Manager Analytical Development
Job in
4040, Basel, Kanton Basel-Landschaft, Switzerland
Listed on 2026-09-01
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
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.
- 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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