Executive Regulatory

**Executive Regulatory Affairs (API Pharma)** **Qualification**: M.Sc. - Organic & preferably diploma or must have worked in Regulatory Affairs department of Pharmaceutical Organization / API **Experience** : 8 - 10 years in Quality Assurance department (QA) of Pharmaceutical Industry & regulatory Affairs department ,preferably from API Pharma industry. -...

Regulatory Executive (Female)/ Dombivli - Mumbai Pharmaceutical Thane, Dombivli Share VACANCY REGULATORY AFFAIRS EXECUTIVE (Pharma Company is manufacturing veterinary products) Job Location: Mumbai Maharashtra Eligibility: - M. Sc / B. Sc / M. Pharm / B. Pharm. Degree / Diploma in Regulatory Affairs. - Should have good knowledge of preparing...

**Department**: Regulatory Affairs **Designation**: Executive **Education / Qualification**: B. Pharm **Experience**: 3 to 5 year **Salary**: As per company Standards **Responsibilities**: - Data compilation, Preparation of DCP, EDMF, CEP, and Drug Master File (DMF)/Formulation Dossier related to other countries as per marketing department requirement...

Regulatory Affairs Executive (female)/ Palghar East Thane, Palghar Share VACANCY REGULATORY AFFAIRS EXECUTIVE (Pharma Company is manufacturing veterinary products) Job Location: Palghar East Maharashtra Eligibility: - M. Sc / B. Sc / M. Pharm / B. Pharm. Degree / Diploma in Regulatory Affairs. - Should have good knowledge of preparing registration of...

Handling dossier, COPP submission and query Handling for South East Asian Country, East Africa, Latin America, Central America, Europe. - In depth knowledge about regulatory requirements for above region - Need to work independently - Need to have knowledge about legal documents requirement and it’s processing. - New customer development and new business...

Review and interpret applicable regulations and guidelines - Manage and ensure the accuracy of regulatory documents - Monitor and respond to changes in the regulatory environment - Develop and maintain strong working relationships with relevant stakeholders - Participate in internal and external audits - Keep up to date with developments in the regulatory...

We are looking for young and enthusiastic minds, who will be responsible for the following roles - 1. Preparation and compilation of CTD and ACTD dossiers for Vietnam, Myanmar and ROW market 2. Review of Process Validation, Analytical Method Validation, Product Development Records, BMR, BPR, Stability data, Certificate of Analysis etc. required for...

**Documentation: Related all to QA, TM etc** **Logistic: Direct enquiry for product from Consumer/Clients** **Communication: Related to project/sample requirement.** **Others: 1.Updation and checking GS1 data kart.** **2. Fssai/FoSCOS updation/tracking for license/ renewal -** **Salary**: ₹12,000.00 - ₹18,000.00 per month Schedule: - Day...

Preparation of dossier sections for EU/Australia/Canada/Emerging market. - Variation filing in above markets - Artwork management - Review of analytical documents - Review of QMS documents

**Job Title**: Europe & Scandinavia Operations Executive **Department**: International Operations / Regional Management **Reports to**: Regional Operations Manager / Director of International Operations **Location**: [Company HQ or regional office] **Employment Type**: Full-time **Job Summary**: The Europe & Scandinavia Operations Executive is responsible...