Regulatory Affairs Officer

• Review regulatory guidelines for registration of Pharmaceutical Drug and/or Medical Device for the market
• Prepare documents as per guidelines.
• Review documents thoroughly
• Rectify documentation queries from regulatory bodies
• Manage samples for submission
• Manage/Review artwork for submission
• Coordinate with other team members to ensure swift workflow
• Prompt response, attention to detail, good communication skills
• Ability to work at fast pace
• Other duties as assigned
• Experience in using MS OFFICE, ADOBE ACROBAT, COMPUTER SKILLS required

Job Types: Full-time, Permanent

Pay: ₹20,000.00 - ₹30,000.00 per month

Benefits:

• Flexible schedule
• Paid time off

Education:

• Diploma (Required)

Experience:

• Pharmaceutical QA/QC documentation: 2 years (Required)

Work Location: In person