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for the selection, cell line development, scale-up, and transfer of biologics (eg monoclonal antibodies and recombinant proteins). You will creatively utilize advances in machine learning and predictive analytics
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development plans, participate in cross-disciplinary forums & learning opportunities. Demonstrate and model adherence to all Pfizer behaviors & values, embrace and comply with Global Chemistry Manufacturing and
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communication skills. Systems and Document compilation skills, including: Must have excellent computer skills and be proficient with Microsoft Word and similar applications. Prepare submission ready documents
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development plans, participate in cross-disciplinary forums & learning opportunities. Demonstrate and model adherence to all Pfizer behaviors & values, embrace and comply with Global Chemistry Manufacturing and
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, HR policies) and individual development plans, participate in cross-disciplinary forums & learning opportunities. Demonstrate and model adherence to all Pfizer behaviors & values, embrace and comply
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. Nice-to-Have ASQ/CQA Certified Quality Auditor or ASQ/CQA-Certified Quality Engineer Strong computer proficiency skills in MS Office, Word, Excel, Access, Project, Learning Management Systems, document
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Faculté de biologie et de médecine de Lausanne | Lausanne, Canton de Vaud | Switzerland | about 1 month ago
of primary immune cells including lentivirus, retrovirus, Sleeping Beauty and CRISPR – Cas9. Expertise in T cell receptor (TCR) and chimeric antigen receptor (CAR) design and co-engineering strategies
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computer, equipment, utility, cleaning or process Verification/Qualification/Validation within the pharmaceutical industry. Thorough knowledge of cGMP (current Good Manufacturing Practices) and industry
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. • Relevant professional experience with Big Data systems, pipelines and data processing • Preferred experience in Applied Econometrics, Statistics, Data Mining, Machine Learning, Analytics, Mathematics
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for the establishment and execution of the validation strategy for a given sector of validation (i.e. equipment, computer system validation, etc.) to ensure that the validation documentation is compliant with plant and