Regulatory Affairs Executive

Uniza Healthcare is hiring professionals for the role of Regulatory Affairs Executive for its pharmaceutical regulatory operations in Ahmedabad, Gujarat, India. This full-time opportunity is suitable for candidates with 0 to 2 years of experience in regulatory affairs, pharmaceutical documentation, dossier preparation, compliance management, product registration activities, regulatory submissions, healthcare regulations, documentation control systems, quality compliance, and pharmaceutical regulatory processes.

The selected candidate will support regulatory affairs activities related to pharmaceutical business operations. Responsibilities include preparing and maintaining regulatory documentation, supporting dossier compilation and submission activities, ensuring compliance with pharmaceutical regulations and quality standards, coordinating with quality assurance and production teams, maintaining regulatory records and documentation systems, monitoring compliance requirements and submission timelines, participating in regulatory review meetings and coordination discussions, assisting in issue resolution and corrective action implementation, supporting workflow management and reporting systems, and contributing to continuous improvement initiatives related to regulatory compliance operations. Candidates should possess strong understanding of pharmaceutical regulatory workflows and documentation systems.

This opportunity provides valuable exposure to pharmaceutical regulatory systems, compliance management workflows, documentation control activities, product registration processes, regulatory reporting systems, and modern pharmaceutical environments within a reputed healthcare organization. Professionals interested in regulatory affairs and pharmaceutical compliance can strengthen their technical and operational expertise through this opportunity.

Location

Ahmedabad, Gujarat, India

Employment Type

Full-time

Experience Required

0 to 2

About Uniza Healthcare

Uniza Healthcare operates in the pharmaceutical industry specializing in healthcare product systems, pharmaceutical compliance operations, regulatory documentation activities, and quality-focused business solutions.

Key Responsibilities

• Prepare and maintain regulatory documentation.
• Support dossier compilation and submission activities.
• Ensure compliance with regulatory requirements.
• Coordinate with quality and production teams.
• Maintain regulatory records and reporting systems.
• Monitor compliance requirements and timelines.
• Participate in regulatory review meetings.
• Assist in issue resolution and corrective actions.
• Support workflow management and reporting.
• Contribute to continuous improvement initiatives.

Required Skills

• Knowledge of pharmaceutical regulatory affairs.
• Understanding of compliance and documentation systems.
• Awareness of dossier preparation processes.
• Communication and coordination skills.
• Problem-solving and analytical abilities.
• Documentation management expertise.
• Time management and planning skills.
• Attention to detail and compliance.
• Teamwork and collaboration abilities.
• Adaptability to pharmaceutical environments.

Educational Qualification

B.Pharm

Industry

Pharmaceutical

Why Join Uniza Healthcare?

Uniza Healthcare offers professionals opportunities to work in modern pharmaceutical environments with exposure to regulatory systems and compliance management practices.