Position Name: Regulatory Affairs Associate II
Company Name: Teva Pharmaceuticals
Department: Regulatory Affairs
Qualification: Graduation/Post-Graduation in Science/Pharma Discipline
Experience: Minimum 3 years of core pre-approval regulatory activity experience
Job Location: Goa, India
Description:
Teva Pharmaceuticals seeks a Regulatory Affairs Associate II in Goa. Ensure regulatory compliance and support submissions.
Responsibilities:
Key Responsibilities |
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Assess submission documentation for compliance |
Coordinate with external parties and cross-functional teams |
Compile CMC dossier for EU and other filings |
Support due diligence processes and address deficiencies |
Handle deficiency letters from regulatory authorities |
Escalate key issues to management |
Assist submissions team with administrative tasks |
Experience and Qualifications:
- Graduation/Post-Graduation in Science/Pharma Discipline.
- Minimum 3 years of core pre-approval regulatory activity experience in EU and allied markets.
- Reports To: Sr. Manager – Regulatory Affairs
Equal Employment Opportunity Commitment:
Teva Pharmaceuticals is committed to equal opportunity in employment. We foster a diverse and inclusive workplace for all.
Meta Description:
Join Teva Pharmaceuticals in Goa as a Regulatory Affairs Associate II. Ensure compliance and support regulatory submissions. Apply now!