Current jobs related to Medical Device Regulatory Coordinator - Ahmedabad, Gujarat - Medical Device Manufacturing

  • Medical Device Regulatory Affairs Professional

    7 days ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    Role Summary:The Regulatory Affairs Associate will be responsible for ensuring compliance with international regulatory guidelines and overseeing the preparation and submission of regulatory dossiers for pharmaceutical products in Rest of the World (ROW), Asian, and African markets.Main Responsibilities:Preparation and submission of regulatory dossiers,...

  • International Regulatory Coordinator

    6 days ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    Job Title: International Regulatory Affairs ExecutiveCompany Overview:We are a leading medical device manufacturing company with a global presence. Our products cater to various healthcare needs, including urology, laparoscopy, gynecology, dialysis, cardiology, and gastrology.Job Summary:The successful candidate will be responsible for preparing and...

  • Medical Device Compliance Officer

    7 days ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    We are seeking a highly motivated Medical Device Compliance Officer to join our team in ensuring compliance with international regulatory guidelines and facilitating product approvals.Key Responsibilities:Prepare and review technical documents, including stability data, product formulation, and analytical reports.Liaise with internal departments such as R&D,...

  • Regulatory Affairs Specialist

    7 days ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    Our client, a leading medical device manufacturer, is seeking an experienced Regulatory Affairs Specialist to join their team.Job Overview:The successful candidate will be responsible for ensuring compliance with international regulatory guidelines and coordinating with internal teams to facilitate product approvals.This role requires strong communication...

  • Global Regulatory Associate

    6 days ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    Regulatory Affairs PositionWe are a leading medical device manufacturing company seeking an experienced Regulatory Affairs professional to join our team as an International Regulatory Affairs Executive.Job Responsibilities:The successful candidate will be responsible for preparing and submitting regulatory dossiers for pharmaceutical products in Rest of the...

  • Regulatory Affairs Specialist

    6 days ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    Company OverviewOur client is a leading medical device manufacturer with a global presence, producing urology, laparoscopy, gynecology, dialysis, cardiology, and gastrology products.Their brand is recognized in over 85 countries worldwide.Job DescriptionThe International Regulatory Affairs Executive will be responsible for preparing and submitting regulatory...

  • Medical Device Compliance Expert

    6 days ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    Regulatory Affairs RoleWe are seeking an experienced Regulatory Affairs professional to join our team as an International Regulatory Affairs Executive.Job Responsibilities:The successful candidate will be responsible for preparing and submitting regulatory dossiers for pharmaceutical products in Rest of the World (ROW), Asian, and African markets.This role...

  • Regulatory Affairs Associate

    1 week ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    Company Details :Our client is an India's Largest and Leading Manufacturer and Exporter of Urology, Laparoscopy, Gynecology, Dialysis, Cardiology, and gastrology products.Their Brand Presents in More Than 85 Countries.Designation : - International RA ExecutiveJob Profile : -The International Regulatory Affairs Executive will be responsible for preparing...

  • Regulatory affairs associate

    7 days ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    Company Details : Our client is an India's Largest and Leading Manufacturer and Exporter of Urology, Laparoscopy, Gynecology, Dialysis, Cardiology, and gastrology products. Their Brand Presents in More Than 85 Countries.Designation : - International RA ExecutiveJob Profile : -The International Regulatory Affairs Executive will be responsible...

  • Regulatory Affairs Associate

    2 weeks ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    Company Details : Our client is an India's Largest and Leading Manufacturer and Exporter of Urology, Laparoscopy, Gynecology, Dialysis, Cardiology, and gastrology products. Their Brand Presents in More Than 85 Countries. Designation : - International RA Executive Job Profile : - The International Regulatory Affairs Executive will be responsible for...

  • Regulatory Affairs Associate

    2 weeks ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    Company Details: Our client is an India's Largest and Leading Manufacturer and Exporter of Urology, Laparoscopy, Gynecology, Dialysis, Cardiology, and gastrology products. Their Brand Presents in More Than 85 Countries.Designation: - International RA Executive Job Profile: -The International Regulatory Affairs Executive will be responsible for preparing and...

  • Regulatory Affairs Associate

    2 weeks ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    International Regulatory Affairs Executive The International Regulatory Affairs Executive will be responsible for preparing and submitting regulatory dossiers for pharmaceutical products in Rest of the World (ROW), Asian, and African markets. Key Responsibilities: Dossier Preparation & Submission: Ensure timely preparation and submission of dossiers,...

  • Global RA Coordinator

    7 days ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    We are looking for a skilled Global RA Coordinator to join our team in supporting the preparation and submission of regulatory dossiers for pharmaceutical products in Rest of the World (ROW), Asian, and African markets.Responsibilities:Monitor and update changes in regulatory guidelines for ROW, Asian, and African markets.Implement necessary updates in...

  • International Regulatory Executive

    7 days ago

    Ahmedabad, Gujarat, India Medical Device Manufacturing Full time

    We are looking for an International Regulatory Executive to join our team in supporting the preparation and submission of regulatory dossiers for pharmaceutical products in Rest of the World (ROW), Asian, and African markets.Responsibilities:Compile, review, and submit regulatory dossiers as per country-specific requirements.Maintain up-to-date knowledge of...

  • Medical Device Quality Manager

    7 days ago

    Ahmedabad, Gujarat, India Biotech Healthcare Full time

    Job OverviewAbout Us:Biotech Healthcare is seeking an experienced Quality Assurance professional to join our team as a Medical Device Quality Manager. The successful candidate will be responsible for leading the development and implementation of a Quality Management System (QMS) that meets regulatory requirements and industry...

  • System Architect for Medical Devices

    5 days ago

    Ahmedabad, Gujarat, India Capgemini Engineering Full time

    What You'll DoJob Summary:We're looking for a highly skilled System Architect for Medical Devices to join our team at Capgemini Engineering. As a key member of our organization, you will be responsible for developing and executing system architecture designs, defining system interfaces, and developing verification strategies.Key Responsibilities:Develop and...

  • Senior Regulatory Affairs Officer

    3 weeks ago

    Ahmedabad, Gujarat, India Lifelancer Full time

    Job Title: Senior Regulatory Affairs Officer Job Location: Ahmedabad, Gujarat, India Job Location Type: On-site Job Contract Type: Full-time Job Seniority Level: Associate Skills:Regulatory Affairs, Quality Assurance, Regulatory Strategy Development, Class III Medical Devices, Product Registration, international legislation, accreditation requirements,...

  • Senior Medical Device Sales Professional

    6 days ago

    Ahmedabad, Gujarat, India Meril Full time

    About the RoleWe are seeking a highly skilled and experienced Area Sales Manager to join our team in Ahmedabad. The ideal candidate will have a strong background in medical devices sales, with a focus on ENT division.Key ResponsibilitiesSupport the learning and development of the sales team by providing coaching and mentoringCoordinate with sales...

  • Manager - Production (Medical Device Manufacturing)

    2 weeks ago

    Ahmedabad, Gujarat, India Biotech Healthcare Full time

    Role Objective: Manager of Manufacturing is responsible for leading and overseeing the production operations which includes manufacturing and packing within the IOL device manufacturing facility. This role ensures the efficient, safe, and compliant production of pharmaceutical products while meeting quality standards and production targets. The Manager will...

  • Medical Specialist

    2 days ago

    Ahmedabad, Gujarat, India Veeda Lifesciences Full time

    Role: Medical Monitor Experience: 0 to 1 Year Location: Ahmedabad Qualification- MBBS Salary Range: 7 to 8.5 LPA Role & Responsibilities. Conduct study feasibilities (preliminary and detailed) for the clinical trials as per the proposal from Medical writing team and sponsor and preparation of feasibility questionnaire (Questionnaire related to Study patient...

Medical Device Regulatory Coordinator

1 week ago

Ahmedabad, Gujarat, India Medical Device Manufacturing Full time
About the Role

The International Regulatory Affairs Executive will play a critical role in ensuring compliance with international regulatory guidelines, coordinating with internal teams, and liaising with regulatory authorities for approvals. Key responsibilities include dossier preparation & submission, regulatory compliance & documentation, coordination & communication, and regulatory intelligence & updates.