Analytical Project Leader

Analytical Project Leader (m/f/d) – Basel-Stadt

Analytical Project Leader for our client in Basel.

In this role, you will join a highly motivated and experienced team of analytical scientists and take a leading role in the analytical development of synthetic molecule projects with a focus on peptides
, from early development through commercialization. This is an exciting opportunity to apply your expertise in a dynamic, fast-paced environment and make a meaningful contribution to the development of life-changing medicines.

• Lead analytical development activities for peptide-based drug substance and drug product projects from early development through commercialization
• Develop phase-appropriate control strategies for drug substances and drug products
• Coordinate and oversee analytical activities, including method development, optimization, validation, and generation of physicochemical data
• Ensure high-quality documentation, timely delivery of results, and adherence to quality and regulatory standards
• Collaborate closely with cross-functional stakeholders across technical development, quality, manufacturing, and external partners
• Coach and guide technicians and junior scientists; act as a central analytical point of contact within project teams
• Ensure all work is performed in compliance with cGMP, safety, and regulatory requirements
• Supervise internal laboratory work and/or analytical activities at external CROs/CDMOs
• Independently plan, execute, and document experiments and contribute to regulatory submissions (e.g., IND, NDA)

• Master's or Ph.D. in Chemistry, Pharmacy, or a related scientific discipline
• Minimum 3 years of industry experience in analytical development of peptide drug substances and/or drug products
• Strong expertise in peptide chemistry, including synthesis, purification, and characterization
• Hands-on experience with key analytical techniques such as HPLC, UPLC, and Mass Spectrometry (MS) for peptide analysis
• Proven experience with ICH-compliant analytical method development and validation
• Solid understanding of peptide degradation pathways, impurity profiling, and stability studies
• Experience defining specifications for peptide drug substances and/or drug products
• Strong quality mindset with excellent attention to detail
• Digital affinity to support data-driven and digital transformation initiatives; statistical data analysis skills are an advantage
• Open-minded, goal-oriented, and comfortable working in a fast-evolving environment
• Ability to view challenges as opportunities and collaborate respectfully under pressure
• Excellent command of English (written and spoken)

To apply, please submit your complete application documents through our online application form.

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