Job Opportunity: Regulatory Affairs Manager
We are looking for a dynamic and self-driven Regulatory Affairs Manager to spearhead our documentation and compliance department. We need a proactive professional with a sharp eye for detail who can take full ownership of our international dossier pipeline and drive high-stakes projects to completion.
Key Responsibilities
- Dossier Mastery: Lead the end-to-end preparation, compilation, and technical checking of ASEAN Common Technical Dossiers (ACTD).
- Export Compliance: Oversee and verify HOTC export dossiers to ensure seamless international submissions and approvals.
- Quality Leadership: Act as the final authority on technical accuracy, ensuring all documentation is 100% compliant with global Ministry of Health standards.
- Strategic Workflow: Manage timelines with high energy, ensuring that registration goals for international markets are met efficiently.
Required Qualifications
- Experience: Minimum of 5 years of proven experience in Pharmaceutical Regulatory Affairs.
- Technical Expertise: Specialized knowledge in ACTD formats and international export documentation.
- Education: B.Pharm, Pharm.D, or a relevant Master’s degree.
- Core Attributes: We are seeking a young and energetic individual who is career-oriented and capable of working with minimal supervision.
Compensation & Benefits
- Salary: Market-competitive salary package based on experience and technical expertise.
- Growth: Opportunities for professional development in a growing international business environment.
Job Details
- Location: Karachi (Office conveniently located near the Karachi Chamber of Commerce and Industry).
- Gender: Open to both Male and Female candidates.
- Type: Full-time.
Experience:
- regulatory manager: 4 years (Required)
Work Location: In person