experience with a core focus on Analytical Chemistry

·       Practical experience working under cGMP regulations is required

·      Proficiency in laboratory-specific software (e.g., Waters Empower, Metrohm Tiamo, or Labware LIMS)

·      English (Fluent/Mandatory). German language skills are considered a significant advantage

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