Analytical Associate in Analytical Development for Synthetic Molecules

Interiman group - Flexsis; Basel; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Zusammenfassung

Roche in Basel invites applications for an Analytical Associate in Analytical Development for Synthetic Molecules. Start date 01.11.2026 or 01.12.2026, 12-month assignment, 100% workload, Basel.

You will develop and optimize analytical methods (HPLC, GC, LC-MS, KF) for quality assessment of starting materials, intermediates, and APIs, and collaborate across process development and QC to ensure smooth method transfer and robust documentation.

Qualifikationen

• Completed vocational training in natural sciences or a Bachelor's degree in Chemistry/Biochemistry with relevant experience.
• Experience with analytical instruments (HPLC, GC, KF, MS) and method development.
• Strong scientific writing and precise data presentation.

Aufgaben

• Develop and optimize analytical methods (HPLC, GC, LC-MS, KF) for APIs and intermediates.
• Plan and execute experiments with careful sample management and reaction monitoring.
• Collaborate with process development and QC to transfer methods and ensure documentation quality.
• Create high-quality documentation and reports supporting method validations and filings.
• Apply innovative thinking to improve analytical workflows in a dynamic team environment.

Kenntnisse

Analytical method development

Scientific writing

Documentation

GxP knowledge (nice to have)

Ausbildung

Bachelor's degree in Chemistry or Biochemistry

Laboratory Technician training

Tools

HPLC

GC

KF

LC-MS

Jobbeschreibung

Functieomschrijving

Description of the company

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

Role & Responsibilities

• 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.

Candidate Profile

• 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.