Global Validation Lead

15000 人民币~20000 人民币/每月

刷新于 1 个月前
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48 申请
天津
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工作职责
Closing on: May 30, 2025Job Category: ITJob Type: Full TimeJob Location: TianjinCountry: ChinaWe are seeking an experienced Global Validation Lead to join Elos Global IT team to lead and execute validation activities for our digitalization projects and implemented global applications.Elos Medtech is a company in growth and in a transition phase. We are on the path of becoming a data-driven and digitalized Medtech company, focusing on building an eco-system of best of breed applications to support our business needs.As we evolve, it becomes increasingly crucial to maintain our digital ecosystem in a validated state. This is why we are seeking a Validation Lead who can ensure that our systems and processes adhere to stringent regulatory standards and software validation requirements according to ISO1348 5. By joining our team, you will play a pivotal role in safeguarding the integrity of our operations. We prioritize digitalization and here you will have a say in our direction and methods. Engage in interesting IT transformation projects, with a focus on Cloud and Integration Platform as a Service (iPAAS). Join us for a fulfilling role where you can contribute to our digitalization journey and be part of a dynamic team!ResponsibilitiesLead and execute validation activities in global projectsDefine validation strategyImpact assessmentsRisk assessments (regulatory and functional)Define test strategyDocumentationEvaluating if new releases require re-validationIf you have a passion for validation and find yourself in the above criterias, we want to hear from you! This is an exciting opportunity to lead the validation of critical global systems that will help us to drive our business forward and achieve our digitalization strategy.
职位要求
RequirementsBachelor’s degree in engineering, computer science or a related field5+ years of experience of Computer Software Validation (in a medical industry)Knowledge about MES, ERP, iPAAS.Experience from working in Life Science industry.Detailed knowledge of FDA Standard for electronic signatures and electronic records (21 CFR Part 11) as well as the GAMP 5 approach for Software validations.Fluent in English, both verbal and writtenExcellent communication, problem-solving, and decision-making skillsBonusExperience with Cloud System ValidationIn this role, occasional travel is required to support various projects and initiatives
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