Hanne Jensen Email
Senior Quality Specialist, CMC Development QA SQID @ Lundbeck
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Hanne Jensen Location
- Copenhagen, DK
Hanne Jensen Work
- Senior Quality Specialist, CMC Development QA SQID @ (January 2025 - Present)
- Member of the Quality Team @ Spejderneslejr 2022 - SL2022 (September 2020 - October 2022)
- Principal Compliance Specialist @ (January 2020 - December 2024)
- Head Of Quality @ (January 2019 - December 2019)
- Head QP and RP and Manager Manufacturing Quality Assurance @ (February 2017 - January 2019)
- Senior Quality Specialist @ (October 2016 - February 2017)
- Senior Quality Manager, Global Supply Chain Quality @ (April 2012 - September 2016)
- QA Director @ Eurofins Pharma A/S (February 2012 - April 2012)
- QA Compliance Manager, GMP (Temp.) @ (August 2011 - February 2012)
- Member of the Quality team @ Jamboree Denmark 2012 (February 2011 - September 2012)
- Member of the board of and Medlem af hovedbestyrelsen for @ (February 2008 - May 2012)
- Director of Quality @ (May 2007 - October 2010)
- Consultant as Lead Auditor @ Danish Medical Devices Certification, DGM (May 2007 - March 2009)
- Lead auditor @ Danish Medical Devices Certification, DGM (January 2004 - April 2007)
- Senior Quality Specialist @ (January 1999 - January 2003)
- Quality Specialist @ (January 1993 - January 1999)
- Lead Assessor @ Danish Institute of Fundamental Metrology, DFM (July 1991 - November 1993)
Hanne Jensen Education
- The Copenhagen School of Design and Technology (KEA)
(Project management)
2010-2011 - NLP Huset
NLP Practitioner (NLP)
2003-2003 - Pathfinder Leadership Program
(Leadership)
2000-2001 - DTU - Technical University of Denmark
PhD (Analytical chemistry)
1984-1986 - University of Cambridge
Certificate of proficiency (English)
1984-1985 - DTU - Technical University of Denmark
MSc (Chemical engineering)
1978-1984 - Ballerup Gymnasium
Student (Matematisk-Fysisk linje)
1975-1978
Hanne Jensen Skills
- Quality System
- GMP
- Quality Auditing
- FDA
- ISO 13485
- Validation
- CAPA
- Quality Management
- Quality Assurance
- Pharmaceutical Industry
- SOP
- Regulatory Affairs
- Biotechnology
- GLP
- Medical Devices
- GxP
- V&V
- Biopharmaceuticals
- 21 CFR Part 11
- TQM
- Change Control
- Root Cause Analysis
- ISO
- Continuous Improvement
- Iso 9000
- Clinical Trials
- CRO
- Cross-functional Team Leadership
- GCP
- Pharmaceuticals
- cGMP
- ISO 14971
- Quality Control
- Software Documentation
- Lean Manufacturing
- Supplier Quality
- Manufacturing
- Process Improvement
- Aseptic Processing
- Technology Transfer
- Calibration
- Regulatory Submissions
- Regulatory Requirements
- GAMP
- LIMS
- ISO 17025
- Computer System Validation
- Project Management
- U.S. Food and Drug Administration (FDA)
- Corrective and Preventive Action (CAPA)
- Quality Systems
- Process Validation
- Accreditation
- Corrective and Preventive Action Capa
- Cross Functional Team Leadership
- u.s. Food and Drug Administration Fda
- u.s. Food and Drug Administration
- Corrective and Preventive Action
Hanne Jensen Summary
- Hanne Jensen, based in Copenhagen, DK, is currently a Senior Quality Specialist, CMC Development QA SQID at Lundbeck. Hanne Jensen brings experience from previous roles at Spejderneslejr 2022 - SL2022, Xellia Pharmaceuticals and Pharmaero ApS. Hanne Jensen holds a 2010 - 2011 The Copenhagen School of Design and Technology (KEA). With a robust skill set that includes Quality System, GMP, Quality Auditing, FDA, ISO 13485 and more. Hanne Jensen has 1 emails on RocketReach.
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