SAP Solution Manager Consultant in Constanţa

SAP ABAP (nice to have) SAP Solution Manager (regular) SAP Solution Manager Consultant Requirements Very good quality management experience supporting large multi-site, global organizations in life science industry with significant exposure to requirements of ISO 13485, CFR 820, GMP, GDP, MDSAP, MDR, GRCStrong multiple end to end project lifecycle experience for implementing SAP business systems (ABAP skills would be an advantage)Solid Solution Manager experience Ability to promote high quality culture within the organization Experiences on execution of core quality activities: CAPA, management review, complaint, internal/third party audit, change control, documentation control, validation, traceabilityFamiliar Agile project implementation methodologies, hands-on project management experiences Experience in organizational change / process change and how to manage transformations is nice to haveSelf-driven personality with high analytical and conceptual thinking, excellent interpersonal skills, team player, goal-oriented, problem solving, negotiation, with the ability to perform in a complex, global environment Exceptional written and verbal communication skills Ability to work independently and in a team environment Responsibilities Quality Review of Solution Architecture Documents in Solution ManagerQuality Review and Approval of development Documentation in Solution Manager Quality Review and Approval of Customizing Documentation in Solution Manager Alignment and approval of transports in our SAP landscape according to CIT SOPs and PoliciesIndividual Technical Analysis of Developments (e.g. SAP) and make suggestions for improvementsPerform release planning for major and minor releases with project managersIdentify areas for RM improvements in architecture and implementationSupport & monitor the business process creation phase (Macros & Micros incl. quality attributes in Solution Manager)Prepare, align & communicate Refresh & Release schedules to global IT and BusinessEnsures that all quality system methodologies are in compliance with government regulations and relevant standards such as ISO 13485, CFR 820, GMP, GDP, MDSAP, MDR, GRCValidates quality processes by establishing quality system attributes; documenting evidenceWriting, updating and / or reviewing and approving QMS ProceduresPreparation, quality review and / or approval of release documentation in Solution Manager according to CSV WI and RACIPrepare, submit and present compliance methodology and documents to notified bodies like TüV, FDA, Financial Auditor, incl internal AuditsHelp update eQMS Policies, SOPs and WI's with respect to application lifecycle management Monitor Changes in quality and regulatory requirements and ensure efficient Implementation into respective processes and documentation Ensure adequate execution of core quality activities: CAPA, Management review, Complaint, internal / third party Audit, Change Control, Documentation Control, Validation, Traceability The offer An open corporate culture, supportive atmosphere High innovation pace and interesting med-tech products Cafeteria benefit system covering private medical care etc. Support in further training and development opportunities Modern office with comfortable working environment Onboarding program provided with close cooperation with your LM and the team Support in further training and development opportunitiesHybrid working model (2 days from the office) Office located in Warsaw


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