AGM - Drug - Corporate Regulatory Affairs – Regulatory Affairs | Venus Remedies | Dappar, Punjab, India
Venus Remedies is inviting applications for the position of AGM - Drug - Corporate Regulatory Affairs at its Dappar, Punjab operations. This full-time opportunity is ideal for experienced professionals with 10 to 15 years of expertise in pharmaceutical regulatory affairs, corporate compliance systems, international drug regulations, documentation management, and regulatory coordination activities. The selected candidate will manage regulatory submissions, oversee compliance processes, coordinate with regulatory authorities, and support strategic pharmaceutical business operations. Candidates with experience in global regulatory frameworks, audit compliance, licensing procedures, and pharmaceutical legal documentation will be preferred. This role provides leadership exposure to international regulatory systems, corporate compliance operations, and strategic pharmaceutical management activities within a professionally managed healthcare organization.
Location
Dappar, Punjab, IndiaEmployment Type
Full-timeExperience Required
10 to 15Compensation & Benefits
Competitive executive compensation package with leadership responsibilities, international regulatory exposure, and long-term career advancement opportunities.About Venus Remedies
Venus Remedies is engaged in pharmaceutical manufacturing, global healthcare operations, research-driven product development, and regulated pharmaceutical business systems.Position Overview
The AGM - Drug - Corporate Regulatory Affairs will manage corporate regulatory activities, compliance systems, and pharmaceutical regulatory coordination operations.Key Responsibilities
- Manage pharmaceutical regulatory submission activities.
- Coordinate with national and international regulatory authorities.
- Monitor compliance with pharmaceutical regulations and standards.
- Prepare and review regulatory documentation.
- Support audit readiness and compliance programs.
- Coordinate with quality assurance and legal departments.
- Monitor changes in global pharmaceutical regulations.
- Maintain regulatory records and documentation systems.
- Support strategic regulatory planning activities.
- Prepare reports related to compliance and regulatory operations.
Required Skills & Competencies
- Strong knowledge of pharmaceutical regulatory affairs.
- Understanding of international compliance systems.
- Leadership and team management capabilities.
- Excellent communication and coordination skills.
- Analytical thinking and documentation expertise.
- Awareness of audit and licensing procedures.
- Problem-solving and strategic planning abilities.
- Attention to detail and compliance accuracy.
- Time management and organizational skills.
- Capability to work in regulated pharmaceutical environments.