Analytical Associate in Analytical Development for Synthetic Molecules

Flexsis

Basel

Vor Ort

CHF 90.000 - 120.000

Vollzeit

Vor 2 Tagen
Sei unter den ersten Bewerbenden
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Zusammenfassung

Roche in Basel is seeking an Analytical Associate in Analytical Development for Synthetic Molecules. The position is based in Basel, with start dates in late 2026, a 12-month contract, and 100% workload; home office is not available.

You will develop robust analytical methods (HPLC, GC, LC-MS, GC-MS, KF) to evaluate starting materials, intermediates and APIs, plan experiments, and collaborate with process development and QC teams to ensure smooth method transfers and regulatory documentation.

Qualifikationen

  • Completed vocational training in natural sciences or a Bachelor's degree in Chemistry/related field with at least 2-3 years pharma experience.
  • Solid experience with analytical instruments (HPLC, GC, KF, MS) and method development.
  • Strong scientific writing and ability to summarize results precisely.

Aufgaben

  • Develop and optimize analytical methods (HPLC, GC, LC-MS, GC-MS, KF) for quality assessment of starting materials, intermediates, and APIs.
  • Plan and carefully execute experiments including reaction monitoring and method development.
  • Collaborate with process development and cross-functional teams to coordinate analytics and sample management.
  • Work with QC to ensure smooth transfer of methods and documentation for validations and filings.
  • Create high-quality documentation and reports; apply innovative tools to improve workflows.

Kenntnisse

Analytical mindset
Scientific writing
Team collaboration
Proactive

Ausbildung

Bachelor's degree in Chemistry or related field

Tools

HPLC
GC
LC-MS
GC-MS
KF

Jobbeschreibung

Flexsis is a company of the Interiman Group, one of the leading providers of personnel services in Switzerland. Thanks to our solid expertise as well as the competencies within the Interiman Group, we offer tailored solutions in personnel consulting.

For our client Roche in Basel, we are looking for a reliable and motivated (m\/f\/d)

Analytical Associate in Analytical Development for Synthetic Molecules
  • Start date: 01.11.2026
  • latest Start Date: 01.12.2026
  • Planned duration: 12 months
  • Extension: likely
  • Workplace: Basel
  • Workload: 100%
  • Home Office: No
  • Development and optimization of robust analytical methods (e.g., HPLC, GC, LC-MS, GC-MS, KF) for the quality assessment of starting materials, intermediates, and active pharmaceutical ingredients (APIs).
  • Planning and meticulous execution of experiments, including reaction monitoring and method development.
  • Close collaboration with process development and cross-functional partners to coordinate analytical activities and sample management.
  • Close cooperation with the QC (Quality Control) unit to ensure a smooth transfer of the developed analytical methods.
  • Creation of high-quality documentation, including analytical procedures and reports that serve as the foundation for method validations and regulatory filings.
  • Application of an innovative mindset and digital tools for continuous improvement of analytical workflows in a dynamic environment.
  • Completed vocational training in natural sciences (Laboratory Technician) or a Bachelor's degree in Chemistry, Biochemistry, or a related field with at least 2-3 years of professional experience in the pharmaceutical industry.
  • Solid practical experience with analytical instruments (e.g., HPLC, GC, KF, MS) as well as strong expertise in method development.
  • Strong scientific writing skills and the ability to summarize and present results of complex experiments precisely
  • High quality awareness and uncompromising attention to detail, including work within a non-GMP development environment
  • Proactive, self-motivated work style and the ability to adapt quickly to new tools and processes in a dynamic team environment
  • Fluent English language skills (both spoken and written) and German is beneficial.
Nice to Haves:
  • Knowledge of GxP requirements and method validation is an advantage.
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