Expert Profile
Susan C Reilly
Principal, Reilly & Associates
Susan C. Reilly, Principal for Reilly & Associates, has over 20 years of quality assurance, quality engineering, and regulatory compliance experience in the medical device field. She is a recognized expert in the medical device industry, and is an ASQ Certified Quality Engineer, Quality Auditor, and Quality Auditor-Biomedical and an RAB QMS Provisional Auditor. Prior to becoming an independent consultant in 1999, she was Director, Quality Assurance and Compliance, at Medical Device Consultants, Inc. (MDCI) and Manager, Quality Assurance at Deknatel Division, Pfizer Hospital Products Group, Inc. Susan holds a B.S. degree in Chemical Engineering from The Pennsylvania State University. She is a senior member of the American Society for Quality and has held numerous Biomedical Division council and committee positions since 1991.
Trainings by Expert
Management Controls needed for an effective QMS to meet FDA QSR and ISO 13485 regulations
Category:
Medical Devices
,
All FDA Regulated Industry
,
Quality Management
,
Audits & Inspections
,
QMS, ISO 13485, CAPA
,
Supply Chain and Manufacturing
,
Audit & Inspection-Role
,
Medical Device Inspection
,
Life sciences QA/QC
,
Life Sciences
,
QA/QC
Internal Auditing Essentials for Medical Device Manufacturers to comply with FDA QSR and ISO13485
Category:
Medical Devices
,
All FDA Regulated Industry
,
Quality Management
,
FDA Audit and Inspection
,
Audits & Inspections
,
QMS, ISO 13485, CAPA
,
Supply Chain and Manufacturing
,
Audit & Inspection-Role
,
Medical Device Inspection
,
Life Sciences
Quality Management for FDA QSR and ISO13485 Compliance: Pack of Two Courses
Category:
Medical Devices
How to Manage an FDA Inspection
Category:
All FDA Regulated Industry
,
FDA Audit and Inspection
,
Audit & Inspection-Role
,
All FDA Reg. based Audit
,
Life Sciences
CAPA Essentials - core principles and practices needed to implement an effective and efficient CAPA process
Category:
Drugs and Chemicals (Pharma)
,
Medical Devices
,
Biotechnology
,
Quality and Safety
,
QMS, ISO 13485, CAPA
,
Laboratory
,
Quality & Safety
,
Life sciences QA/QC
,
Life Sciences
,
QA/QC
