CORONA Remedies Regulatory Affairs Manager Jobs

CORONA Remedies Limited is hiring for a senior-level Regulatory Affairs position at its Head Office in Ahmedabad.
The company is looking for experienced professionals with strong expertise in regulatory submissions, product registrations, and compliance.
The position requires 10–15 years of experience along with a qualification in M.Pharm., B.Pharm., or M.Sc.
Interested candidates can explore the role and connect with CORONA Remedies through its official website for more details.

CORONA Remedies Limited – Regulatory Affairs Department

Regulatory Affairs Manager / Sr. Manager

Job Location: CORONA Remedies Limited – Head Office, Ahmedabad

Qualification: M.Pharm. / B.Pharm. / M.Sc.

Experience: 10–15 Years

Job Summary

Key Responsibilities

• Lead regulatory due diligence and manage global product registrations, renewals, variations, and other regulatory submissions in compliance with timelines.
• Oversee technical evaluation of dossiers, deficiency responses, labeling, and post-marketing reports to ensure accuracy and regulatory compliance.
• Develop and implement regulatory strategies supporting product development, registration, lifecycle management, and business objectives.
• Monitor regulatory changes, assess impact, and provide strategic recommendations to stakeholders and senior management.
• Collaborate with cross-functional teams to ensure timely product launches, uninterrupted supply, and market expansion.
• Liaise with health authorities, partners, affiliates, and consultants for timely exchange of regulatory information.
• Act as primary regulatory contact for authorities and manage correspondence, inspections, audits, and GMP interactions.
• Drive timely resolution of queries and compliance gaps through effective coordination and risk-based decision-making.
• Track compliance metrics, identify risks and opportunities, and present actionable insights in management reviews.
• Support regulatory intelligence and stay updated on global trends and best practices.
• Provide leadership, mentoring, and guidance to the regulatory team to ensure capability development and high standards.

Required Skills

Regulatory Affairs & Compliance

• Regulatory Strategy & Compliance Management
• Global Product Registration & Lifecycle Management
• Health Authority Interactions
• Regulatory Intelligence & Risk Assessment
• Cross-Functional Stakeholder Management
• Technical Dossier Review & Submission Management

Eligibility & Qualifications

CORONA Remedies Limited – Regulatory Affairs

M.Pharm. | B.Pharm. | M.Sc.

Experience: 10–15 Years

Candidates should have relevant senior-level experience in pharmaceutical regulatory affairs, including regulatory submissions, product registration, compliance, dossier review, and health authority interactions.

Job Location

CORONA Remedies Limited – Head Office

Mondeal Business Park, Near Gurudwara, S.G. Highway, Ahmedabad

How to Apply

Interested candidates can visit the official CORONA Remedies website for further information regarding the opportunity.

Website: www.coronaremedies.com

Job Summary

Tagged as: GMP, Qualification, Regulatory Affairs, Regulatory Compliance, Regulatory Submissions