Frank Sievert
Suchst Du einen anderen Frank Sievert?
Fähigkeiten und Kenntnisse
Werdegang
Berufserfahrung von Frank Sievert
- Bis heute 9 Jahre und 5 Monate, seit März 2016Teva ratiopharm
Senior Director Global Technology Center
Authorisation to act Identification and implementation of innovative technologies to develop novel products with additional patients' benefit Conceptual design and development of Global Technology Center Implementation of additive manufacturing (2D/3D printing) as a tool for personalized dosing and adherence enhancement, digitalised manufacturing. This includes formulation and printer development. Public funding for additive manufacturing projects
42 reports (direct and indirect Budget Responsibility: 10 mio € Identification of future relevant generic products by evaluating innovator's development pipeline Ensure generic launch with expiry of basic patent. Design around prolonging originator's patents. Securing freedom to operate for own development by suitable measurements including own intellectual property Evaluation and establishment of new technologies International project teams Qualification as “Qualified Person” acc. AMG
- 3 Jahre und 9 Monate, Jan. 2007 - Sep. 2010
Head of Pharmaceutical Research
ratiopharm GmbH
Implementation of Pharmaceutical Research as a new unit for innovation and added valued products . Authorisation to act 5 heads of department and 1 project manager as direct reports, 46 indirect reports, internationally organized (India, Swizerland, Germany) Conceptional design and implementation of Pharmaceutical Research as a new unit for innovation and added valued products Identification of future relevant generic products by evaluating innovator's development pipeline
- 9 Jahre und 3 Monate, Okt. 1997 - Dez. 2006
Head of Formulation Development
ratiopharm GmbH
Authorisation to act 3 Scientists as direct reports, 15 indirect reports Budget: 1 mio € Key responsibilities: Formulation development for New Chemical Entities (NCE) Formulation development for generics Process optimization Trouble Shooting Clinical trial supply Head of production clinical trials according AMG § 14
- 1 Jahr und 10 Monate, Dez. 1995 - Sep. 1997
Head of Formulation Development
Klocke Pharma Service GmbH
Key responsibilities: Implementation of formulation development in the company Manufacturing of clinical trial samples Support of production with trouble shooting and process development
- 1 Jahr und 9 Monate, März 1994 - Nov. 1995
Assistant to the production management
Klocke Pharma Service GmbH
Reporting to Head of production Authorised to give instructions to production staff Key responsibilities: Production trouble shooting Creation of manufacturing documentation (GMP) In process control Process optimization
- 5 Jahre und 2 Monate, Jan. 1989 - Feb. 1994
Laboratory Manager
Schwarz Pharma
Formulation development Key responsibilities: - Formulation development of all dosage forms (solids, semi solids, liquids) - Manufacturing of clinical trial samples - Qualification according AMG §14 (“Herstellungsleiter”)
- 10 Monate, März 1988 - Dez. 1988
Pharmacist in several pharmacies
serveral public pharmacies
Pharmacist inseveral public pharmacies for holliday replacement of resposible pharmacist
Ausbildung von Frank Sievert
- 1985 - 1986
Bahnhofsapotheke (public pharmacy) and Pharma Hameln (contract manufacturer)
On-the-job-training for pharmacist's licence to practice
- 1981 - 1985
Pharmacy
Technical University of Braunschweig
- 1980 - 1981
Chemistry
University of Bielefeld
Sprachen
Deutsch
Muttersprache
Englisch
Fließend
Französisch
Grundlagen
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