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The Role:
- Create, manage, and ensure closure of daily regulatory blocks.
- Become an expert with the GTS tool for regulatory release of IVD products.
- Oversee IVD registrations, renewals, and channel partner business licenses.
Qualifications:
- University degree in Life-Science, Engineering, or Law.
- Significant regulatory experience with IVD/medical device regulations.
- Strong analytical, communication, and organizational skills.
What We Offer:
- Independent, collaborative work in a growth-oriented organization.
- Commitment to work/life balance and opportunities for growth.
- Comprehensive benefits including bonus, stock plan, insurance, pension, and healthcare.
Agilent
Agilent provides life science, diagnostic and applied market laboratories with instruments, services, consumables, applications and expertise. With 18,000 employees worldwide, the company fosters a culture of trust, respect, integrity, and inclusivity.