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Business Process Analyst Ii jobs at Teva in India
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Teva Quality Control Analyst II- Microbiology India, Goa
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To ensure receipt, registration and upkeep of samples in the laboratory. To complete review of microbiological testing reports related to (but not limited to) raw materials, finished products, stability. study...
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20.07.2025
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Teva Analytical R&D Analyst - TAPI India, Uttar Pradesh, Greater Noida
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Excellent communication and with hands on experience. Having working experience of analytical method development/ validation for HPLC/GC test methods, from different markets. Troubleshooting/OOS investigations during validations. Having a good knowledge...
20.07.2025
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Teva Regulatory Affairs Associate II India, Maharashtra, Navi Mumbai
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Develop US labeling documents to align with company goals and submission requirements for assigned ANDAs and/or 505(b)(2)s, if required, and ensure labeling meets all legal and regulatory requirements. This includes...
14.07.2025
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Teva Regulatory Affairs Associate II India, Maharashtra, Navi Mumbai
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Prepare, compile, review and submit high quality submissions for all required post-approval activities in accordance with EU legislation and in-house standards. Responsibility for MA compliance with both legislation and business...
08.07.2025
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Teva Quality Control Technician II - TAPI India, Uttar Pradesh
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Technical/functional knowledge in Costing, Inventory, Accounting and closing & reporting process area, with strong background of USGAAP. Managing all Costing & inventory related activities including accounting policies and memos, cost...
08.07.2025
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Teva Formulation Researcher II India, Maharashtra
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Bench scientist with good analytical acumen in the area of formulation research and development, process development, Regulatory and Intellectual property for global markets. Planning and conducting of experimentation in line...
08.07.2025
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Teva Quality Control Technician II - TAPI India, Uttar Pradesh
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Analysis of stability samples & working standard qualification activity as per defined procedure & monograph. Maintaining a set of procedure supporting to ATS department for (GMP & GLP) techniques implementation....
Description:Full job details
To ensure receipt, registration and upkeep of samples in the laboratory. To complete review of microbiological testing reports related to (but not limited to) raw materials, finished products, stability. study...
These jobs might be a good fit
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