Looking for Regulatory Affairs Trainer. We can provide 6k per batch and remote and only 1.5 to 2 hours per day after 6pm
Job Summary:
We are seeking a knowledgeable and experienced Regulatory Affairs Trainer to design and deliver high-quality training programs for professionals and students aspiring to enter the pharmaceutical and healthcare regulatory sector. The trainer will be responsible for developing curriculum, conducting live sessions (online/offline), preparing course materials, and keeping trainees updated on global regulatory standards and trends.
Key Responsibilities:
- Develop and deliver training modules on global regulatory affairs (USFDA, EMA, CDSCO, MHRA, TGA, etc.).
- Explain key regulations, guidelines, and submission processes for pharmaceuticals, biologics, and medical devices.
- Train candidates on CTD/eCTD formats, regulatory submissions, labeling, and compliance.
- Provide hands-on training on documentation, dossier preparation, and regulatory software/tools.
- Update training content as per the latest international regulatory requirements.
- Assess trainee progress through assignments, quizzes, and mock interviews.
- Guide students on career opportunities and certification exams in regulatory affairs.
- Collaborate with the academic and operations team for scheduling and feedback collection.
Required Skills & Qualifications:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or a related field.
- Minimum 3–5 years of hands-on experience in Regulatory Affairs.
- In-depth knowledge of ICH guidelines, IND/NDA/ANDA submissions, and post-marketing requirements.
- Experience in teaching/training or a passion for mentoring is preferred.
- Strong communication and presentation skills.
- Ability to explain complex concepts in a simple and engaging manner.
Job Type: Part-time
Pay: ₹6,000.00 per month
Expected hours: 10 per week
Benefits:
- Work from home
Schedule:
- Evening shift
Experience:
- regulatory affairs: 2 years (Preferred)
Work Location: Remote