Dr. Martina Henk

Gruppenleitung QC Prozesskette Chemie (Chemische Rohstoffe, Inprozesskontrolle, Wirkstofffreigabe, incl. Analytische Entwicklung von NCEs, Life Cycle Management, Trouble shooting, Lieferantenqualifizierung, Dokumentenerstellung), 9 analytische Labore, 1 Referat, >130 MA

Late Stage Drug Substance Development” Analytical Development Germany

Method Development incl. analytical equipment life cycle management, centralized GC and elemental analysis services, qualification of reference materials)

Quality Control Service Functions” (incl. project management, method development, analytical transfer of new chemical entities (NCEs))

Quality Control Organic Synthesis” (incl. quality control of active pharmaceutical ingredients, intermediates and chemical raw materials, method development, sampling)

Quality Control Active Pharmaceutical Ingredients and Method Development”

HPLC Laboratory incl. quality control and method development

Analytical Documentation and Stability Testing of Active Pharmaceutical Ingredients and Related Substances

Analytical Documentation and Stability Testing of Active Pharmaceutical Ingredients and related substances

“Organic Chemistry” (responsible for practical training of undergraduate students, training seminars, lectures as deputy)

“Instrumental Analysis” (responsible for practical training of undergraduate students in liquid chromatographic and spectral analytical methods)

PhD Thesis: „Synthesis and reactivity of O-functionalized (Indol-3-yl)-ethenes as precursors of new functinalized [b]annellated Indoles and Carbazoles “