Avantika Medex Pvt. Ltd. is a leading pharmaceutical company based in Ahmedabad, Gujarat, India. Established in 2007, the company specializes in manufacturing, exporting, and wholesaling high-quality pharmaceutical products.
Avantika Medex requirement details:
Designation: Senior Officer
Department: Regulatory Affairs
Qualification : B.Pharm/M. Pharm
Experience: 3-4 years.
Job Responsibilities
1. Dossier Preparation in CTD/ACTD/Country Specific Formats
2. Re-registration and Renewal Application
3. Variation Application
4. Queries Handling
5. DMF Activity
6. Artwork Review (Carton/Foil/Label/Insert/Shipper)
7. Pack insert Preparation as per Country Guideline
8. Documents and Sample Collection Activity from F&D, QA, QC and Store department for registration requirements.
9. Documents Review Knowledge: Pharmaceutical Development Report, Process Validation Protocol & Report, Excipients Specifications/MOA, Finished Product Specification/MOA, Packing Material Specification/MOA, COA, Stability Study Protocol & Report, MFR, BMR, BPR, Clinical/Non Clinical Literature Search Strategy, AMV, CDP, BE Study.
Country Experience Required: Kazakhstan, Azerbaijan, Turkmenistan, Philippines, Vietnam and Myanmar.
Dosage Form Experience Required:
Tablets, Capsules, Oral Powder (Sachet), External Preparation (Gel & Cream), Injections, Infusions.
Walk in interview details:
Candidates can also share their resumes on the mentioned email id: branding@avantikamedex.com
INTERVIEW VENUE
1308, Shapath V Nr. Crown Plaza Hotel, S.g Highway Vejalpur, Ahmedabad-380051, Gujarat, India.
Walk in date : 09 January, 2025
Time: 11:30am to 3:00pm
+91 96248 49118
www.avantikamedex.com
