Drug & Cosmetic - Regulatory Affairs

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,...

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,...

**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...

**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...

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...

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...

Lucent Biotech Limited company Hiring For **Drug Regulatory Affairs Executive.** **Regulatory affairs officers ensure the appropriate licensing, marketing and legal compliance of a range of pharmaceutical and medical products in order to control their safety and efficacy** As a regulatory affairs officer you'll be the crucial link between your company, its...

Lucent Biotech Limited company Hiring For **Drug Regulatory Affairs Executive.** **Regulatory affairs officers ensure the appropriate licensing, marketing and legal compliance of a range of pharmaceutical and medical products in order to control their safety and efficacy** As a regulatory affairs officer you'll be the crucial link between your company, its...

**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...

**Responsibilities**: - Take regular classes as and when assigned by the HOD - Be regular and punctual in taking the classes of theory as well as Hands on training. - Instruct all the students to attend the classes regularly - Conduct regular internal tests for the students - Submit the list of students absent for the internal tests and reported to the...

Hii Seekers, CORPSEED is looking for Management Trainee - Regulatory Affairs || CDSCO Role. Location - Noida Experience - 6 months to 2 Yrs Corpseed ITES Pvt. Ltd. is a technology platform, make things easier for Entrepreneurs and businesses. Just like a seed is required to grow a tree similarly, there are few prerequisites like “Business Planning,...

**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 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...

**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...

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...

**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,...