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Stellenangebot User Support Director Job bei STADA Arzneimittel AG Job vom 07.03.2025 STADA Arzneimittel AG

Senior Director Regulatory Affairs- Specialty Development (f/m/d)

Bad Vilbel Führungs-/ Leitungspositionen Jobticket
MEHR[...] and One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Senior Director Regulatory Global Specialty/ Biosimilar Development (f/m/d) Bad Vilbel Germany (DE) Full- time Permanent Portfolio Product Development Professionals What you can [...] and translation into potential impact assessment on STADA Specialty and Biosimilar business You take care of the development and implementation on state- of- the art processes You are responsible for the identification and implementation of best- in- class tools to support the department and the team You are the go- to expert for all kind of global local Regulatory questions Deputy [...] Clinical, Devices, labelling, pre- approval inspections, etc. You have a proven track record as team leader either in line or matrix setting You bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally [...]
Stellenangebot User Support Director Job bei STADA Arzneimittel AG Job vom 07.03.2025 STADA Arzneimittel AG Senior Director Regulatory Affairs Global Portfolio (f/m/d) Bad Vilbel Führungs-/ Leitungspositionen Jobticket
MEHR[...] and One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Senior Director Regulatory Global Specialty/ Biosimilar Development (f/m/d) Bad Vilbel Germany (DE) Full- time Permanent Portfolio Product Development Professionals What you can [...] and translation into potential impact assessment on STADA Specialty and Biosimilar business You take care of the development and implementation on state- of- the art processes You are responsible for the identification and implementation of best- in- class tools to support the department and the team You are the go- to expert for all kind of global local Regulatory questions Deputy [...] Clinical, Devices, labelling, pre- approval inspections, etc. You have a proven track record as team leader either in line or matrix setting You bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally [...]
Stellenangebot User Support Director Job bei STADA Arzneimittel AG Job vom 07.03.2025 STADA Arzneimittel AG

Senior Director Life Science/ Regulatory Affairs (f/m/d)

Bad Vilbel Führungs-/ Leitungspositionen Jobticket
MEHR[...] and One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Senior Director Regulatory Global Specialty/ Biosimilar Development (f/m/d) Bad Vilbel Germany (DE) Full- time Permanent Portfolio Product Development Professionals What you can [...] and translation into potential impact assessment on STADA Specialty and Biosimilar business You take care of the development and implementation on state- of- the art processes You are responsible for the identification and implementation of best- in- class tools to support the department and the team You are the go- to expert for all kind of global local Regulatory questions Deputy [...] Clinical, Devices, labelling, pre- approval inspections, etc. You have a proven track record as team leader either in line or matrix setting You bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally [...]
Alle Regulatory Affairs Stellenangebote anzeigen
Stellenangebot User Support Director Job bei STADA Arzneimittel AG Job vom 07.03.2025 STADA Arzneimittel AG Senior Director Regulatory Management (f/m/d) Bad Vilbel Führungs-/ Leitungspositionen Jobticket
MEHR[...] and One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Senior Director Regulatory Global Specialty/ Biosimilar Development (f/m/d) Bad Vilbel Germany (DE) Full- time Permanent Portfolio Product Development Professionals What you can [...] and translation into potential impact assessment on STADA Specialty and Biosimilar business You take care of the development and implementation on state- of- the art processes You are responsible for the identification and implementation of best- in- class tools to support the department and the team You are the go- to expert for all kind of global local Regulatory questions Deputy [...] Clinical, Devices, labelling, pre- approval inspections, etc. You have a proven track record as team leader either in line or matrix setting You bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally [...]
Stellenangebot User Support Director Job bei STADA Arzneimittel AG Job vom 07.03.2025 STADA Arzneimittel AG

Global Specialty Development Senior Director Regulatory Affairs (f/m/d)

Bad Vilbel Führungs-/ Leitungspositionen Jobticket
MEHR[...] and One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Senior Director Regulatory Global Specialty/ Biosimilar Development (f/m/d) Bad Vilbel Germany (DE) Full- time Permanent Portfolio Product Development Professionals What you can [...] and translation into potential impact assessment on STADA Specialty and Biosimilar business You take care of the development and implementation on state- of- the art processes You are responsible for the identification and implementation of best- in- class tools to support the department and the team You are the go- to expert for all kind of global local Regulatory questions Deputy [...] Clinical, Devices, labelling, pre- approval inspections, etc. You have a proven track record as team leader either in line or matrix setting You bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally [...]
Stellenangebot User Support Director Job bei STADA Arzneimittel AG Job vom 07.03.2025 STADA Arzneimittel AG Pharmaceutical Regulatory Affairs Director- Global (f/m/d) Bad Vilbel Führungs-/ Leitungspositionen Jobticket
MEHR[...] and One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Senior Director Regulatory Global Specialty/ Biosimilar Development (f/m/d) Bad Vilbel Germany (DE) Full- time Permanent Portfolio Product Development Professionals What you can [...] and translation into potential impact assessment on STADA Specialty and Biosimilar business You take care of the development and implementation on state- of- the art processes You are responsible for the identification and implementation of best- in- class tools to support the department and the team You are the go- to expert for all kind of global local Regulatory questions Deputy [...] Clinical, Devices, labelling, pre- approval inspections, etc. You have a proven track record as team leader either in line or matrix setting You bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally [...]
Stellenangebot User Support Director Job bei STADA Arzneimittel AG Job vom 07.03.2025 STADA Arzneimittel AG

Senior Director Regulatory Affairs Global Specialty/ Biosimilar Development (f/m/d)

Bad Vilbel Führungs-/ Leitungspositionen Jobticket
MEHR[...] and One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Senior Director Regulatory Global Specialty/ Biosimilar Development (f/m/d) Bad Vilbel Germany (DE) Full- time Permanent Portfolio Product Development Professionals What you can [...] and translation into potential impact assessment on STADA Specialty and Biosimilar business You take care of the development and implementation on state- of- the art processes You are responsible for the identification and implementation of best- in- class tools to support the department and the team You are the go- to expert for all kind of global local Regulatory questions Deputy [...] Clinical, Devices, labelling, pre- approval inspections, etc. You have a proven track record as team leader either in line or matrix setting You bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally [...]
Stellenangebot User Support Director Job bei STADA Arzneimittel AG Job vom 07.03.2025 STADA Arzneimittel AG Senior Director Life Science/ Specialty Pharma Development (f/m/d) Bad Vilbel Führungs-/ Leitungspositionen Jobticket
MEHR[...] and One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Senior Director Regulatory Global Specialty/ Biosimilar Development (f/m/d) Bad Vilbel Germany (DE) Full- time Permanent Portfolio Product Development Professionals What you can [...] and translation into potential impact assessment on STADA Specialty and Biosimilar business You take care of the development and implementation on state- of- the art processes You are responsible for the identification and implementation of best- in- class tools to support the department and the team You are the go- to expert for all kind of global local Regulatory questions Deputy [...] Clinical, Devices, labelling, pre- approval inspections, etc. You have a proven track record as team leader either in line or matrix setting You bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally [...]
Stellenangebot User Support Director Job bei STADA Arzneimittel AG Job vom 07.03.2025 STADA Arzneimittel AG

Global Regulatory Affairs Senior Director (f/m/d)

Bad Vilbel Führungs-/ Leitungspositionen Jobticket
MEHR[...] and One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Senior Director Regulatory Global Specialty/ Biosimilar Development (f/m/d) Bad Vilbel Germany (DE) Full- time Permanent Portfolio Product Development Professionals What you can [...] and translation into potential impact assessment on STADA Specialty and Biosimilar business You take care of the development and implementation on state- of- the art processes You are responsible for the identification and implementation of best- in- class tools to support the department and the team You are the go- to expert for all kind of global local Regulatory questions Deputy [...] Clinical, Devices, labelling, pre- approval inspections, etc. You have a proven track record as team leader either in line or matrix setting You bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally [...]
Stellenangebot User Support Director Job bei STADA Arzneimittel AG Job vom 07.03.2025 STADA Arzneimittel AG Senior Director Regulatory Global Specialty/ Biosimilar Development (f/m/d) Bad Vilbel Führungs-/ Leitungspositionen Jobticket
MEHR[...] and One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA. Do you want to become part of a dynamic, international team and grow with us? Then apply now as: Senior Director Regulatory Global Specialty/ Biosimilar Development (f/m/d) Bad Vilbel Germany (DE) Full- time Permanent Portfolio Product Development Professionals What you can [...] and translation into potential impact assessment on STADA Specialty and Biosimilar business You take care of the development and implementation on state- of- the art processes You are responsible for the identification and implementation of best- in- class tools to support the department and the team You are the go- to expert for all kind of global local Regulatory questions Deputy [...] Clinical, Devices, labelling, pre- approval inspections, etc. You have a proven track record as team leader either in line or matrix setting You bring a Robust understanding of Biologics/ recombinant molecules, ideally also Biosimilars with you You are an experienced user of regulatory intelligence software, publishing tools and document management software (preparation of eCTDs) You are a strong communicator, both verbally [...]
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