Senior Executive - Regulatory Affairs

Acme Generics is hiring professionals for the role of Senior Executive Regulatory Affairs for its pharmaceutical regulatory operations in Ahmedabad, Gujarat, India. This full-time opportunity is suitable for candidates with 3 to 10 years of experience in regulatory affairs, dossier preparation, product registration, compliance management, documentation control, submission activities, regulatory strategy, pharmaceutical regulations, audit support, and healthcare product compliance systems.

The selected candidate will support regulatory affairs activities related to pharmaceutical business operations. Responsibilities include preparing and reviewing regulatory dossiers, maintaining regulatory documentation and compliance records, supporting product registration and submission activities, ensuring adherence to regulatory guidelines and pharmaceutical standards, coordinating with quality assurance and production teams, monitoring compliance requirements and regulatory timelines, participating in regulatory review meetings and technical discussions, assisting in issue resolution and corrective action implementation, supporting audit readiness activities, and contributing to continuous improvement initiatives related to regulatory compliance and documentation systems.

This opportunity provides valuable exposure to pharmaceutical regulatory systems, compliance management workflows, product registration activities, documentation control operations, submission management systems, and modern pharmaceutical business environments.

Location

Ahmedabad, Gujarat, India

Employment Type

Full-time

Experience Required

3 to 10

About Acme Generics

Acme Generics operates in the pharmaceutical industry specializing in healthcare product systems, pharmaceutical manufacturing operations, regulatory compliance activities, and quality-focused business solutions.

Educational Qualification

B.Pharm

Industry

Pharmaceutical

Why Join Acme Generics?

Acme Generics offers professionals opportunities to work in compliance-focused pharmaceutical environments with exposure to advanced regulatory systems and healthcare product operations.