Analytical Associate

Vor 2 Tagen

basel, basel city, Schweiz ITech Consult AG Vollzeit

Analytical Associate in Analytical Development for Synthetic Molecules – English / Analytical instruments

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 – apply now and help shape the future of healthcare

The Perfect Candidate The ideal candidate holds a vocational qualification in natural sciences or a Bachelor’s degree in Chemistry or Biochemistry, combined with several years of experience in the pharmaceutical industry. They bring proven expertise in instrumental analytics-such as HPLC, GC, KF, and MS-as well as solid experience in method development. Operating with strong quality awareness and exceptional attention to detail, they excel in precise scientific writing. A proactive, independent mindset along with fluent German and good English skills round out the profile.

Tasks &

Responsibilities:

Development and optimization of robust analytical methods (e.g., HPLC, GC, LCMS, 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