Regulatory Affairs Trainer

2 days ago


Noida Uttar Pradesh, India Technoledge Eduresearch Pvt Ltd Full time

**Company Description**

Technoledge is an educational institution located in Noida. Our primary objective is to provide support for the development, coordination, implementation, and planning of educational programs. We offer a wide range of services including smart hybrid schools, engineering services, manpower solutions, skill development, e-learning processes, and study abroad programs. Our goal is to maximize efficiency and provide a shared learning experience that leads to improved performance and empowerment.

**Role Description**

This is a full-time on-site role for a Regulatory Affairs Trainer. The Regulatory Affairs Trainer will be responsible for conducting training sessions on regulatory affairs and ensuring compliance with relevant regulations. They will develop training materials, deliver presentations, and provide guidance on regulatory requirements. The Regulatory Affairs Trainer will also collaborate with cross-functional teams to develop and implement training programs.

**Qualifications**
- Knowledge of regulatory affairs and compliance
- Experience in conducting training sessions and developing training materials
- Excellent presentation and communication skills
- Ability to collaborate with cross-functional teams
- Attention to detail and strong analytical skills
- Experience in the education industry is a plus
- Bachelor's degree in a relevant field

**Job Types**: Full-time, Freelance
Contract length: 2 months

**Salary**: ₹25,000.00 - ₹30,000.00 per month

Schedule:

- Monday to Friday

**Experience**:

- total work: 2 years (required)

Work Location: In person



  • Noida, Uttar Pradesh, India Bhargava HR solution Full time

    This is a full-time on-site role as a Junior Regulatory Affairs Executive located in Noida. The Junior Regulatory Affairs Executive will be responsible for regulatory documentation, ensuring compliance with regulatory requirements, preparing dossiers, and managing regulatory affairs. **Qualifications**: Regulatory Documentation, Regulatory Requirements, and...


  • Noida, Uttar Pradesh, India BHARGAVA HR SOLUTION Full time

    **Role Description** This is a full-time on-site role as a Junior Regulatory Affairs Executive located in Noida. The Junior Regulatory Affairs Executive will be responsible for regulatory documentation, ensuring compliance with regulatory requirements, preparing dossiers, and managing regulatory affairs. **Qualifications** - Regulatory Documentation,...


  • Noida, Uttar Pradesh, India Florencia Healthcare Full time

    **JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

  • Regulatory Affairs

    6 days ago


    Andhra Pradesh, India Virtusa Full time

    Regulatory Affairs Specialist Careers that Change Lives Collaborate and partner with Design QA, R&D, Sustaining Engineering, Clinical Affairs, Marketing and Operations. Supports the Global Operating Unit Regulatory Affairs function as the local representative for ensuring requirements are met. Responsible for supporting the needs of the MEIC with regulatory...


  • Noida, India Florencia Healthcare Full time

    Regulatory affairs professionals play a critical role in the drug development process, working closely with other stakeholders to ensure that pharmaceutical products meet regulatory requirements at every stage of development. Some of their key responsibilities include ( CTD/ ACTD DOSSIER PREPRATION ( MARKET ASEAN, CIS ROW ) **Regulatory Strategy...


  • Noida, India Florencia Healthcare Full time

    Regulatory affairs professionals play a critical role in the drug development process, working closely with other stakeholders to ensure that pharmaceutical products meet regulatory requirements at every stage of development. Some of their key responsibilities include ( CTD/ ACTD DOSSIER PREPRATION ( MARKET ASEAN, CIS ROW ) **Regulatory Strategy...


  • Noida, Uttar Pradesh, India diligence certifications Full time

    **Key Responsibilities**: - Understand regulatory services offered by the company (BIS, CDSCO, etc.) - Identify and approach potential clients in pharmaceutical, biotech, and related industries - Build and maintain strong client relationships to ensure repeat business - Provide accurate information to clients regarding regulatory approvals and...


  • Noida, Uttar Pradesh, India MyOperator Full time

    Are you an experienced and results-oriented professional with a profound understanding of **Indian telecom regulations** and a knack for strategic engagement with government authorities? We're seeking a **Manager / Senior Manager - Regulatory Affairs** to lead our efforts in navigating the complex regulatory landscape, ensuring full compliance, and...


  • Noida, India Docthub Health Tech Private Limited Full time

    **Description** Drug Regulatory Affairs - Job description - Prepare CTD, ACTD Dossiers and file regulatory submissions. - Perform assessments of new or revised products. - Manage complaint documentation (including investigation and closure). - Respond to inquiries from regulatory bodies. - Should be technically well versed with requirements for medicines...


  • Noida, Uttar Pradesh, India Devine Meditech Full time US$ 80,000 - US$ 1,20,000 per year

    Job Title:Regulatory Affairs SpecialistLocation:Okhla Phase-1, Delhi-110020Department:Regulatory AffairsReports To:Head of Quality & RegulatoryEmployment Type:Full-TimeJob Summary:We are seeking a detail-oriented and knowledgeableRegulatory Affairs Specialistto ensure our medical devices comply with all regulatory requirements in domestic and international...