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Quality Review & Regulatory Report Submission

Quality Review & Regulatory Report Submission

Vizen Life Sciences

4 - 6 years

2 - 6 Lacs

Hyderabad

Posted:2 months ago| Platform:

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Skills Required

Analytical skills Manager Quality Assurance Compliance Regulatory reporting Time management Database Pharmacovigilance Case processing Quality Review

Work Mode

Work from Office

Job Type

Full Time

Job Description

To Approve schedule the reports in Argus database to the respective health authorities as applicable Submission of cases to Health Authorities, Business partners and Affiliates as applicable Adherence to internal and external timelines for case processing to maintain regulatory reporting compliance To schedule and approval of regulatory reports based on reporting obligations. Job Requirements: Years of Experience: 4-6 years of relevant experience in Pharmacovigilance (PV), specifically in ICSR Quality Review and Regulatory Report Submissions. Hands-on experience with the Argus Database is essential. Educational Qualification: B.Pharm, M.Pharm. Skills and Competencies: Strong knowledge of PV regulations and guidelines for health authority submissions. Expertise in quality assurance and compliance. Excellent attention to detail and analytical skills. Effective communication and time management abilities

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Vizen Life Sciences

www.vizenlifesciences.com

Biotechnology

San Francisco

50-100 Employees

11 Jobs

Key People

Dr. Alice Johnson

CEO
Mark Smith

CTO

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