Dorothée Philippe
Vrije Universiteit Brussel
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Dorothee Philippe is a highly experienced professional with 18.4 years of work experience in regulatory affairs, vaccines, and regulatory submissions in the pharmaceutical industry. She has expertise in GMP, quality systems, GXP, and CAPA, as well as knowledge in change control and quality assurance. Currently, she serves as the Director of Regulatory Affairs at IBA in Brussels, Belgium. Prior to this, she held various leadership positions at GSK in the United Kingdom, including Head of Quality Assurance and Global QA. Dorothee Philippe has a strong background in the pharmaceutical industry and has worked with renowned companies like GSK and GE Healthcare.
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About
Director Regulatory Affairs at IBA
Work Experience
director regulatory affairs at iba
Medical Equipment Manufacturing
Dorothée Philippe's Professional Milestones
- Senior Manager, Worldwide Vaccine Registration - Regulatory Affairs (2005-06-01~2010-09-01): Established and streamlined global vaccine registration process, ensuring compliance and mitigating risks for the global organization.
- Head Of Quality System Capability Team, Global Qa - Quality Assurance (2012-04-01~2015-08-01): Improving the quality system capabilities and implementing robust quality assurance strategies in the global QA field.
Education
Masters
1988-1993Skill
Regulatory Affairs
Vaccines
Regulatory Submissions
Pharmaceutical Industry
Gmp
Quality System
Gxp
Capa
Change Control
Quality Assurance
Biotechnology
Sop
Biopharmaceuticals
21 Cfr Part 11
Change Management
Fda
Clinical Trials
Validation
Certification
Colleagues
Other Named Dorothée Philippe
Frequently asked questions
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Dorothée Philippe works for IBA
Dorothée Philippe's role in IBA is director regulatory affairs at iba
Dorothée Philippe works in the industry of Medical Equipment Manufacturing
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Dorothée Philippe's latest job experience is director regulatory affairs at iba at IBA
Dorothée Philippe's latest education in Vrije Universiteit Brussel