Myron F Civils from 32 Waters Edge Ln E, Oriental, NC 28571, age 73

Myron Civils Phones & Addresses

32 Waters Edge Ln E, Oriental, NC 28571
Cove City, NC
784 Silverleaf Dr, Greenwood, IN 46143 • (317)8518409
Burr Ridge, IL
Dublin, OH
Romeoville, IL
Indianapolis, IN
Schenectady, NY

Work

Company:

Eli lilly and company
Jul 2012
Position:

Senior consultant

Education

Degree:

MS
School / High School:

East Carolina University
1971 to 1978
Specialities:

Biology / BA, Biology/Microbiology / BA, Psychology

Skills

Validation • Fda • Gmp • Pharmaceutical Industry • V&V • Capa • Quality System • Medical Devices • Sop • Sterilization • Cleaning Validation • Aseptic Processing • Quality Assurance • Biotechnology • Regulatory Affairs • Quality Control • Change Control • 21 Cfr Part 11 • Technology Transfer • Manufacturing • Pharmaceutics • Microbiology • Iso 13485 • Computer System Validation • Science • Process Improvement • Quality Management • Sterility Assurance • Regulatory Requirements • Biopharmaceuticals • Lims • Laboratory • Gxp • Glp • Gamp • Analysis • Drug Development • Clinical Trials • Cross Functional Team Leadership • R&D • Regulatory Submissions • Quality Auditing • Life Sciences • Change Management • Lifesciences • Risk Assessment

Interests

Gamma/Eo/Steam/Dry Heat Sterilization • Aseptic Pharma Filling • Cleaning Validation • Risk Assessments • Microbiology

Emails

h***[email protected]

Industries

Pharmaceuticals

Resumes

Senior Consultant

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Location:

32 Waters Edge Ln, Oriental, NC 28571

Industry:

Pharmaceuticals

Work:

Eli Lilly and Company since Jul 2012
Senior Consultant
Eli Lilly May 2004 - Jun 2012
Validation Advisor
PharmTech Consulting Firm Jun 2003 - Apr 2004
Consultant
PharmTech, Inc. 2003 - 2004
Pharmaceutical Consultant
Sterigenics / IBA Mar 1999 - Jun 2003
Technical Director Consulting

Education:

East Carolina University 1971 - 1978
MS, Biology / BA, Biology/Microbiology / BA, Psychology

Skills:

Validation
Fda
Gmp
Pharmaceutical Industry
V&V
Capa
Quality System
Medical Devices
Sop
Sterilization
Cleaning Validation
Aseptic Processing
Quality Assurance
Biotechnology
Regulatory Affairs
Quality Control
Change Control
21 Cfr Part 11
Technology Transfer
Manufacturing
Pharmaceutics
Microbiology
Iso 13485
Computer System Validation
Science
Process Improvement
Quality Management
Sterility Assurance
Regulatory Requirements
Biopharmaceuticals
Lims
Laboratory
Gxp
Glp
Gamp
Analysis
Drug Development
Clinical Trials
Cross Functional Team Leadership
R&D
Regulatory Submissions
Quality Auditing
Life Sciences
Change Management
Lifesciences
Risk Assessment

Interests:

Gamma/Eo/Steam/Dry Heat Sterilization
Aseptic Pharma Filling
Cleaning Validation
Risk Assessments
Microbiology

Myron F Civils