Resumes
Resumes
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Capa Sme
View pageLocation:
206 Sinagoga Ln, Imperial, PA 15126
Industry:
Pharmaceuticals
Work:
Various Oct 2018 - Nov 2016
Quality and Compliance Consultant
Wockhardt Feb 2017 - Oct 2018
Director Quality Assurance
Validant 2015 - Feb 2016
Capa Sme
Pharma Tech Industries Jun 2013 - Apr 2015
Senior Director Qa
Validant Mar 2013 - May 2013
Qa Consultant
Quality and Compliance Consultant
Wockhardt Feb 2017 - Oct 2018
Director Quality Assurance
Validant 2015 - Feb 2016
Capa Sme
Pharma Tech Industries Jun 2013 - Apr 2015
Senior Director Qa
Validant Mar 2013 - May 2013
Qa Consultant
Education:
Georgia Institute of Technology 1987 - 1989
Indiana University of Pennsylvania 1984 - 1987
Master of Science, Masters, Chemistry St. Xavier's College 1980 - 1983
Bachelors, Bachelor of Science, Chemistry
Indiana University of Pennsylvania 1984 - 1987
Master of Science, Masters, Chemistry St. Xavier's College 1980 - 1983
Bachelors, Bachelor of Science, Chemistry
Skills:
Validation
Quality System
Change Control
Gmp
Quality Assurance
Pharmaceutical Industry
Capa
Fda
21 Cfr Part 11
Technology Transfer
Quality Auditing
Gxp
Glp
Sop
Cleaning Validation
Regulatory Affairs
Biopharmaceuticals
Pharmaceutics
Quality Management
Quality Control
Cross Functional Team Leadership
Lims
Analytical Chemistry
Trackwise
Fda Gmp
Chromatography
Vaccines
Cgmp Practices
Deviation Management
Contract Manufacturing
Hplc
Iso 13485
Regulatory Requirements
Deviations
Gamp
Root Cause Analysis
Auditing
Iso
Supplier Quality
Equipment Qualification
Raw Materials
Cgmp Manufacturing
Iso 9000
Usp
Pharmaceutical Manufacturing
Batch Release
Nda
Manufacturing Operations
Thrive In A Fast Paced Environment
Enjoy Challenges
Quality System
Change Control
Gmp
Quality Assurance
Pharmaceutical Industry
Capa
Fda
21 Cfr Part 11
Technology Transfer
Quality Auditing
Gxp
Glp
Sop
Cleaning Validation
Regulatory Affairs
Biopharmaceuticals
Pharmaceutics
Quality Management
Quality Control
Cross Functional Team Leadership
Lims
Analytical Chemistry
Trackwise
Fda Gmp
Chromatography
Vaccines
Cgmp Practices
Deviation Management
Contract Manufacturing
Hplc
Iso 13485
Regulatory Requirements
Deviations
Gamp
Root Cause Analysis
Auditing
Iso
Supplier Quality
Equipment Qualification
Raw Materials
Cgmp Manufacturing
Iso 9000
Usp
Pharmaceutical Manufacturing
Batch Release
Nda
Manufacturing Operations
Thrive In A Fast Paced Environment
Enjoy Challenges