Resumes
Resumes
![Blair Focke Photo 1 Blair Focke Photo 1](/i/2672585c2f7e35d1734ce1ddf849d315.jpg)
Director Of Manufacturing, Plasma Fractionation
View pageLocation:
Durham, NC
Industry:
Biotechnology
Work:
Grifols - Raleigh-Durham, North Carolina Area since Jun 2011
Purification Technical Manager
Talecris Biotherapeutics, Inc. - Raleigh-Durham, North Carolina Area Dec 2008 - May 2011
Purification Technical Manager
Talecris Biotherapeutics, Inc. - Raleigh-Durham, North Carolina Area Apr 2006 - Nov 2008
Purification Technical Support Supervisor
Bayer HealthCare - Raleigh-Durham, North Carolina Area Nov 2003 - Mar 2006
Continuous Improvement Program Designer
Bayer HealthCare - Raleigh-Durham, North Carolina Area Nov 2002 - Nov 2003
Process Development Engineer
Purification Technical Manager
Talecris Biotherapeutics, Inc. - Raleigh-Durham, North Carolina Area Dec 2008 - May 2011
Purification Technical Manager
Talecris Biotherapeutics, Inc. - Raleigh-Durham, North Carolina Area Apr 2006 - Nov 2008
Purification Technical Support Supervisor
Bayer HealthCare - Raleigh-Durham, North Carolina Area Nov 2003 - Mar 2006
Continuous Improvement Program Designer
Bayer HealthCare - Raleigh-Durham, North Carolina Area Nov 2002 - Nov 2003
Process Development Engineer
Education:
University of Houston 1998 - 2001
MS, Chemical Engineering Rice University 1993 - 1997
BS, Chemical Engineering
MS, Chemical Engineering Rice University 1993 - 1997
BS, Chemical Engineering
Skills:
Gmp
Process Simulation
Validation
Fda
Biopharmaceuticals
Biotechnology
Purification
Capa
Pharmaceutical Industry
Protein Purification
Change Control
Aseptic Processing
Sop
21 Cfr Part 11
Technology Transfer
V&V
Quality System
Lean Manufacturing
Manufacturing
Vaccines
Glp
Chromatography
Filtration
Process Engineering
Gxp
Computer System Validation
Process Improvement
Protein Chemistry
Chemistry
Lims
Continuous Improvement
R&D
Software Documentation
Hplc
Troubleshooting
Formulation
Design of Experiments
Process Optimization
Lifesciences
Ultrafiltration
Commercialization
Engineering
Root Cause Analysis
Cleaning Validation
Quality Auditing
Chemical Engineering
Operation
Process Development
Standard Operating Procedure
Process Simulation
Validation
Fda
Biopharmaceuticals
Biotechnology
Purification
Capa
Pharmaceutical Industry
Protein Purification
Change Control
Aseptic Processing
Sop
21 Cfr Part 11
Technology Transfer
V&V
Quality System
Lean Manufacturing
Manufacturing
Vaccines
Glp
Chromatography
Filtration
Process Engineering
Gxp
Computer System Validation
Process Improvement
Protein Chemistry
Chemistry
Lims
Continuous Improvement
R&D
Software Documentation
Hplc
Troubleshooting
Formulation
Design of Experiments
Process Optimization
Lifesciences
Ultrafiltration
Commercialization
Engineering
Root Cause Analysis
Cleaning Validation
Quality Auditing
Chemical Engineering
Operation
Process Development
Standard Operating Procedure
Languages:
English
German
German