Sr Regulatory - Ahmedabad, Gujarat

This is a Regulatory Affairs position that involves developing and implementing regulatory strategies for ROW markets. · ...

We are looking for a highly skilled and experienced Regulatory Affairs / QA Validation Executive to join our team at a reputed pharma company. The ideal candidate will have a strong background in regulatory affairs and quality assurance validation. · Bachelor's degree in a releva ...

We are looking for a highly skilled and experienced professional to join our team as a Regulatory Affairs & Business Development expert. · ...

Join our team and be a vital part of ensuring regulatory excellence in the pharmaceutical industry · ...

Preparation & compilation of the dossiers in CTD/eCTD/ACTD and other formats as required for submission to different regulatory authorities. · ...

This role involves developing regulatory strategies for ROW markets, conducting regulatory landscape analysis, preparing regulatory timelines, and managing product registration processes. · ...

We are looking for a highly motivated and enthusiastic individual to join our team as a Regulatory Affairs & Business Development professional in the pharma industry. · This role is suitable for freshers with no prior experience.Strong understanding of the pharma industry and its ...

Prepare and maintain Technical Files and related documentation for medical devices. Ensure compliance with GSPR (General Safety and Performance Requirements) under EU MDR 2017/745. · ...

CTD/ ACTD · Process Validation (PV) · Stability · PDR · ...

+Job description and preparation of product permission. · +Preparation /Application of Product Permission, COPP. · Apply for FSC for products intended for export. · Ensure adherence to GMP, GLP, and regulatory guidelines of the country of registration. · ...

We are seeking a meticulous and detail-oriented Regulatory Affairs Documentation Specialist to join our team. · ...

We are looking for a Regulatory Affairs Executive who will assist in the preparation of registration dossiers handle export regulatory documentation and manage CIB & RC-related activities for agrochemical products. · Assist in preparation submission and follow-up of CIB & RC doss ...

The Regulatory Affairs Officer is responsible managing regulatory documentation and submissions in compliance with CTD dossier requirements. · ...

+Job summary · Develop and implement regulatory strategies to support research projects and product development initiatives. Monitor and interpret regulatory requirements and guidelines related to scientific research. · +QualificationsBachelors degree in a science, pharmacy, or a ...

Regulatory Affairs Associate roles involve preparing dossiers for regulatory submissions and reviewing specifications to ensure compliance with regulations. · ...

The Regulatory Affairs Manager is responsible for planning coordinating and executing regulatory activities related to pharmaceutical formulations to ensure compliance with national and international regulatory requirements. · ...

Preparation review & submission of regulatory documents ensuring compliance with guidelines supporting product approvals maintaining records coordinating with authorities. · ...

The Regulatory Affairs Manager is responsible for leading the strategic and operational aspects of regulatory submissions, approvals, and compliance across multiple markets. · ...

We are looking for a dynamic regulatory professional with a strong Food Technology background to manage USFDA compliance and regulatory liaisoning for our food division for International Business for IMPORT. · ...

Company Description · Zenith Health Science - FZCO (ZHS) is a hybrid B2B pharmaceutical venture created by industry veterans with over 25 years of experience. The company's specialty lies in launching complex generic products that face low competition in the market. · Job descrip ...