Applies GMP/GLP in all areas of responsibility, as appropriate
Applies the highest quality standard in all areas of responsibility
Demonstrates and promotes the company vision
Demonstrates strong client service skills, teamwork, and collaboration
Proactively plans and multitasks to maximize productivity
Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration
Regular attendance and punctuality
Supporting lab work associated with development and scale-up projects within the large molecule group
Demonstrate a working experience with aseptic technique
Perform duties in a protocol-driven work, such as passaging and sampling cell cultures, and running Ambr bioreactors,
Use of analytical instruments to monitor bioreactors
Assist with general lab upkeep and organization efforts, which includes decontamination and disposal of large scale cell culture wastes
Responsible for organizing records, capturing results into data sheets and contributing to technical reports in a team environment as well as contributing individually to meet project timeline and objectives.
Analyze and present data in professional format;
Demonstrate clear and professional verbal and written communication;
Conduct, analysis and reporting of data in accordance with requirements set forth by the department;
Ensure maintenance of detailed documentation of assay development and qualification;
Record experimental data and accurate and highly organized laboratory notebooks
Follow appropriate SOPs and all internal documentation requirements.
Bachelors or Master’s degree in biopharmaceutical, biotechnology or pharmaceutical required
Broad knowledge in upstream process development and hands-on experience is desired.
Experience with cGMP practices
Occasional weekend work might be required.
All your information will be kept confidential according to EEO guidelines.
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