QC Associate Scientist/ Lab Professional (m/f/d)

Stein  ‐ Vor Ort
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Beschreibung

QC Associate Scientist/ Lab Professional (m/f/d)

Duration: 1 year

Location: Stein (CHF)

Department: Cell and Gene Bioanalytics

Tasks
  • Plan and perform Bio-Analytical testing such as Flow, ELISA, cell count, cell viability,re-sidual bead assessment, qPCR, Potency, in collaboration with experienced team members, if necessary.
  • Perform all testing and activities compliantly following appropriate SOPs and proce-dures.
  • Maintain controls, reagents and reference standards to support testing.
  • Work on shifts covering daytime / evening and one or both weekend days.
  • Review data generated by other team members.
  • Train others.
  • Contributes to the setup and optimization of infrastructure or specialized facilities e.g. cell culture or qPCR labs as an expert w/ adequate guidance.
  • Evaluate/qualify and maintain lab equipment.
  • Execute validation/transfers/optimization of test methods as per appropriate protocols.
  • Contribute to OOS/OOE and deviation investigations.
  • Interface with regulatory agencies during audits.
  • Support 5S and Lean projects.
  • Continually identify areas for improvements in project work.
  • Knowledge of LabWare LIMS and/or other QC data systems.
  • Maintain GMP/GLP quality systems.
  • Review of laboratory logbooks and laboratory cleaning.
  • Performing daily equipment startup and PQ


Requirements
  • Commercial degree as BTA or MTA or BSc degree
  • 2-5 years (for candidates with a Masters degree 0-2 years) industry working experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device industry.
  • Understanding of the concepts of GMP and GLP
  • Knowledge of bioassay test methods like Cell counts, Elisa, Flow cytometry.
  • Ability to communicate clearly with a variety of individuals in various aspects of operations.
  • Strong written and verbal communication skills are essential.
  • Ensure customer satisfaction and react to customer requests
  • Strong ability to work independently, compliantly and results driven.
  • Pays attention to detail
  • Able to proof work and identify non-standard format or wording, and errors within documents
  • Fluent in local site-language (English), German is desireable


Sthree Switzerland is acting as an Employment Business in relation to this vacancy.
Start
01/2021
Von
Real Staffing
Eingestellt
12.01.2021
Projekt-ID:
2027126
Vertragsart
Freiberuflich
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