Pharma

Analytical Chemistry Scientist – Small molecules, GMP

Switzerland / Contract

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Analytical Chemistry Scientist – Small molecules, GMP vacancy for a globally operating Basel based company in the Pharma sector.

We are looking for a highly motivated Senior Analyst/Analytical Expert to support Analytical Research & Development (ARD). ARD sits within the Global Technical R&D department of Development and plays an essential role in the characterization and analysis of Small Molecule Drug Substances and Drug Products from the time they leave the discovery laboratory until they are transferred to Commercial Production. The role will be part of the Small Molecules GMP Analytics Team with focus on small molecules and Radioligand Therapy.

Your tasks:

  •  Plan, execute and report results of scientific experiments for DS and/or DP applying state of the art analytical science and technologies (e.g., Release/stability/analytical method validation/ cleaning verification etc.) according to the agreed timelines. Ensure compliance to cGMP
  • Accountable for documentation and submission of raw data in an appropriate system (e.g. LIMS)
  • Responsible for good laboratory and documentation practices during execution of laboratory activities
  • Support in evaluation and interpretation of results including investigations on SST failure, OOx/Deviation as required
  • Review analytical documents (raw data review/approval, validation protocol, …..)
  • Provide scientific guidance to laboratory associates
  • Manage interactions and contribute to a high level of collaboration with internal and external stakeholders
  • Support audits and health authority inspections and ensure no critical findings within the assigned scope
  • Exhibit strong team spirit and promote knowledge exchange

Your experience/knowledge:

  •  Master degree in analytical chemistry or equivalent and a minimum of 5 year’s experience in the pharmaceutical industry
  • Strong expertise in analytical techniques, e.g. HPLC, Particle size, Dissolution testing, cleaning validation/verification, X-Ray, IR, etc..
  • GMP experience is a must
  • Experience with raw data review/approval
  • Experience in handling Deviations/OOx as a plus

Your soft skills:

  • Excellent comprehension skills with attention to detail
  • A high degree of self-organization and time management
  • Analytical and solution-orientated thinking
  • Communication skills including presentation and scientific/technical writing

 

Location: Basel, Switzerland
Work setting: On-site
Sector: Pharma
Start: 08/2025
Duration: 25 months
Workload: 100%
Ref.Nr.: BH 23178

Take the next step and send us your resume along with a daytime phone number where we can reach you.
Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens as well as current work-permit holders for Switzerland.
Ukrainian refugees are warmly welcomed, we will support you all the way.
We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application.

As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.

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