Regulatory Affairs Executive

Job Title - Regulatory Affairs Experience - 3 -5 years in finished doses form Location - Pune Industry - Leading Pharma Industry Roles and Responsibilities To coordinate and preparation of Quality Agreements. Maintain the required documents for Regulatory Affairs. Liaising with customers and regulatory authorities regarding quality matters, including...

Job Title Regulatory Affairs Specialist Job title Regulatory Affairs Specialist Your role Be recognized as a key talent in International Regulatory filings and procedures Be considered a key regulatory point person in Centralization of Regulatory Operations and enable the regulatory compliance in Markets where Philips products are commercialized ...

The **Regulatory Affairs Specialist** stays with the same company for an average of 10 to 15 years; the rate of turnaround is therefore low. Networking is very much encouraged, through joining various associations to participate in conferences and exhibitions, and also to access current literature. Presently, there is a strong demand for Regulatory Affairs...

Designation : Regulatory Affairs Specialist - Qualifications : Bachelor's degree in a scientific discipline, such as pharmacy, biology, or chemistry - Experience : Minimum 2-5 years of experience in regulatory affairs - Salary : Good Hike on Current CTC - Location : Sandhurst Road Mumbai - Head

_**Duties/Responsibilities**:_ - Works in the regulatory affairs department on assigned projects. - Coordinates with product development and/or research and development teams to request, develop, and prepare required data and reports to be submitted to regulatory bodies and agencies. - Collaborates with key staff from Planning, Product Development,...

At Ultratech India Limited, we believe employees are at the heart of all that matters. Connected in purpose by career, life, and health. The best people produce the best products and thus Ultratech is constantly on the lookout for bright and ambitious team players who have a strong commitment towards the organization. **Regulatory Affairs Executive**: ...

**Job Summary**: We are seeking a highly skilled Regulatory Affairs Specialist to join our team. The requirements for our products, managing the submission process for regulatory approvals, and maintaining up-to-date knowledge of regulatory changes. Essential Duties and Responsibilities: **Regulatory Compliance**: Ensure company products comply with...

Job Description: As a **Medical Device Regulatory Affairs Intern**, you will work alongside experienced regulatory professionals, gaining hands-on experience in regulatory submissions, compliance research, and documentation for medical devices. Key Responsibilities: - Assist in preparing regulatory documentation for product registrations and submissions. -...

Please find JD for Regulatory Affairs (ROW Market formulation): 1. Preparation of Dossier in CTD, ACTD and country specific format. 2. Resolving queries received from various Ministry of Health. 3. Preparation of Technical master file for Medical Device. 4. Finalization of Artwork as per Country specific guidelines. 5. Co-ordination with vendors for DMF...

Job Title: Senior Executive - Regulatory Affairs UK/IE/MT Department: Regulatory Affairs Grade Level: P-2 Reports to: Manager / Sr. Manager - Regulatory Affairs Number of Reports: NONE Location: Mumbai **Main purpose of role**: To ensure adequate and prompt life cycle maintenance activities for Marketing Authorization’s (MA) held based on portfolio...