Stability Analyst
Teva Pharmaceuticals
The position forms part of the QC Laboratory Team. Main responsibilities include reviewing all PS data; compiling of stability protocols and reports; compiling of supporting documentation and logistical support for outgoing method transfers of stability studies; and to coordinate the necessary reservation and preparation of Production samples for Stability studies.
The ideal candidate must have a good eye for detail, be highly organised, accurate and methodical in his/her work. Good communication, documentation, and time management skills are necessary. Applicants must possess a diploma in Applied Science or a Degree in Science subjects (Chemistry, Biology or Medical Laboratory Science). Applicants having two Advanced Level qualifications in Science subjects (including Chemistry) will also be considered. Previous laboratory experience is considered an asset, although full training will be provided. The candidate must be computer literate and proficient in Microsoft Office applications.
Stability Coordinator
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
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