Analytical Associate in Analytical Development for Synthetic Molecules
For our client Roche in Basel, we are looking for a motivated and reliable (m/f/d).
Perfect Candidate: holds a solid vocational qualification or a bachelor’s degree in Analytical Chemistry, Biochemistry, Biotechnology, or a related field, with 1–3 years of hands‑on experience in analytical method development within the pharmaceutical industry. Proficient in analytical techniques such as HPLC, GC, and KF, apply GxP principles confidently, and possess strong scientific writing and documentation skills. With an innovative and quality‑driven mindset, they demonstrate adaptability, digital fluency, reliability, and a proactive, collaborative approach in a dynamic environment.
General Information:
* Planned Duration of Employment: 12 months
* Extension (for temporary contracts): extension need to be discussed
Tasks & Responsibilities:
* Development, improvement and validation of analytical methods for the quality assessment of starting materials, intermediates, reaction monitoring, active substances and galenical forms.
* Thorough and efficient planning, execution and documentation of experiments in collaboration with relevant team members, analytical project lead and supervisor, following current GxP guidelines and relevant SOPs.
* Work on end‑to‑end processes in close collaboration with other associates, scientists, and partners from other departments to ensure efficient analytics and continuous improvement.
* Coordination of analytical activities including sample management for the development of synthetic products.
* Authoring of documents, e.g., analytical procedures, validation reports.
* Routinely apply GxP requirements where necessary, and understand how to exert them in different clinical phases.
Must Haves:
* Solid vocational qualification with at least 1–3 years’ experience in the pharmaceutical industry focused on analytical methods development (chromatography) or a bachelor’s degree (Analytical Chemistry, Biochemistry, Biotechnology). No further academic qualifications required.
* Hands‑on experience in analytical instrumentation and techniques (e.g., HPLC, GC, KF).
* Routinely apply GxP requirements where necessary, and understand how to exert them in different clinical phases.
* Excellent command of English. Good command of German would be a plus.
* Strong interest / background in analytical methods development.
* Good scientific writing style and documentation practice for regulatory filings.
Are you interested? Then we should definitely get to know each other! Simply click on "Apply now" and we look forward to receiving your complete application documents.
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