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Scientist, Peptide Drug Substances R&D

Job in 4416, Bubendorf, Kanton Basel-Landschaft, Switzerland
Listing for: Jobtailor
Full Time position
Listed on 2026-07-19
Job specializations:
  • Research/Development
    Research Scientist, Pharmaceutical Science/ Research, Drug Discovery
Salary/Wage Range or Industry Benchmark: 120000 - 150000 CHF Yearly CHF 120000.00 150000.00 YEAR
Job Description & How to Apply Below
Location: Bubendorf

Responsibilities

  • Responsible for planning, analyzing and interpreting experiments, and presenting the obtained results
  • Planning and timely execution of development activities and process optimizations in cooperation with other departments, taking quality, cost-effectiveness and safety into account
  • Performing process transfers (scale-up) and supporting production in the implementation of new processes, partly under cGMP guidelines
  • Focus on the LPPS/TAPS area (organic chemistry in solution, peptide couplings, protecting-group chemistry, extraction, precipitation, crystallization)
  • Writing reports and preparing presentations on the carried-out work for internal and external customers
  • Supporting production in resolving chemical challenges (troubleshooting)
  • Active participation in the continuous improvement of our equipment and workflows as well as maintenance of laboratory infrastructure
Requirements
  • PhD in Chemistry
  • Experience in preparative organic synthesis and an interest in process engineering
  • A structured, precise and independent working style that enables you to keep an overview at all times
  • Strong communication and organizational skills
  • Reliability, independence and a collaborative team spirit
  • Very good written and spoken German and English skills
  • Knowledge of peptide chemistry and common analytical techniques such as UHPLC and LC-MS is an advantage
Core Competencies

Demonstrates expertise in preparative organic synthesis, process engineering, and peptide chemistry, with strong capabilities in troubleshooting and process optimization under cGMP guidelines. Proficient in both written and spoken German and English, with a structured and independent working style that supports effective communication and collaboration.

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