Regulatory Affairs Specialist I - Clinical Diagnostics (IVD)
Hercules, CA 94547 | Hybrid (2 days on-site + 1 flexible day after 30 days)
$40/hr | 1-Year Contract - high potential to extend or convert
Join a top-tier biotech and medical manufacturing company at the forefront of clinical diagnostics.
Are you detail-oriented, organized, and ready to contribute to impactful regulatory work? Our client is seeking a Regulatory Affairs Specialist I to support global product registration and IVDR compliance for in vitro diagnostic (IVD) devices. You'll collaborate cross-functionally with Marketing, R&D, QA, and Manufacturing teams to ensure products meet regulatory requirements worldwide. Experience in the IVD industry is essential to support technical documentation, SOP improvements, and global submissions across multiple diagnostic product lines.
What You'll Do:
What You Bring:
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