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Fly-line - Geschäftsführung Stellenangebote, Geschäftsführer gesucht Fly-line
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1Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. The Senior Director, Cell Line Development for Cytiva is responsible for leading the viral vector cell line development business, driving continuous improvement and ultimately ensuring long-term business success. This position is part of the Viral Vector business unit in the Genomic Medicine Operating Company located in Cologne, Germany and will be on site.Partner-Anzeige25.05.2024Geschäftsführung
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1Deine Rolle Als Line Lead (w/m/d/x) trägst Du Verantwortung für eines unserer dynamischen Produktionsteams an unserem Standort Barleben bei Magdeburg. Du stellst mit deinem Team eine reibungslose und bedarfsgerechte Bestückung der Lebensmitteltüten für unsere Kochboxen sicher.Partner-Anzeige20.05.2024Geschäftsführung
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1Deine Rolle Als Line Lead (w/m/d/x) trägst Du Verantwortung für eines unserer dynamischen Produktionsteams an unserem Standort Barleben bei Magdeburg. Du stellst mit deinem Team eine reibungslose und bedarfsgerechte Bestückung der Lebensmitteltüten für unsere Kochboxen sicher.Partner-Anzeige20.05.2024Geschäftsführung
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1Deine Rolle Als Line Lead (w/m/d/x) trägst Du Verantwortung für eines unserer dynamischen Produktionsteams an unserem Standort Barleben bei Magdeburg. Du stellst mit deinem Team eine reibungslose und bedarfsgerechte Bestückung der Lebensmitteltüten für unsere Kochboxen sicher.Partner-Anzeige20.05.2024Geschäftsführung
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1• For our R&D Quality Management in Marburg we are currently looking for a: • Senior Manager, R&D Quality (m/f/d) – R-229349(fulltime / unlimited / non-tariff Level 7/ Expiration Date: 07.05.2024)What you can expect• Manage integration of R&D quality systems, policies and procedures in line with CSL Global Quality Management System (QMS) for Product Development• Develop and maintain Phase appropriate Quality systems• Provide Quality overisght to the Product Development organisation for New Product Introduction, encompassing CSL and CMO manufactured and tested clincial material for Phase 1 & 2 and Phase 3 (where determined)• Primary representative for R&D Quality in site quality management forums and discussions• Manage the R&D quality unit to provide change control, batch technical release, deviation management and risk management functions for Product Development in Marburg and Bern• Provide QA disposition on R&D deviations/CAPAs and Investigations for R&D clinical materials• Accountable for the QA team for the technical review and disposition of non- clinical toxicological material and clinical material• Management of the R&D self inspection schedule for R&D functional areas• Assist with 3rd Party Quality audits as required to support Product Development• Drive and implement Quality Continuous Improvement Projects• Develop and build strong business relationships with local and global quality sites where manufacturing operations and shared between sites.• Develop Quality Key Indicators with key PD stakeholders to ensure effectiveness of quality systems within Product Development• Attend and provide Quality oversight for Core Project Teams representing Quality for new Product Development projects as required• Manage performance and development of R&D Quality Advisors• Educate and inform R&D on international trends in quality and compliance in the pharmaceutical industry as they relate to biotechnology product development• Develop and implement “Quality on the Floor” culture• What you bring• Bachelor degree or Master degree• Experience in pharmaceutical manufacturing is highly desirable• Sound knowledge of GxP, domestic & international regulation, processes & registered condition• Experience and knowledge in the application of Quality Systems• Previous experience with personnel management• English language fluency, German language is a plus• If you are interested in this challenging position, please apply via our website.Partner-Anzeige25.05.2024Geschäftsführung
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1Critical to the success of this role is your ability to work with big data, develop think big initiatives, communicate findings in a clear and compelling way and work effectively as part of the team, raising the bar and insisting on high standard. The role can be based in: LUX (Luxembourg), LHR (London), LIN (Milan), , MUC (Munich) or MAD (Madrid). Key job responsibilitiesCreate innovative solutions using data and research to address wider challenges in your organisationTake a big-picture approach in your analysis of business operations, driving improvements across a range of teams and organisationsWork alongside senior leadership to establish and prioritise improvement programmes, seeing them through from start to finishEnhance operational performance on every programme in partnership with your stakeholdersA day in the life As Senior Programme Manager, you’ll drive and manage the implementation of creative, data-driven change in Amazon, leading improvement projects and programmes.Partner-Anzeige25.05.2024Geschäftsführung
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1The Quality Assurance Specialist (m/f/d) for Cytiva is responsible to support QA operations in the viral vector cell line development business. This position is part of the Viral Vector business unit in the Genomic Medicine Operation Company located in Cologne, will be hybrid and temporary for 24 months. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.Partner-Anzeige19.05.2024Geschäftsführung
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1Quality System Management SupportSupport the QSMR management – planning, organization and documentation, QSMR action trackingSupport the External Audit Management – planning, real-time audits, post-audit activitiesResponsible for Quality Systems topics such as, responding to audit findings, QMS document reviewsCAPA ManagementResponsible for CAPA activities to problem statements, root cause analysis, corrective and preventative actions, tracking of time lines, and establishing CAPA filesMonitor the effectiveness of the CAPA systemSupport or Conduct training on tool usage SMARTSOLVE, EDMS, MasterControlThe essential requirements of the job includeBachelors or Master´s degree in Engineering / Science fieldOver 6 years of experience in Quality Management Systems in a Pharma or Medical Device industryKnowledge of ISO 13485, IVDR, 21 CFR Part 820 and 11Excellent Quality Documentation skills (Good Documentation Practices)Ability to work independentlyEnglish Mandatory, German is beneficialIt would be a plus if you also possess previous experience inElectronic Documentation Management (GxP Tools, MS office)Exposure to Certification body / FDA audits At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology.Partner-Anzeige19.05.2024Geschäftsführung
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1YOUR RESPONSIBILITIESDevelop and execute local business strategy according with EMEA guidelines and deliver sustainable growth and significant share win based on a deep understanding of local market dynamics, future trends and competitive landscapeResearch and identify opportunities in line with strategic directives in order to generate sales, increase the installed base penetration, upsell existing contracts and expand the portfolio of solutions soldDefining yearly growth targets to Account Managers and/or Indirect Partners (Distributors, Resellers, Lead Finders), reporting monthly revenues and potential gaps vs. targets and support close gap actions in order to maximize businessProactively assesses, clarifies, and validates customer needs on an ongoing base and provide transparent feedback to upper management and Business UnitsGenerate and develop sales and solutions awareness through customer visits & solutions information, customer consultancies & workshops.Partner-Anzeige25.05.2024Geschäftsführung
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1you will have the opportunity toMaintain a culture of control and compliance with regards to financial controls and cost discipline to ensure accurate accounting records and compliance with local and Cytiva requirements in close collaboration with the rest of the Finance teamDevelop and maintain performance KPIs to drive growth and profitability for the Cevec’s portfolio, including orders, sales, pricing, margin, and market share; to frequently present the analysis of actuals vs planMonitor the progress on agreed initiatives, through relevant KPIs and Risks & Opportunities, to pro-actively recommend mitigation actions for any deviations from target performance metricsMaintain appropriate record keeping in line with Cytiva and local standards, supporting the statutory account and specific legal entity requirementsThe essential requirements of the job includeBachelor’s degree in accounting, finance, or business administration degree and minimum of 3 years of financial work experience developing forecasts and operating plans and leading business/finance reviewsStrong skills in financial systems / applications (i.e.Partner-Anzeige19.05.2024Geschäftsführung
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1What you’ll do The Regional Sales Manager develops and owns the growth plan for their assigned territory selling the Precision NanoSystems line of instruments, consumables and support services directly to life science segments such as biotech, pharma and academia. The Regional Sales Manager will collaborate with Account Manager (AM), Workflow Development Leader (WDL) their Field Application Scientists (FAS), Scientific Inside Sales Specialists and Service Sales Specialists to maintain and grow the territory.Partner-Anzeige19.05.2024Geschäftsführung
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1YOUR RESPONSIBILITIESBuild and maintain strong relationships to partner with leaders in our Operations function to understand needs, challenges and goals to translate into effective HR solutions in line with employment law, best practice, HR policies and DHR processes. Execute talent strategies to grow associate development, leadership and organizational capabilities while collaborating with key talent across the supported functionsProvide advice, guidance and coaching on a wide range of HR matters, including talent management, talent development, employee engagement, retention, performance management, recruiting support, onboarding, terminations, organizational development, diversity/equity/inclusion and compensationDevelop and track daily & visual management related to key HR metrics (retention, development, DE&I etc.), analyze people and talent related data to identify trends and opportunities for improvement, and provide insights and recommendations based on data analysis to support business decision-making.Partner-Anzeige19.05.2024Geschäftsführung
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1Das macht deinen Job als Experte (m/w/d) Informationsrisikomanagement ausDu verantwortest die Organisation und Einhaltung des Informationsrisikomanagements gemäß BAIT; hierfür führst du Informationsrisikoanalysen durch und pflegst das InformationsrisikoinventarIm Rahmen des Informationsrisikocontrollings und -managements entwickelst du die Methodik und Prozesse weiter und erstellst InformationsrisikoberichteZudem stimmst du dich eng mit weiteren 2nd-Line-Funktionen, insbesondere dem Business Continuity und Compliance Management sowie dem operativen Risikomanagement, abDu stellst sicher, dass die initiierten Maßnahmen zur Informationsrisikobehandlung eingehalten werden und überwachst den FortschrittDu analysierst die Ursachen etwaiger Schadensfälle und koordinierst sowie überwachst Verbesserungsmaßnahmen; dabei berichtest du an den InformationssicherheitsbeauftragtenDas bringst du mitHochschulabschluss (Bachelor) oder Ausbildungsabschluss mit Zusatzqualifikation (z.B.Partner-Anzeige14.03.2024Geschäftsführung