Regulatory Affairs Specialist
6 days ago
Transforming Healthcare through Regulatory Excellence
Baxter is a leading medical innovation company that has been pioneering significant medical breakthroughs for over 85 years. As a Regulatory Affairs Specialist, you will play a critical role in ensuring the compliance and quality of our products and therapies.
Key Responsibilities:
- Create and review regulatory documentation for Drug, Device, and Combination product renewals.
- Interact with non-regulatory support groups to request documentation necessary to support product renewals.
- Track status and progress of regulatory documentation that will be used for renewals.
- Coordinate and compile responses to regulatory authority renewal questions.
- Use an electronic document management system to compile documents to support product renewals for submission to Health Authorities.
- Answer internal queries for assigned products.
- Maintain a database of Regulatory Requirements for renewals.
Requirements:
- Knowledge of regulations.
- Scientific knowledge.
- Administrative and project management skills.
- Ability to contribute to multiple projects from a regulatory affairs perspective.
- Ability to multitask and prioritize.
- Interpersonal and communication skills.
- Technical system skills.
- Proofreading and editing skills.
About Baxter:
Baxter is a global leader in medical innovation, dedicated to improving healthcare outcomes for millions of patients worldwide. Our products and therapies are found in almost every hospital worldwide, in clinics, and in the home. We are committed to creating a workplace where our employees can thrive and make a meaningful impact.
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