hays-searchresults-alternative-title
hays-searchresults-alternative-subtitle

Bundesland Wien | Freiberuflich für ein Projekt | hays-searchresults-startdate | 430263/1
Koordination zweier Projekte Konzepterstellung einer Personalschleuse sowie einer Produktionsschleuse (Feuchtgranulierungsbereich) und der zusätzlichen Erneuerung eines Granulierers Eigenständige Angebotserstellung, Lieferantenauswahl bis hin zur Betreuung des Schleusenbaus
Bundesland Wien | Freiberuflich für ein Projekt | hays-searchresults-startdate | 427430/1
Koordination eines Teilprojektes im Bereich "Fill & Finish" (aseptische Impfstoffe im Bereich der Tiergesundheit) Koordination des Aufbaus einer neuen Pharma-Anlage (Planungsumsetzung) Erstellen von Ausschreibungsunterlagen und Vergleichen von Lieferantenangeboten hinsichtlich technischer Punkte (unter Berücksichtigung der Kundenanforderungen) Zuständig für die Standardisierungen, Normen and Review Meetings Dokumentenfreigabe
Bundesland Niederösterreich | Freiberuflich für ein Projekt | hays-searchresults-startdate | 426859/1
Koordinative Unterstützung in der Planung und Durchführung eines QC-Labor-Umzuges Projektvorbereitungsarbeiten für durchzuführende Validierungen Koordinationsaufgaben im der Validierungsphase des Projekts Projekt Support für Validierung und Engineering „System Improvement“ - Erstellen von Standard-Dokumenten, Templates, etc. Erstellen von Dokumenten - URS, Spezifikationen, Validierungsdokumenten, etc.
Hessen | Freiberuflich für ein Projekt | hays-searchresults-startdate | 402297/1
Prozess Risikoanalyse über alle Prozesse im QM-System Identifizierung der zu validierenden Prozesse Aufbau Validierungsstrategie (Validierungsmasterplan) Aufbau Vorgabedokumente zur Prozessvalidierung (Herstellungsprozesse, Transportvalidierung) Aufbau Vorgabedokumente zur Computervalidierung und Life Cycle Management für neu und Bestandssysteme Erarbeiten der wichtigsten Validierungspläne (Prozess und CS) Durchführung Computervalidierung Erarbeitung einer Aufwandsschätzung zu den Validierungsaufwänden bei Ausbau der Organisation als Großhandel
Bundesland Wien | Freiberuflich für ein Projekt | hays-searchresults-startdate | 397000/6
Prozessbegleitung des Baus und der Inbetriebnahme Prozessbegleitung der Planungsphasen (Basic- und Engineeringphasen)
Hessen | Freiberuflich für ein Projekt | hays-searchresults-startdate | 390683/24
Durchführung einer Ist-Analyse Erstellung eines Konzeptes für den Versorgungshof Kostenanalyse und Kostenplanerstellung Anpassung des Konzeptes an Regularien/ Anforderungen
Baden-Württemberg | Freiberuflich für ein Projekt | hays-searchresults-startdate | 389692/1
Sicherstellung der Einhaltung von internen Standartanweisungen im Rahmen der Objektüberwachung Sicherstellung und Beratung bezüglich des Arbeits-, Gesundheits-, und Brandschutzes Abnahme und Teilabnahme der Leistungen von Auftragnehmern und Lieferanten Beratung der Fachbauleitung bezüglich Bau- und Errichtungsverfahren, Terminplänen und Qualitätssicherung Erstellung und Nachführung von Mängellisten Qualitätsstichproben
Bayern | Freiberuflich für ein Projekt | hays-searchresults-startdate | 386892/1
Erstellung von Risikoanalysen für Anlagen in der Produktion (z.B. Bioreaktoren und Reinstdampfanlagen) Erstellung von SIL-Risikographen (Sicherheits-Integritätslevel) Dokumentation
Basel | Freelance/temporary employment for a project | hays-searchresults-startdate | 430119/1
Accountable for the evidence generation strategy planning and execution, incl. (but not limited to) identifying medical and access gaps and needs as part of the overall Medical strategy Responsible for the joint planning and execution of the Medical Strategy for the assigned product(s) / indication(s) Drive and lead the strategy of the integrated evidence generation activities Accountability for evidence generation activities for the assigned product (s) / indication(s), including risk benefit assessment and medical monitoring in all medical Affairs interventional studies Take the role of Lead Scientific Responsible and act as a member of the Study Management Team (SMT) Assess the needs and coordinates compassionate use of the assigned product(s)
Basel | Freelance/Contracting project | hays-searchresults-startdate | 430124/1
Accountability for the evidence generation strategy planning and execution, incl. (but not limited to) identifying medical and access gaps and needs as part of the overall Medical strategy Responsible for the joint planning and execution of the Medical Strategy for the assigned product(s) / indication(s) Drive and lead the strategy of the integrated evidence generation activities Accountability for evidence generation activities for the assigned product (s) / indication(s), including risk benefit assessment and medical monitoring in all medical Affairs interventional studies Take the role of Lead Scientific Responsible and acts as a member of the Study Management Team (SMT) Assess the need and coordinates compassionate use of the assigned product(s
Basel Stadt | Freelance/temporary employment for a project | hays-searchresults-startdate | 427765/1
Being an expert in emerging oncology agents, modalities, and drug discovery platforms Lead or influence key internal development and commercialization decisions Drive translation of competitive findings into business recommendations that deliver success for the organization Data expert to assure that impactful, actionable competitor information and Roche product differentiation is identified and taken into account during key decisions via strategic workshops or other venues Identify opportunities to improve high-level pharma portfolio strategy or Roche organization structure and decision-making by drawing on case examples or other information from the external environment Actively identifying CI information, data collection, and insight communication to varied stakeholders Based on knowledge of impending strategic decisions, identify available data sources, collect competitive intelligence, and synthesize information for commercial, medical, and scientific leaders Manage external vendor relationships for collection and structuring of CI data including planning and execution of CI at medical scientific conferences
Basel Stadt | Freelance/Contracting project | hays-searchresults-startdate | 424898/1
Assume the Medical Affairs (MA) strategic lead for medical team(s) dedicated to special therapeutic area(s),this includes leading people and providing strategic guidance, as well collaboration with Life Cycle Leaders and other stakeholders in a matrix organisation for producing and execution of the medical strategy for the therapeutic area Responsible for appropriate resource planning in the teams to guarantee activities take place as planned, and within budget Responsible for delivery and maintenance of strategically aligned medical plans within therapeutic area (oncology, lung cancer experience Responsible for people management and development, as well as all other line manager responsibilities Personally responsible for acting in line with legal, regulatory and company standards and codes of practice
Basel Stadt | Freelance/temporary employment for a project | hays-searchresults-startdate | 420869/1
Ensure the development/transfer and validation of specific and sensitive bioanalytical methods required for the drug candidates and any concomitant/ interaction therapies in a given project working closely with the internal labs and external providers (CROs Manage and direct analysis of samples and timelines from non-clinical and clinical studies for the project at CRO labs Participate actively in DMPK, clinical and study management sub-teams Review protocols and guide project teams in all aspects of bioanalytical work required for the project Review data and reports for regulatory submissions. Support filings and answer any questions coming from the regulatory agencies, as applicable Ensure full compliance with the current global and local bioanalytical regulatory guidance Ensure that the most advanced and most efficient procedures are used at the CRO Remain current and continually develop expertise in bioanalytical sciences of small molecules, including oligonucleotides analysis
Basel Stadt | Freelance/Contracting project | hays-searchresults-startdate | 420216/1
As a member of the Category Management team you are responsible for proactively identifying opportunities, engaging, and partnering with Business stakeholders and regional Procurement, and managing Category suppliers to deliver overall Category performance and saving targets. Support the definition of Category Strategy and Annual Pipeline for the Category of External Manufacturing Services on either a global or regional basis: Collate supplier, market, category and internal data and Business requirements to formulate and validate the Category Strategy and develop a pipeline of proactive initiatives based on the Category Strategy, local requirements and stakeholder planning activities. You have deep category subject matter knowledge and expertise in the supplier management approach, the specific assigned categories and work to ensure this knowledge is shared and embedded to drive performance. You provide deep expertise in supporting the realization of Procurement targets, including delivery of high value sourcing, demand management, process re-engineering, and supplier performance and innovation activities. Develop category buying guides and content to translate the Category Strategy and outcomes into clear guidance and executable content. CMO As a CMO subject matter expert and key user you are a member of the direct procurement team within the future ERP program. You will act as a liaison between Business Process Management, Direct Procurement and the ERP program workstream. The role supports the project team in analyzing business operations to assist in the design/redesign and documentation of business processes and clear definition of the business requirements regarding processes for the CMO Business Scenario (Supplier Management, Requisition to Pay, etc.). You work with operational teams, key users and other stakeholders to ensure understanding and alignment of reporting needs and E2E data governance processes. Compliance with all policies and procedures on a global and local level is an essential part of the design considerations. You implements process improvements through the introduction of appropriate workflows, tools and approval processes as well as though harmonization of processes and system design in close alignment with technical operations and finance. The design activities include translation of detailed business requirements to IT and management of changes to design specifications.
Marburg | Freelance/Contracting project | hays-searchresults-startdate | 407870/1
Erect a new production building as a green field project Cover all engineering disciplines within an ECPM approach with external engineering office (EO) Ensure implementation of the GSK standards and requirements with a team of GSK engineers as counterpart to EO engineers Check engineering documents on design aspects Monitor process of Clean Utilities engineering, review, rework and approval of documents Key project responsible for Clean Utilities Alignment with Global Engineering standards
Basel Stadt | Freelance/temporary employment for a project | hays-searchresults-startdate | 408485/11
Identify evidence needs and recommend data solutions: ask the right scientific questions, understand the evidence needs for research and development, regulatory and market access, and ideate and make recommendations on fit-for-purpose data and analytics solutions Drive into data: develop a comprehensive and deep understanding of the data we work with using analytical tools and applications to broaden data accessibility and advance our proficiency/efficiency in understanding and using the data appropriately Be an expert in applying methods: stay current with and adopt emergent analytical methodologies, tools and applications to ensure fit-for-purpose and impactful approaches Produce high quality analyses: apply rigor in study design and analytical methods; plan for data processing; design a fit-for-purpose analysis plan, assess effective ways of presenting and delivering the results to maximize impact and interpretability; implement and/or oversee the study, including its reporting; ensure compliance with applicable pharma industry regulations and standards Interpret and share results: communicate findings to internal stakeholders, regulatory, health technology assessment (HTA) bodies and scientific communities; publish results; participate in external
Lower Austria | Freelance/Contracting project | hays-searchresults-startdate | 392752/6
End to end project from design through construction to C&Q Interface with the design team, equipment vendors, construction team and C&Q experts Develop project plans and strategies and successfully execute them according to established schedule, cost and performance standards (biotech)

hays-searchresults-links-headline