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Manager Analytical Development

Job in 4040, Basel, Kanton Basel-Landschaft, Switzerland
Listing for: K-Recruiting Life Sciences
Full Time position
Listed on 2026-09-01
Job specializations:
  • Pharmaceutical
    Pharmaceutical Science/ Research, Regulatory Compliance Specialist
  • Research/Development
    Pharmaceutical Science/ Research, Research Scientist, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 120000 - 180000 CHF Yearly CHF 120000.00 180000.00 YEAR
Job Description & How to Apply Below

(Senior) Scientist Analytical Development (M/W/D)

This role is a (senior) scientific position within an analytical development function focused on synthetic (small molecule) pharmaceuticals. It sits in a global technical development environment, supporting products from early development through commercialization. The position involves contributing to advanced analytical strategies, cross-functional collaboration, and regulatory submissions.

Tasks:
  • Lead / contribute to analytical development activities across the full product lifecycle (early stage to market).
  • Define and implement phase-appropriate control strategies for drug substances and drug products, including impurities.
  • Coordinate analytical testing, including method development, optimization, validation, and data generation (e.g., stability, physico-chemical characterization).
  • Collaborate cross-functionally with process development, manufacturing, quality, regulatory, and external partners.
  • Ensure high-quality documentation for regulatory submissions.
  • (Act as a technical lead, mentoring junior scientists and technicians and serving as a key project contact.)
  • Support innovation initiatives such as new technologies, digitalization, and process harmonization.
Qualifications:
  • MSc or PhD in chemistry, pharmacy, or a related scientific field with several years of industry experience.
  • Strong background in analytical development for small molecules (ideally peptides), including regulatory filing support (e.g., IND/NDA) and impurity control strategies.
  • Expertise in liquid chromatography (HPLC/UHPLC) with multiple detection techniques (e.g., UV, MS, fluorescence, CAD).
  • Solid understanding of quality control and GMP across development phases.
  • Familiarity with statistical analysis and digital tools is advantageous.
  • Strong communication and collaboration skills; able to work in cross-functional teams.
  • Fluent in English; additional languages are a plus.
  • Experience with complex modalities (e.g., peptides or oligonucleotides) is beneficial.
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