
Dr. Hans-Peter Kapprell
Fähigkeiten und Kenntnisse
Werdegang
Berufserfahrung von Hans-Peter Kapprell
- Current 2 years and 1 month, since May 2024
Licensed Practitioner
self-employed
In addition to my executive and scientific leadership experience, I am a licensed German Complementary Medicine Practitioner (Heilpraktiker) and Certified Micronutrient Specialist focused on orthomolecular medicine, applying evidence-based nutrient strategies to support health and well-being—complementing my diagnostics expertise and reinforcing my commitment to systems-based, preventive, and personalized medicine grounded in scientific rigor and advanced laboratory diagnostics.
- 4 years and 1 month, Apr 2020 - Apr 2024
Director R&D Product and Process Optimization
Abbott GmbH, Wiesbaden
Led R&D Product & Process Optimization, a multi-disciplined team of experts with scientific, technical, and quality expertise. Mission ensured that product designs are of high quality, safe and effective, met customers’ expectations and provided a competitive advantage. During the entire product life-cycle used as a LSS BLACKBELT state-of-the-art analysis techniques such as Lean Six Sigma principles for R&D product & process improvements.
- 1 year, Apr 2019 - Mar 2020Abbott in Deutschland
Director Assay Development Process Integration, R&D System Engineering
Leads Assay Development Process Integration within the R&D Systems Engineering. Encourages and creates a disciplined, interdisciplinary, and collaborative approach to systems engineering for ADD diagnostic systems. Further responsibilities are not limited to the development of new systems/assay products, continuous process improvements, creation of BI Solutions for efficiency assessments and the creation of an integrated and domain inclusive engineering approach.
- 1 year and 3 months, Jan 2018 - Mar 2019Abbott in Deutschland
Director R&D Data Analytics, Design & Processes
Leads and manages the R&D Data Analytics Design and Processes organization for ADD assay research & development across multiple sites. Responsible for supporting design quality assessments for new products using data analytics and business intelligence solutions to influence and support design decisions. Contributes to the continuous development and execution of the Product Development Process (PDP) and supports the ADD assay R&D teams including TPD products in the areas of Design Control.
- 5 years and 8 months, May 2012 - Dec 2017Abbott in Deutschland
Director Design Quality Research and Development
Leads the Research and development QA organization for ADD diagnostic reagents. Responsible for designing quality into new products to meet customers' needs and expectations. Encourages and promotes focus on the customer and a culture of continuos improvement.
R for: (1) Multiple R&D programs & on time and budget completion of assay launches (2) Strategic Pl. & Portfolio Mgtm (3) Leadership, guidance, monitoring of R&D project team activities & Design Transfers to Manufacturing (4) Maintenance of Design Control System (5) Leadership of cont.Product Improvements (6) Maintenance of effective external R&D Collaborations (7)Talent Mgtm – establish, maintain effective & motivated R&D project teams (8) Market support:Presentations and chairing at int'l conf.
Tasks included responsibility for development projects i.e. research and development activities for immunoassays on different instrument platforms for the following markers: HIV, HBV, HCV, and HEV, the maintenance and adherence to design control procedures, the lead of development teams and direct reports as well as budgetary functions.
Tasks included the management of multiple products transfer activities between different affiliates e.g. Abbott USA, Germany, Japan, Ireland and external OEM partners, the lead of several cross-function teams (functions included: research, development, regulatory, quality, labeling, marketing, medical affairs and manufacturing) and the management and lead of direct reports as well as budgetary management.
Responsibility included product support & manufacturing of enzyme immunoassays for Hepatitis (HCV and HEV), the lead of a technical team(s), leading and coaching of direct reports as well as budget management.
Responsibility included development of enzyme immunoassays (HIV), the lead of cross-functional team(s) and direct reports as well as management of budgetary.
- 1 year and 8 months, Jun 1989 - Jan 1991Abbott in Deutschland
Mgr for Manufacturing of Recombinant Proteins
Function included (1) Technology Transfers (purification & conjugations) from Abbott, USA to Germany, (2) Fermentation, manufacturing and purification of recombinant HIV and HCV proteins which served as targets for immunoassay development activities and (3) Management of a “rare reagents lab group”.
Ausbildung von Hans-Peter Kapprell
- 1 year and 2 months, Mar 1988 - Apr 1989
Muscle Cell Biology and Biochemistry
University of Arizona, Az USA
Proteases, worked on cardiac biomarkers (calpain and calpastatin) which have been recently thought to play a role in Alzheimer disease. The study was granted by the American Heart Association. 4 publications and muttiple presentation at int'l meetings/conferences.
- 4 years and 10 months, Jun 1983 - Mar 1988
Cell and Tumorbiology and Biochemistry
Cancer Research Center Heidelberg
Cell Biology, Molecular Biology, Immunology and Microbiology.
- 1 year and 1 month, Jun 1982 - Jun 1983
Biology
Cancer Research Center, Heidelberg
Thesis: Cell Biology, Molecular Biology and Biochemistry at the Cancer Research Center in Heidelberg. The thesis was rated as outstanding.
- 3 years and 1 month, Jun 1979 - Jun 1982
Biology
Heidelberg
Biochemistry, Molecular Biology (Genetics), Organic Chemistry and Plant Physiology. All disciplines were rated as outstanding
- 1 year and 10 months, Sep 1977 - Jun 1979
Biology
University of Heidelberg
Zoology, Botanic, Organic Chemistry and Physics All disciplines wwere rated as outstanding
Sprachen
German
C2 (Verhandlungssicher / Muttersprachlich)
English
C1 (Fließend)
French
A1-A2 (Grundkenntnisse)
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