Team Member
3 days ago
**Division**:
- Quality**Department**:
- Quality**Employment Type**:
- Permanent**Job Purpose**:
Provide healthcare professionals and patients with complete and impartial information and minimize potential risks associated with Cipla products to comply with the regulatory requirements and guarantee safety of our medical products
**Accountabilities**:
I. Provide required support for medical assessments of all products manufactured and/or marketed by Cipla to ensure regulatory compliance
II. Maintain and enhance Adverse Event (AE) guidelines to ensure the uniform and timely processing of AE reports
III. Interact with key internal/external stakeholders to continue the development of PV/DS programs (e.g., processes that meet regulatory reporting requirements)
IV. Drive activities related to label change to ensure all package updates are incorporated on time, in line with regulatory requirements
V. Drive vendor management activities to ensure vendor compliance to PV regulations
VI. Monitor the regulatory medical writing to ensure quality and good practices across reports
**Education Qualification**:
Graduate/post graduate degree in medicine (MBBS, MD, Allopathy, Lifesciences etc.)
**Relevant Work Experience**:
5 years of experience in pharmacovigilance
**Competencies/Skills**:
- Communication Skills (clarity of thought, comprehension)- Likely potential for growth- Job / Product / Technical Knowledge / Pharma domain knowledge- Presentation & Interpersonal skills (If applicable)- Managerial or People Management skills- Safety awareness (If applicable)- Relevance of Previous Experience- Comprehension, Analytical & Problem solving abilities- Productivity & Result Orientation (If applicable)- Attitude- Qualification fitment- Sales drive (If applicable)- Personality traits (Individualistic / Team player, Out spoken, Maturity level etc.)**Job Location**:
Vikhroli
**Shift Hours**:
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