Associate - Regulatory Operations
5 months ago
**Your Key Responsibilities**:
Your responsibilities include, but not limited to:
- To ensure the smooth running of the Drug Regulatory Affairs Department through providing professional secretarial service & assistance, and to contribute to the achievement of functional objectives.
- Learns to use basic principals, theories, and professional concepts.
- Applies company policies & procedures to resolve routine issues.
- Contacts are primarily with immediate supervisor and other personnel in department or group -Works on problems of routine scope.
- Follows established policies and procedures.
- Normally receives detailed instructions on all work -Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt -Distribution of marketing samples (where applicable)
**What you’ll bring to the role**:
**Essential Requirements**:
- 3+ years of experience on Regulatory experience
- Cross Cultural Experience.
- Operations Management and Execution.
- Collaborating across boundaries.
**Why Sandoz?**:
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more
With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
The future is ours to shape
**Commitment to Diversity & Inclusion (hard coded in Brassring)**:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
**#Sandoz**
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