- Full Time
- Intern
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Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
Job description
Key Responsibilities:
1.1 Managing and coordinating regulatory processes
- This includes registration, as well as preparing and maintaining regulatory documentation.
- Gather, file, and maintain all data/ information regarding FSCA/ AE/ Customer Complaint and any other related QA/RA issues.
1.2 Collaborating with RAQA project teams
- Support any Quality Regulatory Compliance related special projects that assigned by company policy as well as Thai FDA regulation and Quality requirements
1.3 Provide and support other requests related to RAQA in a professional and timely manner.
What you will learn from us:
- Product Registration and Notification
- Advertising MD – Collateral material review
- Importance of Quality
- Product Storage and Handling
- Complaint and Product Field Action
- Traceability and Records Retention
- A warehouse visit for local labeling and periodic walkthroughs is crucial for maintaining efficient warehouse operations.
Pay rate will not be below any applicable local minimum wage rates.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology and Orthopaedics that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
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