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Regulatory Affairs Associate Ii jobs at Teva in India
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20 jobs found
30.06.2024
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Teva Regulatory Affairs Associate II India, Goa
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Assess submission documentation in consideration and compliance with the regulatory requirements and to provide inputs to cross functional teams. Coordinate (on need basis) with external parties and cross functional teams...
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29.06.2024
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Teva Regulatory Affairs Associate II India, Maharashtra, Navi Mumbai
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Develop labeling documents to ensure alignment with the Reference Listing Drug. This includes QC, proofing, editing and formatting of documents, and coordinating the review and approval of final submission documents...
24.06.2024
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Teva Regulatory Affairs Associate India, Maharashtra, Navi Mumbai
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To organize and perform required regulatory tasks in order to maintain existing EU procedures in line with current regulations, guidelines and in-house standard. To obtain regulatory approvals for defined European...
23.06.2024
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Teva Regulatory Affairs Associate III India, Maharashtra, Navi Mumbai
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This position provides medical and scientific expertise for regulatory submissions and implies in-depth expertise within medical science, with primary goal of authoring clinical and non-clinical expert reports and summaries supporting...
24.06.2024
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Teva Sr Mgr Regulatory Affairs India, Maharashtra, Navi Mumbai
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Act as Project manager (PM) overseeing the support for new registrations using Teva’s proprietary products and achieving Marketing Authorisation (MA) for the Medis business. Focus on specific territories such as...
24.06.2024
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Teva Pharmacovigilance Associate II India, Karnataka, Bengaluru
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Participate in activities of literature review. Design and implement comprehensive literature search strategies on specific products. Knowledge of database: Embase, Medline, Pubmed, Ovid, etc. Assess the impact of regulatory changes...
06.07.2024
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Teva Operator II India, Uttar Pradesh
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Carrying out dispensing activities as per applicable procedure. Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards. Responsible for recording the observations...
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Assess submission documentation in consideration and compliance with the regulatory requirements and to provide inputs to cross functional teams. Coordinate (on need basis) with external parties and cross functional teams...
These jobs might be a good fit
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