Executive- International Affairs

**Job Title: Medical Device Regulatory Affairs Intern** **Overview** As a Medical Device Regulatory Affairs Intern, you will support managing the regulatory processes for medical devices. You will assist in preparing documentation, conducting research, and ensuring compliance with regulatory requirements. This internship provides a valuable opportunity to...

Company Description GESCO Healthcare is a leading manufacturer and exporter of spinal, orthopaedic, and CMF implants and surgical instruments in the Asia-Pacific region. With over 60 years of experience, GESCO has transformed the lives of over 120 million people. The company's innovation center leads the way in developing path-breaking and cost-effective...

We are in the process of hiring Regulatory Affairs **Job Title**: Regulatory Affairs Executive **Key Responsibilities**: **Qualifications**: Bachelor Degree in a related field such as Biomedical engineering, Mechanical engineering with minimum of 5 to 7 years’ progressive Regulatory affairs experience in medical device & quality...

Full job description **Key Responsibilities**: - Monitor and stay up-to-date on regulatory changes and requirements in different regions. - Communicate with regulatory authorities and answer their queries or requests. - Ensure product labeling and packaging meet regulatory standards. - Maintain records of regulatory submissions, approvals, and...

Experience: 0 to 1 years of experience in Regulatory affairs. Qualification: B. Pharm / M. Pharm / MSc. Biotechnology Description: Regulatory Affairs Handling Dossiers License Queries CFT Communication Life cycle etc. *Immediate Joiners* Excellent in Communication Application Question(s): - Current CTC - Expected CTC - Notice...

**Key Responsibilities** - **Fee Collection and Management**: - Handle fee collection from students, including tuition fees, examination fees, and other payments. - Issue receipts for payments made and maintain accurate records of all transactions. - Ensure timely follow-up on outstanding dues and communicate reminders to students or parents. - Reconcile...

We're Hiring – Senior Engineer (Regulatory Affairs | QARA Department) Location: Coimbatore Company: Iatome Electric India Pvt. Ltd.Are you passionate about quality, compliance, and regulatory excellence in the medical device industry?We're looking for an experienced professional to join our QARA (Quality & Regulatory Affairs) team Position: Sr. Engineer...

**Key Responsibilities**: - **Regulatory Compliance**: Ensure compliance with ISO 13485, EU MDR 2017/745, US-FDA, CDSCO, and other applicable international standards for medical devices. - **Submissions and Approvals**: Prepare, review, and submit regulatory documentation, including 510(k) and IMDR submissions, to regulatory authorities such as US-FDA,...

Job Summary: We are looking for Manager - Government Affairs & Capital Planning, will be responsible for ensuring regulatory compliance, securing government approvals and incentives, and supporting capital project execution for Johnson Electric’s expanding operations in India. This role will play a critical part in the successful setup and consolidation of...

Job Summary:We are looking for Manager - Government Affairs & Capital Planning, will be responsible for ensuring regulatory compliance, securing government approvals and incentives, and supporting capital project execution for Johnson Electric’s expanding operations in India. This role will play a critical part in the successful setup and consolidation of...