Regulatory Affairs Cdsco Executive

We are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility of this role is to assist our clients in obtaining the necessary licenses and registrations from the Central Drugs Standard Control Organization (CDSCO) to establish and operate their pharmacy shops...

We are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility of this role is to assist our clients in obtaining the necessary licenses and registrations from the Central Drugs Standard Control Organization (CDSCO) to establish and operate their pharmacy shops...

We are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility of this role is to assist our clients in obtaining the necessary licenses and registrations from the Central Drugs Standard Control Organization (CDSCO) to establish and operate their pharmacy shops...

Role Description This is a full-time on-site role for a Regulatory Affairs Associate at OMC Medical Limited. The Regulatory Affairs Associate will be responsible for handling regulatory documentation, ensuring regulatory compliance, understanding regulatory requirements, preparing regulatory submissions, and managing overall regulatory affairs for medical...

Role Description   This is a full-time on-site role for a Regulatory Affairs Associate at OMC Medical Limited. The Regulatory Affairs Associate will be responsible for handling regulatory documentation, ensuring regulatory compliance, understanding regulatory requirements, preparing regulatory submissions, and managing overall regulatory affairs for medical...

Role DescriptionThis is a full-time on-site role for a Regulatory Affairs Associate at OMC Medical Limited. The Regulatory Affairs Associate will be responsible for handling regulatory documentation, ensuring regulatory compliance, understanding regulatory requirements, preparing regulatory submissions, and managing overall regulatory affairs for medical...

Location: IIT Madras Research park, Chennai, IndiaPosition Type: Quality Assurance & Regulatory Affairs (QA/RA) Specialist(Full Time)Salary: Based on ExperienceCompany OverviewWe, “Floaid Medtech” is an evolving venture aiming towards the development of cutting edge medical devices, motivated with “Make In India” vision. Our own vision is to provide...

Location: IIT Madras Research park, Chennai, IndiaPosition Type: Quality Assurance & Regulatory Affairs (QA/RA) Specialist(Full Time)Salary: Based on ExperienceCompany OverviewWe, “Floaid Medtech” is an evolving venture aiming towards the development of cutting edge medical devices, motivated with “Make In India” vision. Our own vision is to...

On-Call Contractor for Regulatory Affairs in Medical Device ComplianceWorkload: Approximately 40-50 hours per year, on-callKey Requirements:- Expertise in Indian Medical Device Regulations: Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly for Class C and D products.- Regulatory Experience: Proven...

We are seeking a highly skilled Regulatory Affairs Manager to join our team at Domnic Lewis International in BKC, Mumbai. This role is responsible for ensuring the highest professional standards in Regulatory Affairs and Pharmacovigilance to align with business objectives, values, and regulatory compliance.Key Responsibilities:Maintain and upload data to...

On-Call Contractor for Regulatory Affairs in Medical Device ComplianceWorkload: Approximately 40-50 hours per year , on-callKey Requirements :Expertise in Indian Medical Device Regulations : Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly for Class C and D products.Regulatory Experience : Proven...

We are looking for an Assistant Manager- Regulatory Affairs and Pharmacovigilance for a Global Pharmaceutical MNC based in BKC, MumbaiPosition: Assistant Manager- Regulatory Affairs (Domestic market)Experience: 7+ in Regulatory affairs for domestic marketLocation: BKC, MumbaiPurpose of the Role:Ensure the highest professional standards in Regulatory Affairs...

CLIENT: Leading Pharma organization servicing regulated markets like US, Europe and developing markets of Africa and Asia.Key Drivers:Manage day-to-day regulatory operations along with quality assurance, implementation & Regulatory compliance in line with (GRP) Good Regulatory practice and cGMP best practices industry / Pharmaceutical field.Maintaining the...

On-Call Contractor for Regulatory Affairs in Medical Device ComplianceWorkload: Approximately 40-50 hours per year, on-callKey Requirements:Expertise in Indian Medical Device Regulations: Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly for Class C and D products.Regulatory Experience: Proven experience...

On-Call Contractor for Regulatory Affairs in Medical Device Compliance Workload: Approximately 40-50 hours per year , on-call Key Requirements : Expertise in Indian Medical Device Regulations : Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly for Class C and D products . Regulatory Experience : Proven...

On-Call Contractor for Regulatory Affairs in Medical Device ComplianceWorkload: Approximately 40-50 hours per year, on-callKey Requirements:Expertise in Indian Medical Device Regulations: Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly for Class C and D products.Regulatory Experience: Proven experience...

Transform Patient Care with AI-Powered SolutionsWe are seeking an experienced Regulatory Affairs Specialist to join our team at Dozee, a leading provider of AI-based contactless Remote Patient Monitoring (RPM) and Early Warning System (EWS).About the Role:In this pivotal position, you will play a crucial role in ensuring compliance with regulatory...

Company OverviewDomnic Lewis International is a global pharmaceutical company seeking an experienced Regulatory Affairs Manager to join its team in Mumbai.Job DescriptionWe are looking for a highly skilled and dedicated individual to lead our regulatory affairs efforts in the domestic market. The successful candidate will be responsible for ensuring...

On-Call Contractor for Regulatory Affairs in Medical Device ComplianceWorkload: Approximately 40-50 hours per year , on-callKey Requirements :Expertise in Indian Medical Device Regulations : Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly for Class C and D products .Regulatory Experience : Proven...

On-Call ContractorforRegulatory Affairs in Medical Device ComplianceWorkload:Approximately40-50 hoursper year , on-callKey Requirements :Expertise in Indian Medical Device Regulations : Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly forClass C and D products .Regulatory Experience : Proven experience in...