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Sr Mgr Regulatory Affairs jobs at Teva in India, Bengaluru
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India
Bengaluru
12 jobs found
Yesterday
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Teva Mgr RA EU Generics Labeling India, Karnataka, Bengaluru
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Ensure the pharmaceutical, medical, and regulatory accuracy of English product information (SmPC, Labeling, PIL) for European procedures (MRP, DCP, CP) of innovative, biosimilar and generic products. Provide internal pharmaceutical and...
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21.07.2025
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Teva Sr Mgr Regulatory Affairs India, Karnataka, Bengaluru
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Ensure pharmaceutical, medical, and regulatory accuracy of English product information (SmPC, Labeling, PIL) for European procedures (MRP, DCP, CP) of innovative, biosimilar and generic products. Provide internal pharmaceutical and medical...
20.07.2025
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Teva Regulatory Affairs Associate III Labeling India, Karnataka, Bengaluru
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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...
30.06.2025
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Teva Sr Mgr Biostatistics India, Karnataka, Bengaluru
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Lead the development and execution of programming deliverables using RWD sources (e.g., claims, EHR, registry) to support RWE studies and analyses. Partner with RWE statisticians and cross-functional study teams to...
29.06.2025
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Teva Assoc Dir Regulatory Affairs India, Karnataka, Bengaluru
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Accountable to support all activities related to Regulatory Life Cycle Management activities in Worldwide Markets (EU, US, Other Markets: CMC Variations, Renewals, PSUR, RMP, safety variations etc). Hiring, Training and...
28.06.2025
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Teva Mgr Regulatory Affairs India, Karnataka, Bengaluru
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Carrying out dispensing activities as per applicable procedure. Responsible for recording the observation of reaction parameters on the batch card as per approve procedure. Filling of all the batch card...
19.05.2025
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Teva Sr Mgr Statistical Programming India, Karnataka, Bengaluru
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Primarily works at the product / program level. Possible to have direct reports; Likely to oversee contingent workers and/or vendors; likely to provide training to others; Analyzes needs to manage...
Description:Full job details
Ensure the pharmaceutical, medical, and regulatory accuracy of English product information (SmPC, Labeling, PIL) for European procedures (MRP, DCP, CP) of innovative, biosimilar and generic products. Provide internal pharmaceutical and...
These jobs might be a good fit
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