Job Opportunity: Senior TM : Hyderabad only : Hybrid mode !! Wissen Infotech

8.0 - 13.0 years

22 - 35 Lacs

Hyderabad

Work from Office

Responsibilities : Min 8yrs+ experienced in SAP TM (Transportation Management), BN4L-CCP, and Track & Trace. Strong experience in AMS (Application Managed Services) projects, including enhancements and bug fixes. Expertise in SAP TM configurations (Freight Orders, Planning, Tendering, Settlement). Knowledge of BN4L-CCP processes, customs compliance, and logistics document management. Experience in Track & Trace solutions, shipment visibility, and event management. Familiarity with SAP Cloud Business Network (CBN) and SAP Business Technology Platform (BTP) is a plus. Strong debugging and problem-solving skills in SAP TM and related modules. Experience in SAP integrations (IDOCs, APIs, EDI, PI/PO, CPI). Knowledge of ABAP debugging (for troubleshooting custom developments). Kindly acknowledge your interest on this Role by confirming with your updated CV. We are only looking for immediate joiners with Notice Period from 15days- 30days. If you are interested do share your updated CV at kirti_m@wisseninfotech.com

Posted 1 month ago

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Regulatory Affairs Manager in Clinical Research @ Vimta Labs Ltd, Hyd Vimta Labs

8 - 12 years

6 - 9 Lacs

Hyderabad

Work from Office

Regulatory Affairs Manager in Clinical Research @ Vimta Labs Ltd, Hyd Experience: 8-12 years of Regulatory Affairs experience in Clinical Research Industry. CTC: Based on their current CTC. Job Description Regulatory Affairs Manager Primary Responsibilities: 1.. Manage the activities of Regulatory Affairs for clinical research and ensure the implementation of effective regulatory strategies. 2. CDSCO, CBN and NCB getting approvals as required for Vimta. 2. Provide regulatory input to strategic decision making; including prioritization, and external communications 3. Provide regulatory input to in-licensing evaluations and due diligence activities 4. Provide advice about regulations to manufacturers/scientists 5. Coordinate successful submissions and approval of all applications 6. Ensure that quality standards are met and that the deliverables meet strict deadlines and fulfil applicable regulatory and quality standards. 7. Plan, undertake and manage regulatory inspections 8. Keep up to date with national and international guidelines and customer practices 9. Develop and establish standard operating procedures that convey the best practices in the company 10. Collect, collate, and evaluate scientific data from a range of source. 11. Monitor and set timelines for licence variations and renewal approvals 12. Ensures that Good Clinical Practices (GCP) are followed. 13.Responding to any quality & regulatory issues related to clinical department and taking relevant corrective and preventive actions Secondary Responsibilities: 1. Ensure Quality Control review of protocols, ICF, CRF protocol amendments, Clinical Trial Reports, Investigator Brochures and regulatory submission documents. 2. Interpretation of data. 3. Preparation and Review of Clinical Study Report Interested candidates can share their resumes to keerthana.rojanala@vimta.com Contact: Keerthana

Posted 2 months ago

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