Rose Buot Email & Phone Number
Bioprocessing Division and Head of Quality, Senior Director Quality @ Purolite Healthcare & Life Sciences
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Rose Buot Location
- Bristol, England, GB
Rose Buot Work
- 2024 -now Bioprocessing Division and Head of Quality, Senior Director Quality @
- 2023 -2024 Exe;Director Quality Bioprocessing @
- 2020 -now Ex Director Quality and Technical Dept Management @ Pharmaceutical
- 2019 -2022 Exec Director : Quality and compliance @
- 2017 -2019 Global Head Quality Dept (VP) Animal Health Division, Vaccines, pharmaceutical products @
- 2015 -2019 Senior Director Quality and Compliance and EHS @ Biotechnology Cancer and Vaccine
- 2012 -2015 QA Director GxP @ Covance Laboratories
- 2010 -2011 Vice President Quality and Compliance @ Clearstone Central Labs
- 2006 -2010 Project Director @
- 2002 -2006 Global QA Manager GxP @
- 2001 -2002 Project Director: Equipment Qualification ; validation Methods and CSV @ Technip-Coflexip: A Consultant assigned at CISBIO (Central Energy Atomic, Diagno
- 1995 -2001 GMP and GLP Manager (GCP auditor) @ INNOTHERA-Plebology and Contention
- 1994 -1994 Interne Analytical Developement Laboratory @ Laboratoire de Dévelopment Analytique- Facuté de Pharmacie de Chatenay-Malabry
- 1993 -1993 QA interne @ Institut Pasteur Paris
Rose Buot Education
- University of Brigton UK (United Kingdom)
Qualified Person_PGDip Industrial Pharmaceutical studies
2015-2017 - Conservatoire National des Arts et Métiers
Ph.D degree
2006-2012 - Conservatoire National des Arts et Métiers
Ingénieur
1997-1999 - Université Paris XI FAculté de Pharmacie
Master Degree II
1994-1996 - Faculté de Pharmacie Paris XI
Master de degree I
1993-1994
Rose Buot Skills
- Auditing
- Quality Management
- Clinical Trials
- Buildings
- Api and Gmp
- CRO
- Intellectual Property Valuation
- Expert Qa and Risk Assessment Based
- Computer System Validation
- HPLC
- Chemistry
- Root Cause Analysis
- cGMP
- GMP
- Bpl
- Process Validation
- GxP
- Clinical Research
- Advance Knowledge on Gcp
- Biotechnology
- Change Control
- Regulatory Affairs
- Life Sciences
- Validation
- Process Improvement
- Quality Assurance
- Compliance
- Pharmacovigilance
- Quality System
- Lifesciences
- Advance Knowledge on Validation Csv and Methods
- Clinical
- Pharmaceuticals
- GCP
- Quality Auditing
- Pharmaceutics
- Manufacturing
- Clinical Development
- u.s. Food and Drug Administration Fda
- Quality Control
- Intellectual Property
- Pharmaceutical Industry
- Aseptic Processing
- Continuous Improvement
- GLP
- CAPA
- R&d
- FDA
- Sop
- 21 CFR Part 11
- Biopharmaceuticals
- u.s. Food and Drug Administration
- Advance Knowledge on Validation
Rose Buot Summary
- Rose Buot, based in Bristol, England, GB, is currently a Bioprocessing Division and Head of Quality, Senior Director Quality at Purolite, An Ecolab Company. Rose Buot brings experience from previous roles at Purolite, An Ecolab Company, Pharmaceutical, Ethypharm and BENCHMARK ANIMAL HEALTH LIMITED. Rose Buot holds a 2015 - 2017 Qualified Person_PGDip Industrial Pharmaceutical studies @ University of Brigton UK (United Kingdom). With a robust skill set that includes Auditing, Quality Management, Clinical Trials, Buildings, Api and Gmp and more. Rose Buot has 2 emails and 2 mobile phone numbers on RocketReach.
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