Teva Pharmaceuticals jobs
To be qualified by education, experience and training to assume responsibility for proper conduct of the study.
Personally conduct and supervise the study.
Performing online documentation and preparing analytical data in accordance with
Teva standard procedures. Actively participate in investigation team and help…
The main tasks of the position includes as follows:
Preparation of data migration documents.
Perform source to target data mapping which requires detailed…
Will be working closely with third party for getting documents for compilation of new ANDAs filings and deficiencies responses.
Analysis, review and reporting of data, and disposal of stability samples.
Preparation and standardization of volumetric solutions, reagents and related…
Ensure equipment, machinery and lab areas as per EHS standards and safety.
Conducting EHS Training and awareness sessions as per statutory requirement.
Primary purpose and function of this position:
The ABAP MFG-QM Lead responsibilities include the following:
Create functional designs from technical perpective.
To Perform the Qualification /Requalification of Instruments/Equipment with proper documentation.
To check the calibration records and its proper documentation.
Prepare, compile, review and submit high quality submissions for all required post-approval activities in accordance with EU legislation and in-house standards.
Bachelor degree in technology, scientific or healthcare discipline.
Experience of 7 years working in total and 3 years GxP quality environment.
Essential Duties & Responsibilities and Percentage of Time.
Provide hands-on operational support (technology, out-of-the-box configurations, process and content…
Identify, create opportunities with
pharmaceutical companies (existing and new). The Account Manager is expected to maintain & expand
Teva api sales in the…
To monitor and perform Quality Check of all study activities from check-in, dosing, sample collection, processing, segregation, transfer and till checkout.
Experience in handling Quality Assurance issues related to the clinical department.
Experience in Planning,monitoring and handling study related documents in…
5+ years working in regulated (GLP, GCP or GMP) biotech or
pharmaceutical companies. Validation of software applications/modules and associated interfaces and…
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