Regulatory Affairs Officer

**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. -...

**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...

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) -...

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...

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...

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...

**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...

**Department**: Regulatory Affairs **Designation**: RA - Officer **Education / Qualification** : B. Pharm **Experience**: 0 to 1 year **Salary**: As per company Standards **Responsibilities**: - Registering our manufacturing site in Sedex platform, completing Responsible Sourcing Policy and initiating for Smeta 4 pillar Audit from 3rd party Audit...

regulatory affairseducation: /.salary: 5 lpa to 6 lpajob location: dombivli east midcExperience5 - 6 YearsNo. of Openings3EducationB.Sc, M.ScRoleRegulatory OfficerIndustry TypePharma / BioTech / Clinical ResearchGenderMaleJob CountryIndiaType of JobFull TimeWork Location TypeWork from Office

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...