5.0 - 10.0 years

2 - 11 Lacs

Hyderabad / Secunderabad, Telangana, Telangana, India

On-site

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Audit Verification: Audit verified statements processed by KPO Associates, ensuring all data aligns with required standards and specifications. Mismatch Validation: Validate that any mismatches in data have been correctly identified, classified, and resolved per guidelines. Feedback & Error Handling: Provide detailed feedback on identified issues, highlighting errors or inconsistencies, and ensure timely resolution. Reporting & Recommendations: Prepare quality reports, identifying trends, issues, and process bottlenecks; recommend actionable improvements to enhance process efficiency. Compliance Adherence: Ensure that all processes comply with standard operating procedures (SOPs) and internal/external compliance guidelines. Training & Calibration: Participate in calibration and training sessions, sharing insights and helping improve team understanding of best practices and standards. Required Skills & Qualifications: Educational Background: Bachelor's degree in any discipline, Finance or Commerce preferred. Experience: Minimum of 5 years in QA or audit-related processes. Analytical Skills: Strong ability to analyze data, identify discrepancies, and apply corrective actions. Attention to Detail: High level of accuracy in validating data and identifying anomalies or inconsistencies. Documentation & Reporting: Excellent documentation skills for maintaining audit reports, quality analysis, and process improvements. Communication Skills: Strong written and verbal communication for effective feedback and reporting. Process Improvement: Ability to recommend process optimizations based on audit findings. Compliance Focused: Experience working within SOPs and compliance frameworks.

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Medical Safety Physician Diensten Tech Limited

3.0 - 8.0 years

2 - 4 Lacs

Gurgaon / Gurugram, Haryana, India

On-site

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Diensten Tech Limited is looking for Medical Safety Physician to join our dynamic team and embark on a rewarding career journey Review adverse event reports and ensure compliance with medical safety regulations Assess drug safety profiles and provide recommendations for risk management Collaborate with regulatory authorities and medical teams for patient safety Analyze clinical data to improve pharmacovigilance and adverse event reporting

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