Regulatory Affairs Executive

Job Description:Regulatory Affairs Officer (RA)Qualification: B.Pharm/ M.PharmExperience: Minimum 3 years in regulatory affairs for the ROW (Rest of the World) market, with a total of 3 to 5 years of experience.Job Description:Preparing dossiers as per country-specific guidelines.Compiling and reviewing documents.Coordinating with QA for...

**Title**:Executive - Regulatory Affairs**: - Date: Jul 4, 2025 - Location: Tandalja - R&D - Company: Sun Pharmaceutical Industries Ltd - Preparation, reviewing, timely submission and coordination of implementation of labeling based on FDA notifications and/or RLD labeling updates. - Coordination of labeling related activities with cross functional teams...

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...

**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...

Job TitleExecutive – Regulatory AffairsBusiness UnitR&D1 Regulatory AffairsJob GradeG12ALocationBarodaAt Sun Pharma, we commit to helping you "Create your own sunshine"— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.Are You Ready to Create Your Own Sunshine? As you enter the Sun...

Job Description:works to help a company or organization meet all state, local, federal, international, and industrial regulations that apply to their products.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...

**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...

Role & responsibilitiesResponsible for Drug Master Filing submissions to various regulatory agencies like USFDA, European Agencies, Brazil, and other semi-regulatory countries.Review and submission of Response to queries raised on DMF by USFDA, and other agencies.Review and submission of Amendments and revisions of Drug Master Files.Review and ensuring the...

**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...