Analytical Associate in Analytical Development for Synthetic Molecules (m/w/d)

Randstad Switzerland; Basel; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Zusammenfassung

Randstad Switzerland is seeking an Analytical Associate for our pharmaceutical client in Basel. The role sits in Analytical Development for Synthetic Molecules, employing HPLC, GC/LC-MS, and KF to develop robust analytical methods and support material release for clinical trials and commercial supply.

You will plan experiments, validate methods, and collaborate with process development and QC to ensure smooth transfers and regulatory documentation.

Qualifikationen

• Completed Bachelor's degree or equivalent in a natural science with practical experience in pharma.
• Strong ability to plan and document experiments and summarize results clearly.
• Experience with analytical instrumentation and method development is required.

Aufgaben

• Develop and optimize analytical methods (HPLC, GC, LC-MS, KF) for APIs and intermediates.
• Plan experiments and monitor reactions with accurate sample handling.
• Coordinate with process development and cross-functional teams to manage analytical activities.
• Collaborate with QC to ensure smooth transfer of methods.
• Create high-quality procedures and reports for method validation and regulatory filings.
• Apply innovative thinking and digital tools to improve analytical workflows.

Kenntnisse

Analytical thinking

Scientific writing

Team collaboration

Ausbildung

Bachelor's degree in Chemistry or related field

Tools

HPLC

GC

LC-MS

KF

Jobbeschreibung

For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a dedicated Analytical Associate.

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.

General Information:

• Duration: 1 year
• Extension: likely
• Contract type: Temporary contract via Randstad (employment)
• Work Location: Basel
• Home Office: not possible
• Working Hours: Standard

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 environment.

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)

Nice to Have:

• Knowledge of GxP requirements and method validation

Take a leading role in the development of innovative analytical techniques while contributing to the success of clinical and commercial therapies