https://www.fradeo.com/de/kandidaten/deutsch-franzoesische-stellenangebote/senior-bioanalytical-scientist-department-head

Senior Bioanalytical Scientist – Department Head

  • Ulm
  • 29. Januar 2021
  • Ref. FRDJOB2021012915262530
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AXEPTA SA

Established in 2009, AXEPTA Talents is a Swiss recruitment agency specializing in five key sectors.

We are looking for a Senior Bioanalytical Scientist for one of our clients, based in Neu-Ulm, to join its LC/MS bioanalytical department and manage teams dedicated to small molecule bioanalysis using state-of-the-art LC/MS instrumentation.

Join a dynamic, international and fast-growing company and play a leading role in growing the organization and directing the team towards an industry-leading CRO in this field.

Responsibilities:

Thanks to your leadership and as the Department Leader, you will have to manage your teams working on bioanalytical activities.
 
  • Leading an LC/MS bioanalytical department for quantification of small molecules compounds consisting of operational managers, project managers and analysts.
  • Implementing large molecule bioanalytical work using LC/MS instrumentation.
  • Managing and coordinating work packages within the group in order to ensure optimal employment of resources and timely delivery of data and reports.
  • Peer review plans, data assessments and reports to ensure scientific excellence and adherence to SOPs and client’s requests.
  • Drive continuous improvement and excellence strategies for the department.
  • Assist and trouble shoot development and validation of bioanalytical methods for quantification of new molecular entities.
  • Act as a GLP test site manager according to German Chemicals Act.
  • Ensure adequate training of staff in order to further develop capabilities and ameliorate where gaps are identified.
  • Evaluate, develop, and implement new technologies, techniques, and skills in accordance with company strategy and follow literature especially in the area of sample preparation, mass spectrometry and laboratory automation.
  • Lead validation of computerized systems in accordance with applicable guidelines (OECD 17) and internal procedures and assume responsibilities as a process owner. 

Your profile : 

  • You have a scientific background in Life Sciences (e.g. pharmacy, chemistry, or food chemistry), ideally a PhD 
  • You also have previous relevant experience as study director/principal investigator in LC/MS bioanalysis in the pharmaceutical industry or at CROs in a GxP regulated environment (at least 10 years)
  • Hands-on experiences and troubleshooting skills in modern LC-MS/MS bioanalysis.
  • Professional experience in pharmacokinetic data evaluation including relevant software is required.
  • Sound understanding of R&D-related sciences/practices and knowledge of international regulatory principles and guidelines from health authorities (e.g., EMA, FDA, ICH).
  • With excellent leadership skills and sense of urgency, you are able to create a team spirit, commitment to objectives and clear accountability.
  • Fluent in English and German