Join a leading global medical technology company and play a vital role in ensuring post-market safety, managing product complaints, and maintaining regulatory compliance under Good Vigilance Practice (GVP) and the PMD Act. As an Associate GVP Safety Manager, you will lead safety operations, oversee compliance reporting, and develop a high-performing team to uphold the highest safety and quality standards for medical devices and therapies used worldwide.
Key Responsibilities
- Collect, analyze, and manage post-market safety data to ensure patient safety.
- Oversee product complaints and ensure proper investigation, documentation, and resolution.
- Maintain regulatory compliance and handle pharmacovigilance reporting under GVP.
- Implement risk management and safety monitoring procedures.
- Lead and develop a team to drive efficient safety operations and continuous improvement.
Required Skills and Qualifications
- Experience:
- Minimum 3 years of experience in complaint handling and GVP-related activities within the medical industry.
- Proven team management and leadership experience.
- Language Requirements:
- Japanese: Native level (essential for regulatory compliance and reporting).
- English: Business level (for global collaboration and documentation).
Preferred Skills & Qualifications
- Experience as a Safety Management Supervisor in a regulated industry.
- Strong background in project management and cross-functional collaboration.
- Knowledge and experience in risk management and compliance procedures.
About the Company
Our client is a global leader in medical technology, specializing in the development, manufacturing, and distribution of cutting-edge medical devices, diagnostics, and biosciences solutions. Their products are widely used across healthcare institutions, clinical laboratories, pharmaceutical companies, and life science research organizations, with a strong focus on medication delivery, diagnostics, and advancing medical discovery.
Why You'll Love Working Here
- Impact on Patient Safety: Contribute directly to enhancing global healthcare safety and patient outcomes.
- Global Regulatory Exposure: Gain valuable experience working with international pharmacovigilance regulations and compliance frameworks.
- Career Growth & Development: Expand expertise in safety management, team leadership, and global compliance.
- Work-Life Balance: Enjoy a five-day workweek, paid holidays, and flexible work arrangements.
- Comprehensive Benefits: Social insurance, transportation allowance, childcare leave, and special leave options.
Don't Miss Out - Apply Now!
