Contractor Laboratory Specialist (f/m/d)

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Neuchâtel, Switzerland | 
Temporary Employment
Job title: Contractor Laboratory Specialist (f/m/d)
Industry: Pharma
Skills: Upstream/Downstream,ELISA
Start of project: 03.06.2024
Duration of the project : 6 months
Project volume: 1008 Hour(s) 
Location: Neuchâtel, Switzerland

RESPONSIBILITIES:

 

  • Conduct laboratory studies across various scales, including flask and bioreactors of different sizes, while utilizing diverse measurement instruments for monitoring cell culture processes.
  • Perform small-scale purification processes, such as chromatography and ultrafiltration, and execute column packing operations using resins of varying diameters.
  • Gather, condense, and analyze data for the preparation of reports and presentations.
  • Provide support for investigations concerning laboratory deviations.
  • Manage documentation linked to laboratory activities.
  • Explore and integrate innovations in the field to enhance performance.
  • Develop and refine process parameters.
  • Assist in experimental study design and protocol drafting.
  • Execute protocols as per supervisor or project lead directives, encompassing development, investigation, and process qualification.
  • Generate study reports and presentations of results.
  • Oversee maintenance and resolution of operational issues with laboratory equipment under responsibility.
  • Handle inventory and stock management of consumables essential for laboratory tasks.
  • Contribute to logistical activities within the laboratory.
  • Undertake additional assigned duties as needed.

REQUIREMENTS:

  • Possess a Master's degree in biochemistry, biology, biotechnology, or equivalent, coupled with 2 years of experience in the pharmaceutical sector, preferably in process development.
  • Demonstrate practical or theoretical expertise in recombinant protein purification (chromatography, ultrafiltration) and cell culture using CHO cells.
  • Proficiency in utilizing Windows-based software including Excel, Word, and Powerpoint.
  • Familiarity with analytical tools for recombinant proteins such as ELISA, SDS, and HPLC is desired.
  • Knowledge of statistics is advantageous.
  • Previous exposure to cGMP environments or familiarity with GMP principles is beneficial.
  • Exhibit willingness and comfort in a laboratory environment.
  • Possess strong communication skills and a collaborative mindset, including the ability to listen, exercise diplomacy, and take initiative.
  • Capable of effective verbal and written communication across various organizational levels.
  • Demonstrate strong organizational skills, attention to detail, and follow-up capabilities.

Fluent in French with a good command of English (minimum level B2).

Reference number: 14237
Industry: Pharma
Project start: 03.06.2024
Duration: 6 months
Employment type: Temporary Employment
Contact
Pawel Jasionek
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