
Dr. Hedinn Valthorsson
Fähigkeiten und Kenntnisse
Werdegang
Berufserfahrung von Hedinn Valthorsson
- Current 3 years and 2 months, since Apr 2023Grünenthal GmbH
Head Global Analytical & Manufacturing Science
Scientific and organizational leadership of the AMS department within the Global Operations unit, including the role of Head of Quality Control (for clinical samples). The core task of the department is the technical advancement and problem-solving (Pharmaceutical and Analytical Development) for current market products in Grünenthal's global portfolio, including licensed or externally manufactured products. Additionally, internal R&D projects are undertaken.
- 1 year and 7 months, Sep 2021 - Mar 2023Bayer in der Schweiz
Sr. Product Supply Project Leader - External Manufacturing
Identified and evaluated Contract Manufacturers (CMO) for Bayer products to be transferred. • Evaluation and selection of CMOs for Bayer Products to be externalized. • Project Management of Technical Transfer with cross-functional team members
- 2 years and 11 months, Oct 2018 - Aug 2021
Business Continuity Management & Crisis Management
Novartis International AG
- 1 year and 1 month, Oct 2017 - Oct 2018
Technical Transfer Lead
Novartis Pharma AG
- 3 years and 4 months, Jun 2014 - Sep 2017
Head Manufacturing Science & Technology
Novartis Pharma AG
- 1 year and 1 month, Jun 2013 - Jun 2014
Director of Production Support
Novartis / Sandoz
- 11 months, Oct 2010 - Aug 2011
QbD Leader PharmOps CH
Novartis Pharma AG
Responsible for all QbD / PAT activities in Pharmaceutical Operations in Switzerland, including Sterile Manufacturing, BioPharmaceuticals and Solid Dosage Forms. Combine Operational Excellence with QbD and PAT, creating real Continual Improvement opportunities by creating regulatory flexibility for products and processes. Compliance expert, Working as part of a two man team taking full responsibility for quality assurance aspects of new product launches for the entire organisation.
Took responsibility for all aspects of the process from granulation to final packaging and testing. Led a multifunctional team comprising 70+ operators and engineers. Delivered targets and key performance indicators. Drove Lean production and Continual Improvement to remain competitive while maintaining regulatory compliance. Implemented Quality by Design (QbD) / Process Analytical Technology (PAT) into existing manufacturing processes (Real Time Release approved by regulatory authorities)
- 2 years and 4 months, Jan 2006 - Apr 2008
QbD/PAT Global Project leader
Novartis Pharma
Coordinated activities of a global team of +30 people. Developed a QbD strategy in tight collaboration with FDA (CRADA). Presented the Novartis QbD strategy to regulatory authorities (FDA/EMEA). Presented at multiple international conferences on QbD/PAT. Participated in ISPE’s PQLI team, publishing paper on QbD/PAT control strategy
Ausbildung von Hedinn Valthorsson
- 3 years, Feb 2003 - Jan 2006
Pharmaceutical Technology
University of Basel
- 4 years and 9 months, Sep 1997 - May 2002
Pharmacy
University of Braunschweig, Germany
Sprachen
German
C1 (Fließend)
English
C1 (Fließend)
Russian
B1-B2 (Gute Kenntnisse)
Danish
C1 (Fließend)
Icelandic
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