ProPharma | Regulatory Affairs Specialist

We are seeking a highly skilled Regulatory Affairs Associate or Junior Regulatory Affairs Manager with proven expertise in Veeva Vault to join our team on a 6-month contractual basis with the potential for extension. The ideal candidate will support regulatory data reconciliation and content management efforts, ensuring accurate and streamlined...

ProPharma is seeking a skilled Regulatory Affairs Associate or Junior Regulatory Affairs Manager with expertise in Veeva Vault to support regulatory data reconciliation and content management efforts on a 6-month contractual basis with potential for extension.About the RoleThis position involves working closely with regulatory product teams to streamline...

We are seeking a highly skilled Regulatory Affairs Associate or Junior Regulatory Affairs Manager with proven expertise in Veeva Vault to join our team on a 6-month contractual basis with the potential for extension. The ideal candidate will support regulatory data reconciliation and content management efforts, ensuring accurate and streamlined...

Company OverviewOMC Medical Limited is a leading healthcare company based in the UK, specializing in regulatory services for medical devices. We offer comprehensive solutions to the healthcare industry.Job DescriptionThis is a full-time, remote-based role for a Regulatory Affairs Human Resources Specialist at OMC Medical Limited. The successful candidate...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to lead our Regulatory Publishing team. The ideal candidate will have 6+ years of experience in eCTD Regulatory Publishing and strong knowledge of eCTD process.Key Responsibilities:Liaise with cross-functional teams to ensure compliance with government acts and regulations.Oversee...

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...

FICCI, a prominent industry chamber, seeks an experienced Regulatory Affairs Specialist to join their team. This individual will play a crucial role in supporting the organization's work related to the medical devices and equipment sector.The ideal candidate will have a strong understanding of policies and regulations in the medical devices sector, as well...

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...

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...

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...

About Qure.AI:Qure.AI is the world's fastest-growing medical AI company, boasting an impressive 18 FDA and 62 CE marking clearances to date. We develop cutting-edge solutions that significantly enhance patient outcomes across various care domains, including lung cancer, tuberculosis, and stroke. Our innovative technologies have positively impacted over 22...

About Qure.AI:Qure.AIis the world's fastest-growing medical AI company, boasting an impressive 18 FDA and 62 CE marking clearances to date. We develop cutting-edge solutions that significantly enhance patient outcomes across various care domains, including lung cancer, tuberculosis, and stroke. Our innovative technologies have positively impacted over 22...

About Zuari Management Services Limited: We are a leading provider of financial services, offering a wide range of products and solutions to meet the evolving needs of our customers. Our commitment to excellence drives us to deliver high-quality services.Job Title: Compliance OfficerThis role requires an individual with expertise in regulatory affairs,...

Designation: - **Drug Regulatory Affairs-Male/Female** **JOB DESCRIPTION: -** - Delivery/Proper packing of goods for supplier - Maintaining the stock status at the back office - Settling of credit notes and following ups of payments from the parties - Coordinate with the vendors by keeping the track on purchase & delivery of orders sent - Maintaining the...

DESIGNATION/ TITLE Sr. Executive / Assistant Manager - Regulatory Affairs LOCATION NSP, Delhi YEAR OF EXP Minimum 3 yrs QUALIFICATION MSc (Toxicology/Agri/Chem) or similar BUDGET In b/w 8-10Lpa KEY RESPONSIBILITIES ROLES & RESPONSIBILITIES Manage the data gathering and compilation of studies (toxicology, chemical, efficacy) necessary for the...

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...