Analytical Associate / Analytical Associate

Tasks & Responsibilities

As a key member of our team, you will be responsible for:

• 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.
• Collaborating closely with process development and cross-functional partners to coordinate analytical activities and sample management.
• Working in conjunction with the QC (Quality Control) unit to ensure a smooth transfer of developed analytical methods.
• Creating high-quality documentation, including analytical procedures and reports that serve as the foundation for method validations and regulatory filings.
• Applying 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 from complex experiments clearly and effectively.
• High quality awareness and an uncompromising attention to detail, including experience within a non-GMP development environment.
• Proactive and self-motivated work style with the ability to adapt quickly to new tools and processes in a dynamic team environment.
• Fluent English language skills (both spoken and written); proficiency in German is a plus.

Apply online using the form below. Please note that only applications matching the job profile will be considered.