Philippe Buthier

Founder, GMP Manufacturing Expert , Lecturer in Pharmaceutical Quality and Manufacturing Sciences
Buthier Consulting Services, Switzerland
Dr. Philippe Buthier is a Swiss- and French-qualified Pharmacist with over 25 years of experience in the pharmaceutical industry, specializing in Manufacturing Science & Technology (MSAT), global technology transfer, and GMP industrial operations.
He is the founder and principal consultant of BCS I – Buthier Consulting Services I, supporting pharmaceutical and biotech companies in end-to-end technology transfers, process validation (PPQ, CPV), control strategy definition (QbD), and regulatory CMC activities (Module 3). His expertise covers small molecules and biologics, including complex oral solid dosage forms, drug substances, drug products, and combination products.
Throughout his career, Philippe has held senior technical and leadership roles in international pharmaceutical companies, leading multi-site transfers, supporting regulatory inspections, and bridging development, manufacturing, quality, and regulatory functions. He is recognized for his pragmatic, data-driven approach and his ability to turn operational complexity into robust, sustainable manufacturing solutions across the product lifecycle.
In parallel, Philippe is actively involved in education as a lecturer in pharmaceutical quality and manufacturing sciences, contributing to academic and executive programmes in Switzerland.

Events/Masterclasses Philippe Buthier is currently speaking at

Pharma

Technology Transfer for Pharma Oral Solid Dosages & Biotechnology Products
19 – 20 May 2026
Online Live Stream | 9:00 CEST – 16:00 CEST
This course aims to address the real challenges faced by industry teams when transferring manufacturing processes, analytical methods, equipment or technologies between sites or organizations.

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Philippe Buthier
Founder, GMP Manufacturing Expert , Lecturer in Pharmaceutical Quality and Manufacturing Sciences
Buthier Consulting Services, Switzerland
Dr. Philippe Buthier is a Swiss- and French-qualified Pharmacist with over 25 years of experience in the pharmaceutical industry, specializing in Manufacturing Science & Technology (MSAT), global technology transfer, and GMP industrial operations.
He is the founder and principal consultant of BCS I – Buthier Consulting Services I, supporting pharmaceutical and biotech companies in end-to-end technology transfers, process validation (PPQ, CPV), control strategy definition (QbD), and regulatory CMC activities (Module 3). His expertise covers small molecules and biologics, including complex oral solid dosage forms, drug substances, drug products, and combination products.
Throughout his career, Philippe has held senior technical and leadership roles in international pharmaceutical companies, leading multi-site transfers, supporting regulatory inspections, and bridging development, manufacturing, quality, and regulatory functions. He is recognized for his pragmatic, data-driven approach and his ability to turn operational complexity into robust, sustainable manufacturing solutions across the product lifecycle.
In parallel, Philippe is actively involved in education as a lecturer in pharmaceutical quality and manufacturing sciences, contributing to academic and executive programmes in Switzerland.
Philippe Buthier
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