Analytical Development Chemist

hace 4 semanas

Barcelona, Barcelona, España Global Life Science Hub A tiempo completo
About the Role

We are seeking a highly skilled Analytical Development Chemist to join our team at Global Life Science Hub. As a key member of our analytical development team, you will play a pivotal role in the development of new analytical methods and supporting innovative pharmaceutical processes.

Key Responsibilities:
  • Method Development and Validation: Develop, qualify, and validate new analytical methods to support process development and other stages of drug development.
  • Sample Testing and Coordination: Coordinate sample testing and analytical activities, applying techniques such as reverse and normal phase (U)HPLC-UV, GC-FID, LC-MS, GC-MS, and more for drug substance analysis and control.
  • Data Review and Interpretation: Review and interpret external analytical data packages provided by customers.
  • Scientific Presentations and Team Collaboration: Present scientific data and participate in R&D group meetings, representing the Analytical Development team when necessary.
  • Analytical Tasks and Troubleshooting: Perform analytical tasks individually to support process development, regulatory submissions, and lot release. Troubleshoot analytical methods and resolve technical challenges during method development.
  • Compliance and Documentation: Ensure compliance with cGXP standards, regulatory requirements, and company procedures. Write and review technical reports, SOPs, and Tech Transfer documents, maintaining precise and accurate documentation.
Requirements:
  • Education: Degree in Chemistry, Analytical Chemistry, or a related discipline.
  • Communication Skills: Strong communication skills in English, both written and verbal (Spanish is a plus but not mandatory).
  • Experience: Minimum of 2-3 years of experience in an Analytical Development laboratory; experience in QC laboratories is also valuable.
  • Technical Expertise: Hands-on expertise in analytical techniques such as (U)HPLC-UV, GC-FID, LC-MS, GC-MS, and other drug substance characterization methods.
  • Collaboration and Methodology: Ability to work methodically and collaboratively within a team-oriented environment.

This role offers an exciting opportunity to work with a global leader in the CDMO industry, contributing to the development of new analytical methods and supporting innovative pharmaceutical processes.

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