Regulatory Documentation

This is a full-time on-site role as a Junior Regulatory Affairs Executive located in Noida. The Junior Regulatory Affairs Executive will be responsible for regulatory documentation, ensuring compliance with regulatory requirements, preparing dossiers, and managing regulatory affairs. **Qualifications**: Regulatory Documentation, Regulatory Requirements, and...

**Role Description** This is a full-time on-site role as a Junior Regulatory Affairs Executive located in Noida. The Junior Regulatory Affairs Executive will be responsible for regulatory documentation, ensuring compliance with regulatory requirements, preparing dossiers, and managing regulatory affairs. **Qualifications** - Regulatory Documentation,...

**JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

The Document Controller will be responsible for managing and maintaining project folders, updating company documents, and ensuring proper tracking of all created documents. This role plays a critical part in ensuring that all project-related documentation is well-organized, easily accessible, and up-to-date to support smooth project execution. **Key...

**4PL Consultancy is a London Based Logistics and Supply Chain Management Consultancy** We are a young and creative company, and we offer you fresh Logistics & Trade Compliance ideas. 4PL Consultancy is a fourth party Logistics and Supply Chain Management solution provider from Crawley, West Sussex. Our sole aim is to bring efficient upgrades to the supply...

**Job Title**: Export Documentation Executive **Location**: Noida, Uttar Pradesh, India **Company**: San Dee Impex **About the Role** San Dee Impex seeks an **Export Documentation Executive** to handle all documentation processes related to export operations. This role involves managing Export LC, banking, shipping, purchasing, and general office...

Job Description: - CDSCO Registration for medical devices, Drug & Cosmetics as per the rules and standards. - Draft, review, submission and archival of other regulatory submissions (Query responses, corrections fillings, miscellaneous notifications regarding post registration regulatory lifecycle management) for Indian market. - Review of technical...

A) About the RoleMercados requires a skilled and experienced Regulatory Support Consultant to provide comprehensive support in handling various day-to-day and routine regulatory matters related to regulatory bodies and other authorities such as UPERC, CERC, MOP, MNRE, CEA and GoUP.B) Detailed expectations from the rolePetition Filing and Compliance:-...

A) About the RoleMercados requires a skilled and experienced Regulatory Support Consultant to provide comprehensive support in handling various day-to-day and routine regulatory matters related to regulatory bodies and other authorities such as UPERC, CERC, MOP, MNRE, CEA and GoUP.B) Detailed expectations from the rolePetition Filing and...

**Documentation Preparation**: Prepare and review all necessary shipping documents, including bills of lading, packing lists, commercial invoices, certificates of origin, and any other required documentation. - **Regulatory Compliance**: Ensure all documentation complies with international shipping regulations, customs requirements, and company policies. -...

**Documentation Preparation**: Prepare and review all necessary shipping documents, including bills of lading, packing lists, commercial invoices, certificates of origin, and any other required documentation. - **Regulatory Compliance**: Ensure all documentation complies with international shipping regulations, customs requirements, and company policies. -...

Regulatory Affairs Specialist Careers that Change Lives Collaborate and partner with Design QA, R&D, Sustaining Engineering, Clinical Affairs, Marketing and Operations. Supports the Global Operating Unit Regulatory Affairs function as the local representative for ensuring requirements are met. Responsible for supporting the needs of the MEIC with regulatory...

**JOB DESCRIPTION** **Executive-Documentation **Roles & Responsibilities** The Executive, Documentation will be responsible for managing and overseeing all documentation processes related to the manufacturing operations within the ATL Primary Metals function at ATL. This role involves ensuring the accuracy, completeness, and accessibility of production and...

**Description** Drug Regulatory Affairs - Job description - Prepare CTD, ACTD Dossiers and file regulatory submissions. - Perform assessments of new or revised products. - Manage complaint documentation (including investigation and closure). - Respond to inquiries from regulatory bodies. - Should be technically well versed with requirements for medicines...

Hii Connection We are Looking for Export Documentation About the Role: The Export Documentation and Coordination Specialist will be responsible for ensuring the smooth and efficient execution of export orders. This role involves liaising with various regulatory bodies such as Banks, Customs, DGFT, and UPEPB, and coordinating with internal departments...

**JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

**JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

**JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

**JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

**Job Title**: AERB Regulatory Compliance Officer **Job Summary**: As an AERB Regulatory Compliance Officer, you will be responsible for overseeing and ensuring compliance with regulatory requirements established by the Atomic Energy Regulatory Board. Your role will involve collaborating with various departments within nuclear facilities to assess, monitor,...