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25 jobs found for Ayusearch Drugs & Laboratories

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  • with medical and therapeutic terminology. Ability to work independently but guided by documented procedures, with appropriate support. Able to work effectively as part of a team. Understanding of patient safety regulatory obligations. Should be familiar with regulatory & pharmacovigilance guidelines. Should

  • with medical and therapeutic terminology. Ability to work independently but guided by documented procedures, with appropriate support. Able to work effectively as part of a team. Understanding of patient safety regulatory obligations. Should be familiar with regulatory & pharmacovigilance guidelines. Should

  • with medical and therapeutic terminology. Ability to work independently but guided by documented procedures, with appropriate support. Able to work effectively as part of a team. Understanding of patient safety regulatory obligations. Should be familiar with regulatory & pharmacovigilance guidelines. Should

  • with medical and therapeutic terminology. Ability to work independently but guided by documented procedures, with appropriate support. Able to work effectively as part of a team. Understanding of patient safety regulatory obligations. Should be familiar with regulatory & pharmacovigilance guidelines. Should

  • with medical and therapeutic terminology. Ability to work independently but guided by documented procedures, with appropriate support. Able to work effectively as part of a team. Understanding of patient safety regulatory obligations. Should be familiar with regulatory & pharmacovigilance guidelines. Should

  • and Skills: Basic competence with medical and therapeutic terminology. Ability to work independently but guided by documented procedures, with appropriate support. Able to work effectively as part of a team. Understanding of patient safety regulatory obligations. Should be familiar with regulatory &

  • and Skills: Basic competence with medical and therapeutic terminology. Ability to work independently but guided by documented procedures, with appropriate support. Able to work effectively as part of a team. Understanding of patient safety regulatory obligations. Should be familiar with regulatory &

  • and Skills: Basic competence with medical and therapeutic terminology. Ability to work independently but guided by documented procedures, with appropriate support. Able to work effectively as part of a team. Understanding of patient safety regulatory obligations. Should be familiar with regulatory &

  • and existing product improvements from regulatory perspectives. Art work review, license review and approval of drug products. FDA and CDSCO Notices replies for not of standard quality complaints. Follow up for the resolution of the NSQ complaints. Coordination with the medical department for drafting

  • and existing product improvements from regulatory perspectives. Art work review, license review and approval of drug products. FDA and CDSCO Notices replies for not of standard quality complaints. Follow up for the resolution of the NSQ complaints. Coordination with the medical department for drafting

  • activities. OTHER RESPONSIBILITIES: Following up with sites regarding outstanding queries. Follow up on reconciliation of discrepancies. Follow departmental AE workflow procedures Closure and deletion of cases Perform any other drug safety related activities as assigned Perform literature review activities

  • activities. OTHER RESPONSIBILITIES: Following up with sites regarding outstanding queries. Follow up on reconciliation of discrepancies. Follow departmental AE workflow procedures Closure and deletion of cases Perform any other drug safety related activities as assigned Perform literature review activities

  • activities. OTHER RESPONSIBILITIES: Following up with sites regarding outstanding queries. Follow up on reconciliation of discrepancies. Follow departmental AE workflow procedures Closure and deletion of cases Perform any other drug safety related activities as assigned Perform literature review activities

  • requirement. 2. Must understand the pharmacokinetics of drugs. 3. working knowledge of cGMPs, Standard Operating Procedures, FDA regulations and safety. 4. To draft a strategy document outlining a road map for the Project under development and monitor the same during execution phase. 5. To complete

  • requirement. 2. Must understand the pharmacokinetics of drugs. 3. working knowledge of cGMPs, Standard Operating Procedures, FDA regulations and safety. 4. To draft a strategy document outlining a road map for the Project under development and monitor the same during execution phase. 5. To complete

  • requirement. 2. Must understand the pharmacokinetics of drugs. 3. working knowledge of cGMPs, Standard Operating Procedures, FDA regulations and safety. 4. To draft a strategy document outlining a road map for the Project under development and monitor the same during execution phase. 5. To complete

  • requirement. 2. Must understand the pharmacokinetics of drugs. 3. working knowledge of cGMPs, Standard Operating Procedures, FDA regulations and safety. 4. To draft a strategy document outlining a road map for the Project under development and monitor the same during execution phase. 5. To complete

  • requirement. 2. Must understand the pharmacokinetics of drugs. 3. working knowledge of cGMPs, Standard Operating Procedures, FDA regulations and safety. 4. To draft a strategy document outlining a road map for the Project under development and monitor the same during execution phase. 5. To complete

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