Regulatory Affairs Officer

URGENT OPENING FOR REGULATORY AFFAIRS OFFICER/ SR OFFICER LOCATION VADODARA Position:-Regulatory Affairs Officer/ Sr OfficerLocation:-VadodaraExperience:-1 to 3 Yrs (Formulation)Qualification :- B.Pharm/ M.Pharm Required Candidate profilePreparing dossiers as per country-specific guidelines.Compiling and reviewing documents.Coordinating with QA for...

**Position**: Regulatory Affairs Specialist **Location**: Odhav. Ahmedabad **Department**: Regulatory Affairs **Reports to**: Regulatory Affairs Manager / Director Job Summary: Key Responsibilities: - **Compliance Monitoring**: Monitor changes in regulations and guidelines to ensure ongoing compliance with local and international regulations. -...

Good communication and teamwork abilities. - Basic understanding of **regulatory affairs** in the pharmaceutical industry. - Strong **documentation and organizational skills**. - Knowledge of **CTD/eCTD submissions** is a plus. - Assist in the **preparation and submission of regulatory documents**, including dossiers for product registrations, variations,...

ResponsibilitiesAs a regulatory affairs officer:ensure that a company's products comply with the regulations of the regions where they want to distribute themkeep up to date with national and international legislation, guidelines and customer practicesrespond to queries from medical bodies like the Medicines and Pertaining to that Guidelines.collect, collate...

**Regulatory Affairs Executive Job Description** **Job Summary**: The Regulatory Affairs Executive will work with product development and manufacturing management to ensure that the product development process meets all applicable regulatory requirements. **Duties/Responsibilities**: - Works in the regulatory affairs department on assigned projects. -...

**Post**: RA Executive **Experience**: 5+ Years Experience in Regulatory Affairs in Pharma Industry (Formulation) **Location**: Vadodara - Experience in handling regulatory affairs for ROW market mainly Central and Latin American, African & Asian countries for Pharma Formulations. - Preparation, Compilation & Review of Registration documents that include...

**Roles and Responsibilities** - EU Dossier preparation and submission to Europe market - EU ASMF and CEP preparation and submission to Europe with post approval activities - Handling of EDQM Agency Queries - Brazilian DMF Preparation and Deficiency response - China DMF Preparation and Deficiency response - eCTD publishing in EDUCE software with PDF...

**Qualification**: B.Pharma - Pharmacy or M.Pharma - Pharmacy **Experience**: 2.0 Year **To** 4.0 Year **( Must have experience in Pharma Formulations)** 1. Preparing dossiers as per country specific guidelines 2. Countries knowledge - Africa, South East Asia They must have excellent organizational, analytical, project management, and communication...

Position Regulatory Affairs Associates Location - Vadodara KRA: As a RA Sr. Officer Reviewing artwork, PRAC variations, CEP updates for EU market. Preparation of Regulatory Strategic documents for EU/UK market. Review and compilation of deficiencies response for ROW (specially MENA, LATAM market) Compilation and submission of renewal, variation for...

**Title**:Executive - Regulatory Affairs**: - Date: Sep 26, 2025 - Location: Tandalja - R&D - Company: Sun Pharmaceutical Industries Ltd **Job Title**: Executive - Regulatory Affairs **Business Unit**: R&D1 Regulatory Affairs **Job Grade** G12A **Location** Baroda At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering...