Drug & Cosmetic - Regulatory Affairs

**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...

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,...

Clinical Affairs ManagerJoin the Future of HealthcareTC4A, a pioneer in democratizing healthcare innovations, is revolutionizing diagnostics with LightAI. We are seeking talented individuals to join our office in Noida and address one of healthcare’s biggest challenges, the overuse of antibiotics that leads to drug-resistant infections and costs billions...

**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...

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: - Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø A Bachelor’s/ Master degree in B. Pharma / M. Pharma Ø Perform assessments of new or revised products Ø Experienced with 1 Yrs should apply. Ø Good Communication skills Job Type-Fulltime contact no-8810226562 Pay: ₹15,000.00 - ₹25,000.00 per...