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...

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,...

**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...

**Vega Biotec Pvt Ltd** a part of Vega group of companies having global presence and state of the art manufacturing pharmaceutical factory is having an opening for the following post. Qualification - B.Pharm/ M. Pharm Experience - 3+ years of experience in regulatory affairs for ROW market (Rest of the world) **Job Summary**: The Regulatory Affairs...

Studying scientific and legal documents - Gathering, evaluating, organising, managing and collating information in a variety of formats - Ensuring compliance with regulations set by the Medicines and Healthcare products Regulatory Agency (MHRA) - Maintaining familiarity with company product ranges - Planning, undertaking and overseeing product trials and...

Role Objective Key objective of this role is to prepare, review, and maintain regulatory documents in compliance with international standards and country-specific requirements. The role ensures timely preparation and updating of Technical Master Files, supports product registrations, manages post-market surveillance activities, and contributes to audit...

**Description**: - They must have excellent organizational, analytical, project management, and communication skills. - They work frequently with other employees and team members to coordinate complex activities, often with competing priorities. - Most regulatory affairs positions are full time. - Regulatory Responsibility means a duty or responsibility,...

Preparation of DMFs for different markets in CTD and eCTD formats.Coordination with cross-functional dept to manage the documents.Supporting marketing team & QC/QA/R&D in various capacity.Preparation of Declarations and other supporting docs. Required Candidate profileCandidate from Pharma - API industry and should have 8+ Years of Experience in Regulatory...

**Role & 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...

**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...