IT Application Architect Senior Consultant | CIO Advisory
The chance to build a better future is right in front of you
Your Future With Us - Cosa troverai in KPMG
The chance to build a better future is right in front of you
Do Work That Matters...
regulatory authorities such as the European Medicines Agency (EMA) and Food and Drug Administration (FDA) to define development pathways
• Manage regulatory submissions including Investigational New Drug (IND), Biologics License Application (BLA), Marketing...
segregazione, audit trail, rispetto policy IT.
• Documentazione & knowledge base: procedure operative, configurazioni, manuali, FAQ e formazione utenti chiave.
Requisiti richiesti
• 6–10 anni di esperienza come Application Manager / Business Application...
Documentation File by preparing and maintain up to date the regulatory Product Application Files applicable for any new or modified Products. (e.g. EU-MDR Technical Documentation File, FDA 510(k))
Responsibilities include collaboration with Quality Engineering...
Business unit.
The work activities include drafting, managing, negotiating and processing international distribution agreements, HCP contracts and clinical study agreements, supply agreements, royalty agreements, consultancy agreements and agreements with...
Documentation File by preparing and maintain up to date the regulatory Product Application Files applicable for any new or modified Products. (e.g. EU-MDR Technical Documentation File, FDA 510(k))
Responsibilities include collaboration with Quality Engineering...
Business unit.
The work activities include drafting, managing, negotiating and processing international distribution agreements, HCP contracts and clinical study agreements, supply agreements, royalty agreements, consultancy agreements and agreements with...
composed by consultants and near-shore resources
• Adopt agile SCRUM methodology for team management
• Provide guidelines on adoption of proper Design Patterns
• Provide guidelines respecting the architectural design of the application (microservices...
Documentation File by preparing and maintain up to date the regulatory Product Application Files applicable for any new or modified Products. (e.g. EU-MDR Technical Documentation File, FDA 510(k))
Responsibilities include collaboration with Quality Engineering...
Business unit.
The work activities include drafting, managing, negotiating and processing international distribution agreements, HCP contracts and clinical study agreements, supply agreements, royalty agreements, consultancy agreements and agreements with...
CPL TAYLOR by Synergos srl - Ricerca e Selezione Personale Qualificato-Verona
negotiable based on experience
The Company
An international consulting firm that delivers digital solutions for the Life Sciences sector. Headquartered in Italy and operating since 2010, it supports pharma and biotech organisations across regulatory affairs...
rapid evolution of IT systems by building a complete range of services: from research and consulting to design and development' from system integration of leading vendor software solutions right up to application management' supporting clients step by...
CPL TAYLOR by Synergos srl - Ricerca e Selezione Personale Qualificato-Verona
between €50,000 and €55,000 + 10% MBO + corporate welfare + meal vouchers
The Company
Our client is an international consulting firm specialized in digital consulting and solutions for the Life Sciences sector, headquartered in Italy and active since...
Who we are
We are an environmental consulting company. What’s our purpose? We put nature at the heart of decision-making by developing science-based solutions.
We support public and private entities that want to improve the environmental, social...
start of their careers.
We are committed to unleashing your potential' so you can expect a structured learning path and rich hands
• on experience' including:
• Dedicated skill-building workshops &, internal consulting group project
• One day of work in...