Resumes
Resumes
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Director Of Quality And Regulatory Affairs, Microbiology Business
View pageLocation:
Honolulu, HI
Industry:
Medical Devices
Work:
Beckman Coulter
Director of Quality and Regulatory Affairs, Microbiology Business
Beckman Coulter
Director of Quality Systems and Compliance
Siemens Healthcare May 2012 - Jan 2015
Director Quality Systems and Compliance
Siemens Healthcare Aug 2008 - May 2012
Senior Manager, Quality Systems, Compliance and Quality Assurance
Affymetrix Jan 2007 - Aug 2008
Qa Manager
Director of Quality and Regulatory Affairs, Microbiology Business
Beckman Coulter
Director of Quality Systems and Compliance
Siemens Healthcare May 2012 - Jan 2015
Director Quality Systems and Compliance
Siemens Healthcare Aug 2008 - May 2012
Senior Manager, Quality Systems, Compliance and Quality Assurance
Affymetrix Jan 2007 - Aug 2008
Qa Manager
Education:
Humboldt State University 1986 - 1990
Bachelors, Bachelor of Science San Diego State University
Bachelors, Bachelor of Science San Diego State University
Skills:
Fda
Quality System
Quality Assurance
Medical Devices
Capa
Iso 13485
Gmp
Continuous Improvement
Iso
Quality Management
Quality Auditing
Biotechnology
Microbiology
Sop
Regulatory Affairs
Corrective and Preventive Action
Technology Transfer
Quality Systems
Documentation
Auditing
Standard Operating Procedure
Iso Standards
Lifesciences
Software Documentation
Design Control
U.s. Food and Drug Administration
Life Sciences
Qsr
Compliance
Diagnostics
Mdsap
Adverse Event Reporting
Internal Audit
External Audit
Management Review
Risk Management
Cross Functional Team Leadership
Change Control
Manufacturing
Management
Leadership
Verification and Validation
Manufacturing Operations
Validation
Quality System
Quality Assurance
Medical Devices
Capa
Iso 13485
Gmp
Continuous Improvement
Iso
Quality Management
Quality Auditing
Biotechnology
Microbiology
Sop
Regulatory Affairs
Corrective and Preventive Action
Technology Transfer
Quality Systems
Documentation
Auditing
Standard Operating Procedure
Iso Standards
Lifesciences
Software Documentation
Design Control
U.s. Food and Drug Administration
Life Sciences
Qsr
Compliance
Diagnostics
Mdsap
Adverse Event Reporting
Internal Audit
External Audit
Management Review
Risk Management
Cross Functional Team Leadership
Change Control
Manufacturing
Management
Leadership
Verification and Validation
Manufacturing Operations
Validation