Jan Smith Email & Phone Number | Sound scientific skills combined with intimate knowledge, and strong communicative competence enable translation of customer needs into successful practical analytical solutions in-company or external. Currently involved as research analyst in the analytical method transfer of complex generic technology transfer. Moreover, as part of the team support 24/5 the first non-commercial production batches for registration purposes and the first non-commercial stability program. As team member responsible for all occuring tasks from performing method assesments, writing method documents and transfer, verification and validation protocols, execution of the same protocols, and summarizing the studies inreports. Draft versions of protocols and reports are discussed with QA department,

Jan Smith

Sound scientific skills combined with intimate knowledge, and strong communicative competence enable...
Woerden, Utrecht, Netherlands

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Jan Smith’s Email jan.smith@teva.nl

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Jan Smith’s Location Woerden, Utrecht, Netherlands

Jan Smith’s Current Industry Teva Nederland

Jan Smith’s Prior Industry Teva Pharmachemie | Crystallics | Synthon

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Analyst II - Method Implementation - Quality Analytical Laboratories at Teva Nederland

2020-07-01 00:00:00 - Present

Research Analyst - Method Implementation - Quality Innovative Laboratory

2019-03-01 00:00:00 - 2019-12-01 00:00:00

project leader solid state

2014-06-01 00:00:00 - 2014-11-01 00:00:00

Specialist Physchem Characterisation Platform Analytical Research group

2010-01-01 00:00:00 - 2014-05-01 00:00:00

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Jan Smith is a Sound scientific skills combined with intimate knowledge, and strong communicative competence enable translation of customer needs into successful practical analytical solutions in-company or external. Currently involved as research analyst in the analytical method transfer of complex generic technology transfer. Moreover, as part of the team support 24/5 the first non-commercial production batches for registration purposes and the first non-commercial stability program. As team member responsible for all occuring tasks from performing method assesments, writing method documents and transfer, verification and validation protocols, execution of the same protocols, and summarizing the studies inreports. Draft versions of protocols and reports are discussed with QA department,