Regulatory Officer/Engineer

**Education**:B.PHARM;B.PHARM **Experience**:2-9 Years **Industry**: **Work Time**: **Salary**: 20000 /- Per Month **Incentive**: **Language Known**: **Phone**: +9198** URGENTLY HIRING REGULATORY AFFAIRS EXECUTIVE FOR PHARMA INDUSTRY LOCATION: BARODA (SAVLI GIDC) EDUCATION: B.Pharm / M.Pharm EXPERIENCE: Minimum 2-3 years SALARY UP TO 18,000 PM (NEGOTIABLE)...

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,...

We are looking for a highly motivated and experienced professional to join our team as an Officer / Sr. Officer Project Engineering at Lactose India Limited, located in the Pharmaceutical & Life Sciences industry. The ideal candidate should have 0-5 years of experience.Roles and ResponsibilityManage and oversee engineering projects from conception to...

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...

Require Experience : 1 Year (Solar Industry)Job Summary:The Liaisoning Officer will be responsible for handling all statutory, legal, and regulatory approvals required for solar power projects. The role involves building strong relationships with government departments, regulatory authorities, and local bodies to ensure timely clearances, compliance, and...