Overview
Regulatory Affairs Specialist Jobs in Oak Brook, Illinois, USA at Katalyst CRO
Responsibilities
Investigate, maintain, and manage regulatory product certification claims data, databases, and documentation systems.
Ensure accurate data entries and effective database management.
Review technical documents to retrieve information with a high level of accuracy.
Maintain clear, concise documentation, with experience in documentation control and coordination.
Perform other duties and responsibilities as assigned.
Engage in meaningful work that contributes to product safety and compliance.
Collaborate with a diverse team of professionals.
Enhance your skills in regulatory affairs and documentation management.
Requirements
The ideal candidate will have strong attention to detail, excellent communication skills, and the ability to work independently and collaboratively.
5 years of experience in a similar position.
Strong written and verbal communication skills.
Advanced skills with Microsoft Excel, including an understanding of Macros, and proficiency in Microsoft Suite.
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Title: Regulatory Affairs Specialist
Company: Katalyst CRO
Location: Oak Brook, Illinois, USA
Category: Administrative/Clerical, Quality Assurance – QA/QC
