Orthopedic devices researcher with 3-year experience in an industrial research/service organization. Experienced in the product realization process, FDA 510(k) clearance, quality system and pilot production in the Biomaterial Production GMP. Strong analytical, logical thinking and detail-oriented.
Specialties:
ISO 13485, 10993, 14971
Quality System Development
Research/pilot Plant Management
Risk management, control and analysis
Negotiation with regulators
Minimally invasive surgical procedures
Implantable devices
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