Regulatory Affairs Associate

Roles and ResponsibilitiesPrepare dossiers, variations, renewals, and amendments for USFDA regulatory submissions.Coordinate with third-party agencies for audits and inspections (USFDA, WHO).Ensure compliance with GMP requirements through self-inspection and third-party audits.Maintain liaison with government authorities for licensing and approvals.Provide...

Job Position: Cosmetics Regulatory Affairs SpecialistWorking Days: Monday to FridayShift Time- 12 PM IST- 9 PM ISTLocation- Sector- 63, Noida We are looking for a detail-oriented and knowledgeable Cosmetics Regulatory Affairs Specialist to join our team. The ideal candidate will have a strong understanding of regulatory policies, documentation, and...

Job Position: Cosmetics Regulatory Affairs SpecialistWorking Days: Monday to FridayShift Time- 12 PM IST- 9 PM ISTLocation- Sector- 63, Noida We are looking for a detail-oriented and knowledgeable Cosmetics Regulatory Affairs Specialist to join our team. The ideal candidate will have a strong understanding of regulatory policies, documentation, and...

Company DescriptionTrishul Biotech is dedicated to advancing scientific research to enhance agricultural sustainability and productivity. Utilizing cutting-edge crop solutions, the company aims to improve agricultural quality with its unique Upcrop Research, Development, and Commercialization platform. This innovation has led to the production of impactful...

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...

Job Title:Regulatory Affairs SpecialistLocation:Okhla Phase-1, Delhi-110020Department:Regulatory AffairsReports To:Head of Quality & RegulatoryEmployment Type:Full-TimeJob Summary:We are seeking a detail-oriented and knowledgeableRegulatory Affairs Specialistto ensure our medical devices comply with all regulatory requirements in domestic and international...

**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...

Dr. Reddy's Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines becauseGood Health Can't Wait.We started in 1984 with a modest investment, 20 employees and a bold...

Gentell is one of the largest vertically integrated wound care companies in the world. Based in Yardley, PA and with offices, distribution centers and manufacturing plants around the world, our purpose is to make a positive difference in the quality of life for the injured, the chronically ill and those near the end of life. Our success is a result of the...