Job Description

Develop and implement regulatory strategies to ensure compliance with local and international regulations. Oversee the preparation and submission of regulatory documents, including Drug Master Files (DMFs), ANDAs, and other submissions. Provide regulatory guidance and support to cross-functional teams throughout the product development lifecycle. Liaise with regulatory agencies and manage communications regarding product registrations, approvals, and compliance. Stay updated on evolving regulatory guidelines, industry trends, and best practices to drive continuous improvement initiatives. Lead regulatory inspections and audits, ensuring readiness and facilitating successful outcomes. Collaborate with internal stakeholders (QA/QC/R&D, and other support functions) and external partners to resolve regulatory issues and address inquiries promptly.
Job Type: Full-time

Pay: ₹60,000.00 - ₹80,000.00 per month

Benefits:

Cell phone reimbursement Flexible schedule Food provided Leave encashment Paid sick time Provident Fund
Experience:

total work: 1 year (Preferred)
Work Location: In person