Mario Sampedro Email & Phone Number | I am a quality leader with expertise in managing people in various quality functions in medical devices and Pharmaceuticals. I do this by fostering team collaboration to build trust and respect. I have been successful because I have a great understanding of quality regulations, a strong sense for compliance and make good decisions. What makes me unique is I bring a common sense approach to quality and have great troubleshooting skills. Throughout my career have gained Quality experience and led people in Quality Control, Quality Assurance, Product Quality Assurance, Complaint Investigations, Stabilities, Manufacturing Quality, Pharma Quality, Operations Quality, Quality Systems, Supplier Quality, CAPA and Audits in the Medical and Pharmaceutical Industries. My experiences are in FDA Quality Systems and ISO 13458 regulations. The people I’ve led were various numbers of quality engineers, quality technicians, quality specialists, supplier quality engineers, CAPA specialists, and document control specialist. My work environment has always been FDA regulated and required strong compliance. In all my roles I supported various audits from third party regulatory agencies including FDA pre approval inspections, FDA QSIT audits, and FDA consent decree audits. Specialties: Quality Control, Quality Assurance, Immunodiagnostics, Good Manufacturing Practices, Quality Systems, Supplier Quality, Combination Drug Products, Compliance, Budget Management, Managing People, IT solutions, Process Validations, CAPA, Auditing, Device Tracking, 21 CFR 210/211/820/821, 21 CFR Part4, and ISO 13485.

Mario Sampedro

I am a quality leader with expertise in managing people in various quality functions in medical devi...
Hugo, Minnesota, United States

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Mario Sampedro’s Email mario.sampedro@diasorin.com

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Mario Sampedro’s Location Hugo, Minnesota, United States

Mario Sampedro’s Current Industry Diasorin

Mario Sampedro’s Prior Industry Medtronic | Abbott Laboratories

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Work Experience

Diasorin

Senior Manager, Product Quality Assurance

2023-06-01 00:00:00 - Present

Medtronic

Senior Quality System Manager

2020-04-01 00:00:00 - 2023-02-01 00:00:00

Abbott Laboratories

Senior Quality Assurance Manager

2002-01-01 00:00:00 - 2005-01-01 00:00:00

Skills

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FAQ About Mario Sampedro

Mario Sampedro is located at
Hugo, Minnesota, United States

Mario Sampedro is a I am a quality leader with expertise in managing people in various quality functions in medical devices and Pharmaceuticals. I do this by fostering team collaboration to build trust and respect. I have been successful because I have a great understanding of quality regulations, a strong sense for compliance and make good decisions. What makes me unique is I bring a common sense approach to quality and have great troubleshooting skills. Throughout my career have gained Quality experience and led people in Quality Control, Quality Assurance, Product Quality Assurance, Complaint Investigations, Stabilities, Manufacturing Quality, Pharma Quality, Operations Quality, Quality Systems, Supplier Quality, CAPA and Audits in the Medical and Pharmaceutical Industries. My experiences are in FDA Quality Systems and ISO 13458 regulations. The people I’ve led were various numbers of quality engineers, quality technicians, quality specialists, supplier quality engineers, CAPA specialists, and document control specialist. My work environment has always been FDA regulated and required strong compliance. In all my roles I supported various audits from third party regulatory agencies including FDA pre approval inspections, FDA QSIT audits, and FDA consent decree audits. Specialties: Quality Control, Quality Assurance, Immunodiagnostics, Good Manufacturing Practices, Quality Systems, Supplier Quality, Combination Drug Products, Compliance, Budget Management, Managing People, IT solutions, Process Validations, CAPA, Auditing, Device Tracking, 21 CFR 210/211/820/821, 21 CFR Part4, and ISO 13485.