Manager of Intralogistics for Process Analyses & Standardization
Novo Nordisk
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Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading…CategorySelect how often (in days) to receive an alert:×Select how often (in days) to receive an alert:Manager of Intralogistics for Process Analyses & StandardizationCategory: ManufacturingLocation:Hillerød, Capital Region of Denmark, DKAre you a motivated and experienced manager ready to lead our initiatives in enhancing intralogistics processes and establishing robust global standards? Are you prepared to identify opportunities for process optimization globally, and to steer standardization efforts to scale production and enable automation?If you are a goal-oriented individual with a passion for process enhancement and standardization, we invite you to apply for the dynamic role.The positionAs the Manager of Intralogistics for Process Analyses & Standardization, your key responsibilities will be:Interpreting the Voice of the Business and converting it into User Requirement Specifications and other essential requirements within the intralogistics processes.Mapping and understanding intralogistics process.Identifying areas for standardization within intralogistics, including impact assessment of what it will take to implement the standard.Ensuring projects designing intralogistics solutions receive thorough feedback as they reach critical decision points in the PEM state/gate model.Instituting a standardized approach for applying the Intralogistics Maturity Model, a framework for assessing current capabilities and identifying areas for improvement in intralogistics processes.Steering the standardization efforts to harmonize and align throughout the organization, with the aim of scaling production and enabling automation.This role requires active engagement, an ability to generate solutions in challenging circumstances, and a cross-functional mindset.QualificationsTo succeed in this position, we imagine you have:Min. Bachelors in e.g. Natural Sciences, IT, EngineeringPrevious managerial experience and leadership capabilities.Experience in fostering process optimization and establishing industry standards.Proficiency in transforming business insights into actionable user requirements.Strong communication skills and proficiency in EnglishWorking in pharma or a similar regulated environment, as well familiarity with systems engineering, verification, and validation will be advantageous.On a personal level, you contribute positively to our department and enjoy working with people from different professional backgrounds. You work in a structured manner with a non-compromised focus on quality and deliverables.About the DepartmentDevice Manufacturing Development (DMD) is responsible of the industrialisation of all medical devices at Novo Nordisk. We are an end-to-end corporate organisation developing products for high volume production, establishing control strategy of the product, developing, and implementing the production equipment at the production site all over the world, and developing innovative and digital solutions to our processes.
Hillerød, Hovedstaden
Sat, 20 Jul 2024 05:06:24 GMT
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