Senior Officer, Regulatory Affairs - Ahmedabad
3 weeks ago

Job description
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Access all high-level positions and get the job of your dreams.
Similar jobs
Il responsabile dei rapporti regolamentari sarà coinvolto in una serie di attività per garantire il rispetto delle normative vigenti. · CTD/ ACTD · Process Validation (PV) · Stability · ...
1 month ago
We are looking for a highly skilled and experienced professional to join our team as a Regulatory Affairs & Business Development expert. · ...
3 weeks ago
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 ...
3 weeks ago
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 ...
3 weeks ago
**Vivanza Biosciences Limited** is seeking a highly motivated and detail-oriented professional to join our team as a **Regulatory Affairs Executive** in Ahmedabad, Gujarat. This role is ideal for an individual with foundational experience in the pharmaceutical industry who is kee ...
14 hours ago
Responsibilities: · Dossier Preparation: · Compile, review, and prepare regulatory documentation, ensuring accuracy and completeness. · Collaborate with cross-functional teams to gather necessary information for dossier submissions. · Maintain and update regulatory files and data ...
17 hours ago
Experience: · Total of 10 to 15 years in Regulatory Affairs (RA). · At least 6 years of experience in regulated markets such as the USA, EU, UK, or CA. · Multiple market experience is an advantage. · Skills: · Excellent written and verbal English communication skills. · Proven ...
3 days ago
CTD/ ACTD · Process Validation (PV) · Stability · PDR · ...
1 week ago
Preparation & compilation of the dossiers in CTD/eCTD/ACTD and other formats as required for submission to different regulatory authorities. · ...
1 month ago
This is a Regulatory Affairs position that involves developing and implementing regulatory strategies for ROW markets. · ...
1 week ago
+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. · ...
1 month ago
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. · ...
1 month ago
Regulatory Affairs Associate roles involve preparing dossiers for regulatory submissions and reviewing specifications to ensure compliance with regulations. · ...
3 weeks ago
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. · ...
4 weeks ago
Preparation review & submission of regulatory documents ensuring compliance with guidelines supporting product approvals maintaining records coordinating with authorities. · ...
1 month ago
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 ...
1 month ago
Qualification : Postgraduate or equivalent in Pharma/Medical Devices domain · Reports to: Head of RA / RA Manager · About the role: · We are seeking experienced candidates to join our dynamic team in the Quality Assurance / Regulatory affairs, in the field of class III / class ...
3 days ago
The Regulatory Affairs Manager is responsible for leading the strategic and operational aspects of regulatory submissions, approvals, and compliance across multiple markets. · ...
3 weeks ago
Determining the appropriate risk class of a device, developing a strategic pathway for device approval or clearance in target markets and identifying applicable guidelines and monitoring compliance. · Drafting Instructions for Use (IFU), labels, implant cards, and other applicabl ...
1 week ago
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. · The role involves handling product approvals, regulatory submissions, ...
1 month ago
Collaborate with cross-functional teams on product launches Ensure compliance with regulatory requirements Prepare dossiers for pesticide registrations Manage regulatory affairs portfolioCollaborate with cross-functional teams on product launches · Ensure compliance with regulato ...
1 month ago