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•Process Engineer at the MS&T (Manufacturing, Science & Technology) department at “TEVA Kfar-Saba” site.
•Specialist in sterile products including manufacturing processes, critical parameters, technologies and pharmaceutical best practices.
•Lead new sterile products activities including transfer from R&D to operations, scale up, Process Validations and implementation of new technologies.
•Conduct root cause analysis, risk assessments and problem solving.
•Authoring manufacturing batch records, validation and characterization protocols and reports.
•Close interface with different units such as QA, production, QC laboratories, supply chain and more.
Focal point for different R&D units around the globe for development activities taking place at the site, such as submission batches, process design activities etc.
•Chemical\Biotechnology\Materials\Biomedical Engineer or similar scientific field
•Pharmaceutical experience - Significant Advantage
•Project Management and leadership skills – Must
•High ability to work independently, high interpersonal skills
•Highly motivated, willingness for hard work including extra hours
•Strong English abilities (the role involves comprehensive communications with colleagues abroad)
Sarit Ben Moshe
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