Regulatory Affairs Cdsco

Company OverviewEnterslice, a leading provider of regulatory solutions, is seeking an experienced Regulatory Affairs Specialist to join our team. Our company is dedicated to driving regulatory excellence and compliance in the healthcare and cosmetic sectors.Job SummaryWe are looking for a highly skilled Regulatory Affairs Specialist with expertise in CDSCO...

Job Title: Manager – Regulatory Affairs (CDSCO) Location: Sector-60, Noida Company: Corpbiz ( A unit of Enterslice Private Limited) Job Description: We are seeking an experienced Manager – Regulatory Affairs specializing in CDSCO compliance and related regulatory domains. The ideal candidate will handle end-to-end documentation,...

**Responsibilities**: - Maintain Daily project report. - Handling end-to-end filing, Document upload, document preparations and device master plan preparation - Manage customer relationships through regular communication with clients through weekly/ monthly reviews. - Discuss operational issues and critical to quality (CTQ) delivery issues with the...

OverviewEnterslice, a dynamic regulatory consulting firm, is seeking an experienced Regulatory Affairs expert to join our team in Noida. As a key member of our team, you will play a crucial role in ensuring compliance with CDSCO regulations and related domains.About the JobAs Regulatory Affairs Expert, you will handle end-to-end documentation, submission,...

At Enterslice, we are seeking a seasoned Regulatory Affairs Specialist to join our dynamic team in Noida.Job Summary:We are looking for an experienced professional with expertise in CDSCO filings and regulatory submissions to handle licenses for Medical Devices, IVDs, and Drugs. The ideal candidate will have a strong understanding of ISO standards and Indian...

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...

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...

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...

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...

Regulatory affairs professionals play a critical role in the drug development process, working closely with other stakeholders to ensure that pharmaceutical products meet regulatory requirements at every stage of development. Some of their key responsibilities include ( CTD/ ACTD DOSSIER PREPRATION ( MARKET ASEAN, CIS ROW ) **Regulatory Strategy...

**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...

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...

**Company Description** Technoledge is an educational institution located in Noida. Our primary objective is to provide support for the development, coordination, implementation, and planning of educational programs. We offer a wide range of services including smart hybrid schools, engineering services, manpower solutions, skill development, e-learning...

Job Title: Regulatory Affairs ManagerEstimated Salary: ₹1,200,000 - ₹1,800,000 per annumAbout the Role:We are looking for an experienced Regulatory Affairs Manager to join our team at Paytm Payments Bank. As a key member of our regulatory affairs team, you will play a crucial role in ensuring that our business operations comply with relevant laws and...

**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...

**About Company** **Pharma Regulatory Institute (PRI)** This is a project (PRI) of Accredited Consultants Pvt. Ltd. (ACPL), Noida who are very well established in the business of Regulatory Affairs and Pharmacovigilance for the last 25 years and created a very strong image in the industry. ACPL clients are widely distributed in Foods, Pharmaceuticals,...

**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...

**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,...