. - Develop and deliver progress reports, proposals, requirements documentation and presentations to various - audiences, including project team, sponsors, steering committee and key stakeholders. - Ensure that
in the aerospace industry you act as a Battery Assembly Technician (m/w/d). You will report directly to the "Battery Assembly Lead" and work with our production team. The battery assembly team handles all
und Prozessabläufen • Die Erstellung von monatlichen Reports und Prüfung der übermittelten Daten ist außerdem eine Routineaufgabe • Die Aktualisierung interner Arbeitsunterlagen und Pflege des SOP steht ebenfalls
of test locations based on operational requirements Maintain detailed records of test facility development projects and regularly report on key performance metrics, project progress, and budget
stakeholders, closely collaborating with integration and battery development teams to drive improvements. Manage certification documentation, including test reports, ensuring compliance with industry standards
Reports regarding baselines/plan dates and supports maintenance of timelines in the various systems Review and prepare tables from various benchmark databases in order to support the team members in the
stakeholders, closely collaborating with integration and battery development teams to drive improvements. Manage certification documentation, including test reports, ensuring compliance with industry standards
, and DO-311 Document test processes thoroughly, contributing to certification efforts through detailed reports and analysis Conduct theoretical analysis of test data to inform design improvements
key stakeholders Collaborate closely with integration and battery development teams to drive continuous improvements Manage certification documentation, ensuring all test reports comply with industry
reports to different audiences Fluent in English with excellent written and verbal communication skills
project progress and report on key performance indicators (KPIs) Conduct in-depth market research and analysis to identify trends, opportunities, and risks in the supply market Develop and maintain a
key stakeholders Collaborate closely with integration and battery development teams to drive continuous improvements Manage certification documentation, ensuring all test reports comply with industry
, thermal reports, electrical calculations, and system overviews Design and generate manufacturing drawings for harnesses, electrical cabinets, and mounting plates Design and modify test rig safety systems
, iSHARE and other PM-tools Support project quality by coordinating activities and ensure ITS process, such as configuration management, is observed Assist in drafting project reports Continuously
, and/or brochures, as appropriate to the program ·Maintains program/project records, researches information and gathers and computes various data; prepares special and/or one-time reports, summaries, or
workshops, and writing reports and business documentsExperience in managing flow of money and resources through an organization, and the need to get maximum value at each stage to achieve commercial
) SDS-PAGE, Western Blots, HPLC based assays (e.g. SE-HPLC, RP-HPLC, AIX-HPLC), glyco-profiling Prepare scientific reports detailing assay development and qualification studies or other analytical studies
von Ad-hoc-Anfragen und monatliche Erstellung von Reports. Vorbereitung von Verhandlungen: Vor- und Nachbereitung von Entgeltverhandlungen sowie Durchführung von Ausgleichsberechnungen mit Kostenträgern
aussagekräftige Reports für Konzerninterne- und externe Empfänger, insbesondere GuV und Verwaltungskosten Du analysierst und entwickelst kontinuierlich qualitativ hochwertiger Managementinformationen
in regulated pharmaceutical industry and/or engineering company with proven experience on planning CQV activities, leading large senior reports and high understanding/management of KPIs Strong knowledge of ISPE
defect reporting Analyzing data, creating relevant documentation (e.g. study protocols and reports) and presenting results in team meetings Taking part to projects related to all Systems Product Care
and administer complex reports, projects, documentation and correspondence, wich may also require collecting, organizing, and analyzing data Unsere Anforderungen Long-term professional Experience
solutions. Prepare detailed project documentation, reports, and presentations for stakeholders. Coordinate with cross-functional teams, including software developers, electrical engineers and manufacturing
based on scope of work and resource requirements Track, follow up and report on invoicing Develop and manage a detailed project schedule and work plan for a portfolio of projects Provide project updates
systems and pipe networks Presenting project details and technical information to colleagues and clients Writing reports Managing project budgets Keeping up to date with changes in regulatory legislation
interfaces to IT systems or MES Responsible for providing cGMP compliant processes and facilities suitable for FDA and global regulatory approval Generation of regular project reports, financial updates
validation activities, which will be used to prepare the related registration documentation Author or reviewer for routine validation protocols and reports, associated change controls and supports the
Are you looking for a challenge? That's what we offer! „IT for Finance“, als ein Teil der globalen Informationstechnik, gestaltet aktiv die Prozesskette „Record-to-Report“ für alle Produktions
features or bugs Work in an agile and international environment Work data-driven, based on reports and analyses for deriving actions that are truly oriented towards our customers' needs Who you are
and resource requirementsTrack, follow up and report on invoicingDevelop and manage a detailed project schedule and work plan for a portfolio of projectsProvide project updates on a consistent basis to
). This includes the day to day people management, work assignment, KPI/IKO evaluation, development plans and couching the team (9 direct and up-to 60 indirect reports); -Recovery management in case of
based on operational requirements. Maintain detailed records of test facility development projects and regularly report on key performance metrics, project progress, and budget adherence. Ihr Profil
based on operational requirements. Maintain detailed records of test facility development projects and regularly report on key performance metrics, project progress, and budget adherence. Ihr Profil
regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form
tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Applicants should have: A university degree in a health care or other scientific discipline or a
regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study sites and with client representativesDepending on client model there might
Conference on Harmonization (ICH) guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study
risk assessment (DIN EN ISO 12100), user manuals, thermal reports, electrical calculations, selection of cables and devices, electrical bill of materials and system overvies. Manufacturing drawings for
reporting - Monthly Management Report KPI’s (ie: On Time Delivery, On Time In Full, Out of Stock, Materials Slow Moving), DIO, …) - Managing your team - Develop talent Succession planning Performance
feature acceptance based on requirements Manage and prioritize bug reports and tickets from internal and external stakeholders and analyze business value using internal data sources Oversee the complete bug
feature acceptance based on requirements Manage and prioritize bug reports and tickets from internal and external stakeholders and analyze business value using internal data sources Oversee the complete bug
feature acceptance based on requirements Manage and prioritize bug reports and tickets from internal and external stakeholders and analyze business value using internal data sources Oversee the complete bug
. Located in our Gothenburg or Munich office, the Procurement Excellence Manager will report to the Senior Procurement Excellence Manager in Gothenburg. Traveling will be required in this role to visit
und Optimierung bestehender Reports und Dashboards zur Auswertung von CRM Daten und KPIs für verschiedene Stakeholder (Sales Manager, Regional Manager, Produktmanager, etc.). CPQ Support unserer Standorte beim
understanding of the role and potential for IT in a business context Proven ability to manage non-direct reports to achieve results and work in a multi-cultural multi
activities and educate less experienced colleagues in related areas. Monitor performance of the services you are responsible for and report results as required and agreed. Liaise with staff for the
activities and educate less experienced colleagues in related areas. Monitor performance of the services you are responsible for and report results as required and agreed. Liaise with staff for the
pest control process, keeping contact with external company, review external reports and initiates CAPAs as per the internal process/ limitsResponsible for the light intensity measurements, planning of
, conduct KPI variance reports, and ensure timely delivery to local management and the division controller. Accurate planning and forecasting, including scenario planning, are part of your duties, involving
in conducting audits, writing audit reports and analyzing audits. • Demonstrated ability to lead and manage multiple responsibilities. • Identify functional constraints and identify solutions. • Ability to