UMEDICA is a manufacturer and exporter of Pharmaceutical Formulations viz; Injectable, Tablets, Capsules, Suspensions, Dry Syrups, etc. Since our inception in 1982, we have established ourselves as a company delivering products meeting international quality standards. We are having approval of USFDA, EU, TGA and various countries viz; Zimbave, Uganda, Improving Human Health Worldwide Kenya, Ghana, ivory Coast Malawi etc.
Post : Assistant Manager in Documentation Submission Cell - Quality Assurance Department
Experience : 8 + years of relevant experience in regulated formulation pharma industry.
Qualification :- B.Pharma / M.Pharma
Salary : Budget Up to 10 Lacs
• Review of New product introduction checklist. Assurance of Availability of Documents.
• Document submission to regulatory affairs for New' ANDA submission- US /EU/CANADA.
• Document submission to regulatory affairs for new registration/ dossier filing to emerging market/ ROW market. Preventive maintenance and qualification automation.
• Query response related to ANDA/ Submission dossier. Exposure of Capacity expansion in TPM.
• To ensure the dossier filing activities , post approval changes and commitment. Introduction of New product at Umedica
Job Location : Vapi, Gujarat
Only keen interested young and dynamic Candidates, seeking opportunity to build career with rapidly growing and stable company, meeting the above-mentioned criteria may share their resume on email-id email@example.com Kindly mention the Position applied in the subject line within 4 days.
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