Regulatory Affairs Executive

**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 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...

**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 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...

As a regulatory affairs officer, you'll need to: - ensure that a company's products comply with the regulations of the regions where they want to distribute them - keep up to date with national and international legislation, guidelines and customer practices - respond to queries from medical bodies like Healthcare products Regulatory Agency (MHRA) -...

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...

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...

Compilation of Dossier in CTD/eCTD format, Preparation of SOPs, Helping In QA Audit, Technical document Preparation, Good Written And Communication Skills, Reviewing of Technical Documents. Jobs available after training & certification under govt. accreditation of LSSSDC. **Responsibilities and Duties** Compilation of Dossier in CTD/eCTD format, Preparation...

**Job description** - Reviewing, Compilation, Preparation of Registration Dossiers CTD, ACTD & country specific Dossiers as per country's guidelines. - Handling registration queries, Developing samples for registration. - Review of technical documents like, specifications, Certificate of Analysis, Method of Analysis, Test Methods, Testing Reports, Stability...

**Regulatory Affairs**: Ø **Regulatory Compliance**:Ensure that the company's products are in compliance with local and international at all stages of development, manufacturing, and post-market. Maintain awareness of updates to regulations and inform the team as necessary.Ø **Labeling and Documentation**:Review product labeling and packaging for...