Zarrin Chimeh
Regulatory Affairs Senior Specialist /EUMDR Project Manager | Regulatory Affairs I Medical Device l Biotechnology l Pharmaceutical
- Role
- Regulatory Affairs Senior Specialist at Medtronic
- Location
- Irvine, CA, US
- LinkedIn followers
- 500 followers
About Zarrin Chimeh
At BD, my role as a Senior Regulatory Specialist has centered on driving compliance across medical devices, leveraging my science background knowledge in medical device.Collaborating closely with regulatory agencies, I’ve been pivotal in submissions ranging from EUMDR Technical Files & working with Notified Body, to international registration. I have been a EUMDR project lead. My proficiency with tools like Sharepoint, MasterControl, RDMS, and RIM, empowers our collective success in the highly regulated medical device sector.
Experience
Regulatory Affairs Senior Specialist
Oct 2024 — Present
Education
Santa Clara University
Bachelor of Science (BS), Biology/Biological Sciences, General
Tehran University of Medical Sciences
Bachelor's degree, Health Care Management
2001 — 2005
California State University Channel Islands Extended University
Master of Science (MS), Biotechnology & Bioinformatics
Skills
- Hplc
- Cell Culture
- Bioinformatics
- Regulatory Affairs
- Managing Complex Sales
- Biotechnology
- Protein Purification
- Protein Extraction
- Molecular Modeling
- Microsoft Word
- Crystallography
- Molecular Biology
- Management
- Data Maintenance
- Powerpoint
- Microsoft Excel
- Toxicology
- Pcr
- Protein Chemistry
- Research
- Nmr Spectroscopy
- Customer Service
- Biopharmaceuticals
- Flow Cytometry
- Administrative Assistance
- Immunogenicity
- Dna Sequencing
- Dna Extraction
- Project Management
- Genomics
- Math Tutor
- Tissue Culture
- Proteomics
- Outlook
- Science
- Office Management
- Biochemistry
- Distillation
- Microsoft Office
- Managing Accounts
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