Position: Associate

Job type: Full-time

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Job content

Ihr Aufgabengebiet
  • Disciplinary and organizational management of the lab team (approx. 10 heads)
  • Work & test planning based on priorities & deadlines
  • Budget planning as well as target/actual control
  • Further development and maintenance of the GMP compliant Quality Management System
  • Maintenance of GMP compliance in the laboratory
  • Ensuring instrument suitability (qualification/calibration)
  • Revision and release of SOPs
  • Review and approval of GMP relevant documents (e.g. validation reports)
  • Ongoing implementation of new regulatory requirements
  • Management of external and internal audits/inspections as main contact person in the laboratory environment
  • Participation in (inter-)national appointments (e.g. customer visits or conferences)
Ihr Hintergrund
  • Successfully completed studies in the natural sciences
  • Relevant professional experience as well as experience in laboratory management
  • Expert knowledge in the field of bioprocess engineering and/or process validation
  • Experience with audits/inspections
  • Fluency in English
Vertragsart: Festanstellung

Branche: Biotechnology

Fachbereich: Quality

Ort: Kassel Deutschland

Starttermin: Sofort

Dauer: Unbefristet

Remote: nein

Auslastung (FTE): 1
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Deadline: 08-12-2024

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