Validation Lead in Corporate IT. HOVEDSTADEN. Dinamarca
Ofertas de trabajo de Analistas de sistemas en HOVEDSTADEN (Dinamarca)
Clasificación del trabajo:Profesionales científicos e intelectuales : Profesionales de tecnología de la información y las comunicaciones : Desarrolladores y analistas de software y multimedios : Analistas de sistemas. Arbejde, der forudsætter viden på højeste niveau inden for pågældende område : Arbejde inden for informations- og kommunikationsteknologi : Udvikling og analyse af software og applikationer : Systemanalytikerarbejde.
Descripción de la oferta de trabajo:
-?IT -?Denmark - Bagsværd Are you an experienced validation responsible with quality mind-set? Are you ready to take responsibility in supporting simplification of validation by driving it in agile development? Then join us as our new Validation Lead. About the department You get the opportunity to join an international, high performing team called Quality Solutions in Bagsværd, Denmark, responsible for managing a GxP Critical IT Platform, novoGloW. This platform has 8 applications, each of which support various Novo Nordisk quality processes. In this department, we define the strategy & technical specifications for novoGloW, provide support and implement changes/releases in accordance with ITIL, mature and develop changes & system configurations and ensure the platform & applications are in compliance. The position As our new Validation Lead, you will be trusted to drive the validation track in novoGloW releases, as a primary responsibility. You will work with global stakeholders including System & Release Managers, Quality Assurance (QA) and Test Managers, which is why it is key that you have a global mind-set, possessing strong communication & validation skills. We will help you build your knowledge specifically in the area of driving validation in an agile development of changes. As the Validation Lead, you are also responsible for defining the validation strategy, validation planning and reporting in relation to specific releases, system corrections & change implementations that includes Validation Master Plan (VMP); Validation Plan (VPL); Quality Plan (QP); Quality Report (QR); Validation Report (VR); Validation Master Report (VMR). Additionally, the Validation Lead is accountable for the completion of the required deliverables defined in relation to the validation strategy including CR case and defined actions; IT Risk Assessment (System Impact Assessment, IT Quality Risk Assessment, IT Security Risk Assessment and IT Security plan); User Requirements Specification; Underlying design specifications; Design qualification; Qualification protocols; Qualification execution; Validation Deviations; Qualification Reports; Configuration Item List; Traceability Matrix; Supplier Management; Operation and Maintenance processes. Qualifications Qualified candidates will at least hold a BSc in a Science, IT, Technical or Engineering related field. You must have solid experience in validation of IT systems in life sciences. It is an add-on if you have any experience with validation in an agile development of IT systems. You must have strong written and verbal communication skills in English. Your ability to structure, plan and manage your work will be a key factor to your success. You must be able to work independently and excel in a dynamic, hands-on department where things move at a fast pace and changes come rapidly. Working at Novo Nordisk At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. Contact For further information, please contact Preeti Shrihari at +45 3077 7534. Deadline 15 June 2017.
Servicio de empleo de origen:AMS, Servicios Públicos de Empleo, Dinamarca.