Executive Regulatory Affairs

**Experience**: 0 - 5 Yrs. **Qualification**: MS-Regulatory affairs, Diploma in Regulatory Affairs, M Pharmacy, B.E Biomedical engineering, M.sc Biotechnology, M.sc Microbiology & graduation/post-graduation in any related scientific discipline **Job Profile**: As a Regulatory Affairs executive, you shall: - Prepare technical documentation for various...

Position: Regulatory Affairs Assistant - Cosmetic Industry Department: Regulatory Affairs Experience Required: 0-2 years Location: Santej, Ahmedabad Salary Range: 2.2 LPA - 3 LPA Roles & Responsibilities: 1. Handling Legal Documents and Regulatory Affairs: - Assist in the preparation, review, and submission of regulatory documents. - Maintain and...

**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. -...

Job Opening: Regulatory Affairs Executive | Vital GroupLocation: SG Highway, AhmedabadExperience: 1–3 years (Pharma Industry)Key Responsibilities:Preparation and submission of dossiers, CTD/ACTD, and regulatory documents.Handling regulatory queries and compliance requirements.Coordination with internal teams to ensure timely submissions.Support in product...

**Job Opening: Regulatory Affairs Executive | Vital Group** Location: SG Highway, Ahmedabad **Experience**: 1-3 years (Pharma Industry) **Key Responsibilities**: - Preparation and submission of dossiers, CTD/ACTD, and regulatory documents. - Handling regulatory queries and compliance requirements. - Coordination with internal teams to ensure timely...

**Job Title**: Regulatory Affairs Executive **Department**: Regulatory Affairs (RA) **Location**: Sola, Ahmedabad **Job Summary**: **Key Responsibilities**: - **Preparation and Compilation**: - Prepare registration dossiers in CTD, ACTD, or country-specific formats as per regulatory requirements. - Arrange and organize registration documents according...

Regulatory Affairs LeaderAbout the RoleWe are seeking a skilled Regulatory Affairs professional to lead our team and drive strategic growth in the medical devices industry.Key Responsibilities:Develop and implement a comprehensive regulatory compliance strategy to meet global market requirements for our products.Collaborate with cross-functional teams to...

**Introduction**: We are seeking a Regulatory Affairs Executive to join our team. In this role, you will be responsible for getting new products approval from the regulated market. In-depth knowledge of US FDA, EMA, and ICH regulatory frameworks, eCTD/ACTD dossier preparation, compilation and submission. Familiar with regulatory tools like Extedo, Lorenz,...

**Position : Regulatory Affairs Officer/Executive (Female)** **Education : B Pharm (Preferably)** **Experience : 1-2 Years** **Work Profile**: 1. Preparation & Checking of Dossiers of formulation products for product registration in other countries. 2. Co-ordination with Manufacturer & our partner in country (With their regulatory person) 3. Travel may...

About Regulatory AffairsRegulatory Affairs professionals play a vital role in ensuring the timely and successful submission of high-quality regulatory labeling submissions. They work closely with cross-functional teams, including Compliance, Marketing, R&D, engineering (packaging), manufacturing, and QA/QC.Main Responsibilities:Ensure the on-time filing of...