Analytical Associate in Analytical Development for Synthetic Molecules

Elan Personal AG; Basel; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Zusammenfassung

F. Hoffmann-La Roche AG in Basel seeks an Analytical Associate in Analytical Development for Synthetic Molecules to drive method development for APIs and intermediates. You will work across HPLC, GC, LC-MS with cross-functional teams to ensure robust analytics for clinical and commercial supply.

The role emphasizes rigorous documentation, regulatory support, and collaboration in a dynamic PTD environment. Fluent English is required; German is a plus.

Qualifikationen

• Completed vocational training in natural sciences or a Bachelor's in chemistry/biochemistry with pharma experience.
• Strong hands-on experience with analytical instruments and method development.
• Clear scientific writing; ability to summarize complex data precisely.
• High quality awareness in non-GMP development environments.
• Proactive, self-motivated, adaptable to new tools in a team.
• Fluent English; German is a plus.

Aufgaben

• Develop and optimize robust analytical methods (HPLC, GC, LC-MS) for APIs and intermediates.
• Plan and execute experiments, monitor reactions and develop methods.
• Collaborate with process development and cross-functional partners for analytics.
• Coordinate transfer of methods to QC and ensure proper documentation.
• Create high-quality procedures and regulatory filings support documents.
• Apply innovative mindset and digital tools to improve workflows.

Kenntnisse

HPLC

GC

MS

KF

Method development

Documentation

Ausbildung

Laboratory Technician training

Bachelor's in Chemistry/Biochemistry

Jobbeschreibung

Roche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for a

Analytical Associate in Analytical Development for Synthetic Molecules

Background:

Pharma Technical Development (PTD) is a global team of over 2,000 experts dedicated to developing innovative medicines to meet patient needs

Within PTD, Synthetic Molecules Technical Development (PTDC) specializes in active pharmaceutical ingredients (APIs), drug products, and analytical sciences. PTDC plays a vital role in advancing the synthetic molecules pipeline, supporting research, early development, and clinical trials through technical innovation and collaboration.

This position is located within the Analytical Development for Synthetic Molecules department, where cutting-edge techniques such as High-Performance Liquid Chromatography (HPLC), Gas/Ion Chromatography (GC/IC), and Mass Spectrometry (MS) are used to develop efficient and robust analytical methods. The goal is to ensure product release for clinical trials and subsequent commercial supply through a rigorous control strategy.

Take a leading role in the development of innovative analytical techniques while contributing to the success of clinical and commercial therapies — and help shape the future of healthcare!

Tasks & 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 environmen

Must Haves:

• 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 Have:

• Knowledge of GxP requirements and method validation is an advantage.

What you will be offered:

• An opportunity to work in one of the world's most important pharmaceutical companies
• Modern campus with plenty of green spaces and meeting areas
• Central location in Basel
• Varied job profile
Further training opportunities through temptraining
• Working in a dynamic and motivated team