Analytical Associate in Analytical Development for Synthetic Molecules

Flexsis AG, Filiale Basel LS; Basel; Vor Ort; CHF 90.000 - 130.000; Vollzeit

Zusammenfassung

Roche in Basel seeks an Analytical Associate in Analytical Development for Synthetic Molecules. The role focuses on developing and optimizing analytical methods (HPLC, GC, LC-MS, KF) for starting materials, intermediates, and APIs.

You will plan experiments, monitor reactions, and collaborate with QC and process development to ensure robust transfer of methods. The position is 100% workload, office-based in Basel, for 12 months with extension likely.

Qualifikationen

• Proven experience with analytical instrument platforms (HPLC, GC, MS).
• Experience in method development and optimization for pharmaceuticals.
• Strong scientific writing and data presentation skills.

Aufgaben

• Develop and optimize robust analytical methods for in-process materials and APIs (HPLC, GC, LC-MS, KF).
• Plan and execute experiments with precise documentation and traceability.
• Coordinate analytical activities with process development and QC to ensure smooth transfers.
• Create high-quality procedures and reports supporting method validation and regulatory filings.
• Apply innovative digital tools to improve analytical workflows in a dynamic setting.

Kenntnisse

HPLC

GC

LC-MS

Method development

English proficiency

German (beneficial)

Ausbildung

Bachelor's degree in Chemistry, Biochemistry, or related field

Laboratory Technician training

Tools

MS data analysis software

Jobbeschreibung

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.