Regulatory Officer

- Regulatory Officer for Medical Devices - DMF submission for US, Health Canada, EU, India, China and other countries as per requirements - Indian MDR (CDSCO) license applications - Maintain regulatory documentation for all input materials received from suppliers - USP testing & Biocompatibility testing of products to maintain - Post Market Surveillance of...

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...

**Industry: - Pharmaceutical** **Experience: - 1 to 3 years** **To assist in obtaining and maintaining government approval for drugs, medical devices, nutritional products, and related materials**. - 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...

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,...

Job Description:Job responsibilities are to Assist Regulatory manager:Preparation, Compilation and review of registration dossier of tablet /capsule/injection in CTD,ACTD as well as country specific format for countriesPreparation, Compilation and review of registration dossier of capsule/syrup/balm in a Herbalproducts for country specific format in...

**Qualification : M.pharm** **Experience : 1-4 years Europe Submission Preference** - **studying scientific and legal documents to check they meet legal requirements.**: - **gathering, evaluating, organising, managing and collating information in a variety of formats.**: - **submitting information and responding to queries from bodies such as the...

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...

Location: India – Office based in Anand, Vadodara :Salary: Dependent on ExperienceWorking Pattern: Full-time, Monday–Friday 9am – 5.30pm, but would have regular UK communications and other markets, so flexibility is keyReports to: COOAbout UsWe are a UK based Food Supplement Company, who is both UK and export-focused with a growing global footprint. We...

**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...

Job Title Senior Executive Manager 2 - Regulatory Affairs Business Unit R D1 Regulatory Affairs Job Grade G11A G11B Location Baroda At 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...