- 0-2 years of experience in IVD regulatory affairs.
- Bachelor's degree in a life science field.
- Proficient use of Microsoft Office applications (e.g., Excel, Word, PowerPoint, Teams).
- Previous laboratory research experience in an IVD medical device regulated environment.
- Provide regulatory support for IVD products within clinical diagnostics.
- Collaborate with various teams including Marketing, R&D, QA, Planning, and Manufacturing.
- Prioritize tasks, demonstrate flexibility, and manage multiple projects efficiently.
- Apply technical knowledge to grasp IVD product functionalities.
- Bachelor of Science in Biology with a focus on biology.
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Reg Affairs Specialist - Hercules, United States - Entegee
Description
Job Description
Summary: We are in search of a Regulatory Affairs Specialist with 0-2 years of experience in IVD regulatory affairs to provide regulatory support for IVD products within clinical diagnostics.
Job Requirements:
Preferred Skills:
Job Responsibilities:
Education:
Pay Details: $26.00 to $34.00 per hour
Our benefits package includes medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, commuter benefits, and a 401K plan. Employees can choose coverage that suits their needs. Paid leave options are available, including Paid Sick Leave and Holiday pay, where applicable.
Equal Opportunity Employer/Veterans/Disabled