Thorsten Cech

Angestellt, Manager European Pharma Application Lab, BASF SE

Ludwigshafen, Deutschland

Fähigkeiten und Kenntnisse

Galenical development: Nasal sprays
syrups
granules
tablets
lozenges
effervescent tablets
MR formulations
ODTs
film-coated tablets
solubility enhancement
analytical testing
stability
packaging Granulation: Wet: fluid bed granulati
high shear granulation Dry: slugging
roll compactions Tableting: Single punch and ro
MR
SR in drum and fluid bed coaters Hot-Melt-Extru
SR formulations
grinding
milling and tableting; incl. analytical testing
granulation
tableting
film-coating
syrups Customer support: Supporting the custome
either at the customer’s or at BASF’s lab faciliti
with focus on BASF excipients
summarising and distributing the data. Training
articles
presentations
etc.) Presentations: Presenting lab and applica
seminars
conferences and at customers’ Engineering compa
Hüttlin
IMA
Innojet
Kilian
Manesty. Project management: Set up joined scie
universities and customers to gain application dat
case studies and publications Personnel managem
vocational trainees
diploma students

Werdegang

Berufserfahrung von Thorsten Cech

  • Bis heute 18 Jahre und 9 Monate, seit Sep. 2005

    Manager European Pharma Application Lab

    BASF SE

    Responsible for the technical support of BASF's Pharma customers in the Region Europe (Europe, Africa, West-Asia). This activity includes: formulation development of pharmaceutical dosage forms, process optimisation (incl. up-scaling), on-site support at customers, workshops (hosted by BASF, collaboration partners (such as engineering companies), customers), scientific presentations (e.g. on products (excipients), processes, ...) at workshops, seminars and conferences, writing of scientific publications

  • 4 Jahre und 11 Monate, Okt. 2000 - Aug. 2005

    Technical Assistant

    Boehringer Ingelheim Pharma GmbH & Co. KG

    Galenical development of solid and liquid pharmaceutical dosage forms for the OTC market. Responsibilities: process scale-up, transfer of developed products to various production sites, process validation, stability testing.

  • 4 Jahre und 3 Monate, Juli 1996 - Sep. 2000

    Technical Assistant

    Soliqs

    Galenical development of solid oral dosage forms (OTC and NCE) by means of hot melt extrusion (HME). Responsibilities: formulation development, product transfer to production (up-scaling), process validation, clinical samples

  • 3 Jahre und 1 Monat, Juni 1993 - Juni 1996

    Chemical Laboratory Technician

    Knoll AG

    Molecular Pharmacology and Screening

Sprachen

  • Deutsch

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