Contractor Laboratory Specialist (f/m/d)
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Neuchâtel, Switzerland | 
Temporary Employment
Job title: Contractor Laboratory Specialist (f/m/d)
Industry: PharmaSkills: 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
