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 operations...

We are seeking a highly skilled Regulatory Affairs Specialist to join our team at ProPharma 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 operations within Veeva Vault.Key ResponsibilitiesData Reconciliation and...

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...

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 operations...

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners...

The Hird is seeking a highly skilled Senior Regulatory Affairs Specialist to join our team in a remote location. This role offers a competitive salary of up to 19 LPA, with an estimated average annual compensation of 18.5 LPA.About the Role:We are looking for a seasoned professional with extensive experience in regulatory affairs and medical writing. As a...

Job Title: Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team in Bengaluru. As a key member of our organization, you will play a vital role in ensuring compliance with regulatory requirements and driving the success of our medical device testing business.About Us:BioTalent Search Private Limited is a...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Biocon in US/Canada Market. This role is an exciting opportunity for individuals with experience in formulation regulatory affairs.Key ResponsibilitiesPrepare, review and submit ANDA/ANDS in the US Market, including modules.Contribute to life cycle management for...

Apsida Life Science seeks an experienced Senior Regulatory Affairs Specialist to collaborate with our Global Regulatory Team Leads and submission teams. As a key member of our regulatory team, you will be responsible for ensuring timely and high-quality submissions that comply with global guidelines and company SOPs.The ideal candidate will have in-depth...

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...

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...

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...

Job Overview:We are seeking a seasoned Pharma Regulatory Affairs expert to join our team at Profile HR Consultants Pvt Ltd.About the Role:Manage regulatory operations, quality assurance, implementation and compliance in line with GRP and cGMP best practices.Maintain regulatory and QMS documentation as per cGRP and cGMP regulations.Coordinate between Company...

The Regulatory Manager will be responsible for overseeing and ensuring that all food compliance mandates related to FSSAI and AYUSH formulation guidelines are strictly adhered to. This includes managing compliance for Zeon's domestic product range, which covers Proprietary Foods, Nutraceuticals, Health Supplements, Food for Special Dietary Users (FSDU),...

Location: IIT Madras Research park, Chennai, India Position Type: Quality Assurance & Regulatory Affairs (QA/RA) Specialist(Full Time) Salary: Based on Experience Company Overview We, “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...

About the RoleThis is a full-time on-site position for a Regulatory Affairs Associate at OMC Medical Limited. The successful candidate will be responsible for handling regulatory documentation, ensuring regulatory compliance with medical devices and cosmetics regulations, and managing overall regulatory affairs.Key ResponsibilitiesPreparing and reviewing...

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...

**Job Description**: You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping...

Job Description:We are seeking an experienced Regulatory Affairs Manager to join our team at Intas Pharmaceuticals. This role will be responsible for preparing and submitting applications and dossiers for registration of recombinant products, CGT products in India, and PCT applications.The successful candidate will have a strong background in pharmaceutical...