Gehaltsübersicht für Contract Manager in Basel-Stadt

 Perfect Candidate:The perfect candidate is someone with a scientific background and 5-8 years of experience in a similar position. This person should have strong experience with alliance and project management: driving projects with external partners (government and funding initiatives). We are looking for someone with experience in industry (pharma and/or biotech). We need someone with excellent stakeholder management and communication skills to drive projects, be an advocate for the project put forward to the external partner negotiate for funds. Tasks & Responsibilities:Management of the relationship with the partner to ensure partnership progress and resolution of key challengesCreates, prepares and manages integrated master project plans and revises them as neededFacilitates and coordinates project setup, planning, implementation and progressManages project deliverables, costs, work schedules, scope and resource requirements throughout the projectsFulfils all reporting requirements in alignment and compliance with contractual obligations, managing all issue and conflict actively to the benefit of the partnershipManages the preparation of reports to document project progress, financial status and ensures project documents are complete, current, and stored appropriatelyMotivates project team for the delivery of all contract related project deliverablesImplements contractual amendments in coordination with Legal, Finance and all relevant internal stakeholdersSingle point of contact to collect project-related data from various team functions to compile reports. Tactical coordination of timelines/budgets for all projects and functions within an areaDelivers informative, well-organized reports and presentations on project status and selected project topicsMonitor and report on project issues, risks, changes, progress and deviations from plan and escalate to functional management in a timely fashion and propose mitigation strategiesDrives project management excellence through best-in-class project management methodologies, systems and tools. Set-up and adapt relevant project management processes and structure in alignment with stakeholders and ensure process implementation within project teamEffectively facilitates and leads project team meetings (set agenda, organize meetings, edit minutes). Participates as a member of the project team. Holds regular status meetings with project team to ensure milestones are being metPrepares and leads joint governance committee meetings working with internal and external senior leadershipConducts post-project debrief to identify and communicate learnt lessonsCollaborates to establish a working relationship with Pharma and Diagnostics development and supporting functions. Works within global cross-functional teams to build strong business relationshipsEffectively manages communications, expectations, and interactions with all departments and internal and external stakeholders. Identify and assess impact on all stakeholders and manage the communication accordingly Requirements:Minimum Bachelor’s Degree in Life Science or Healthcare Minimum 5 years of experience in relevant similar role Scientific background and sound knowledge of drug development from early discovery to end of life cycle (pharma or biotech experience) Extensive alliance or project management experience, preferably in pharmaceutical product development or other healthcare-related field Experience with project management disciplines, methodology, tools and project management reporting elements for projects funded by external grants and contracts Excellent stakeholder management (C-level) and ability to effectively collaborate across global organizations, build consensus, and manage conflict in challenging or difficult situationsStrong experience in the preparation of master project plans and the preparation of complex project reportsOutstanding strategic and operational management skills with the ability to develop and present sound proposals and recommendations with high-qualityAbility to successfully manage multiple projects simultaneouslyExceptional organizational & time management skills: proven ability to manage complex objectives and goals to an effective and efficient conclusionExcellent interpersonal and communication skills with a proven ability to lead and develop project teams of diverse expertise on both a direct and matrix basis to achieve organisational objectivesAble to work effectively across culturesStrong oral and written communication skills, including fluency in written and verbal English Nice to haves:Advanced degree (PhD, MBA and/or MD)Experience in managing projects funded by government grants such as BARDA contractsExperience in the infectious diseases healthcare landscape 

The perfect candidate is someone who has done a similar position in bioanalysis previously within a pharma (preferred) or a CRO or an experienced scientist with experience with small and/or large molecules very keen to learn and with a positive attitude. Please note the preference goes to the first profile (experience in pharma/CRO). In any case, the successful candidate will have an education within biology / biochemistry. On this position, the perfect candidate has strong experience on both small AND large molecules. This is a long-term contract with a potential internal opportunity afterwards.  Tasks & Responsibilities:Lead bioanalytical strategies to generate decision-enabling bioanalytical data with skilled data interpretation to meet and answer project needsResponsible for outsourcing activities in Bioanalytics (bioanalysis of non-clinical and clinical studies); resource and time planning, coordination and administrative management of studies with CROs.Manage the development, transfer and validation of specific and sensitive bioanalytical methods required for the development compound (drug), anti-drug antibodies (ADA), soluble targets and any concomitant/interaction compound in the given project.Manage and direct analysis of samples and timeline from preclinical and clinical studies for the project at CRO labs.Participate actively in PS subteams, act as primary contact person for DMPK project leader.Act as Bioanalytical Leader when required. Interact proactively with the assay development team.Ensure full compliance with the current global and local bioanalytical guidance and GxPs.Leadership in Bioanalysis: *remain current and continually develop expertise in bioanalytical science. Contribute to scientific consortia when required; *maintain current expertise in the validation and conduct of bioanalytical assays; *guide and manage the bioanalysis at CROs and ensure that most advanced and most efficient procedures are used.Provide technical leadership in issue resolution.Review protocols and other relevant documents and guide project teams in all aspects of bioanalytical work required for the project.Review and write reports for regulatory submissions; support filings and answer any questions about bioanalytics coming from the regulatory agencies.Maintain open links with other disciplines within the department and the organization.Advise Group Head concerning all needs relating to administrative processes, technologies and equipment. Inform him of all critical issues Must haves:Minimum 3 years in a similar position focused on bioanalysis in pharma or CRO (pharma preferred) OR scientist focused on bioanalysis Excellent work experience on both large and small molecules bioanalysis Strong vendor management experience, looking after outsourced studies to external CROsDegree in biology/biochemistry  

Our People & Places Solutions business – reinforces our drive to improve the lives of people everywhere and epitomizes the "why" of what we do – the tremendous positive impact and value our solutions bring to our communities and society as a whole. From facilities delivering life-saving therapies and ensuring clean water to enabling the connection of people through all modes of transportation and providing access to technology – we're integrating a multitude of these solution elements to build the smart environments of tomorrow.Start your Jacobs career with a company that inspires and empowers you to deliver your best work so you can evolve, grow and succeed – today and into tomorrow.Your Impact:Our office in Basel has a strong focus on life science industries mainly serving pharmaceutical and biotechnology companies.Our contribution ranges from early feasibility studies to modifications of existing facilities and production lines up to the realization of large green field projects.Key Role Responsibilities: Verwaltung von Aktivitäten im Zusammenhang mit Verträgen für Dienstleistungen, den Kauf von Equipment, Materialien oder Produkten Ansprechpartner*in für Kunden und Unterauftragnehmer Prüfung von Kostenvoranschlägen für Material, Ausrüstungsleistungen, Produktionskosten, Leistungsanforderungen und Lieferplänen, um deren Richtigkeit und Vollständigkeit sicherzustellen Durchführung von Vertragsänderungen, Datenverwaltung und Koordinierung mit Unterauftragnehmern Unterstützt bei der Erstellung und Bearbeitung von Mehraufwänden Verfolgt die Mehraufwände mit den Mitgliedern des Projektteams, um sicherzustellen, dass sie den Genehmigungsprozess rechtzeitig und korrekt durchlaufen Unterstützung im Bereich Quantity Surveying Zusammenstellung von Daten zur Erstellung von Statusberichten für Auftragnehmer zur Unterstützung des Änderungsmanagements, des Zahlungsmanagements und des Kostenmanagements von Verträgen Erstellung von Berichten und Unterstützung des Cost Manager bei seinen täglichen Aktivitäten Here’s What You’ll Need: Abgeschlossenes Hochschulstudium (oder vergleichbar), vorzugsweise im Bereich Business Administration Mindestens 5 Jahre Erfahrung im Bereich der Auftragsvergabe, vorzugsweise bei bedeutenden pharmazeutischen oder biotechnologischen Projekten Englische sowie Deutsche oder Französische Sprachkenntnisse sind ein Muss. Weitere Sprachkenntnisse sind ein Plus. Ausgeprägte Kommunikationsfähigkeiten Ethisches Verhalten, angemessener Umgang mit vertraulichen Daten, Zuverlässigkeit Hohes Bewusstsein für Arbeitssicherheit und Gesundheitsschutz Bereitschaft zu Reisetätigkeit in der Schweiz und Europa Was wir Dir bieten: Aktive Mitarbeit bei der Etablierung unserer Schweizer Niederlassung Eigenverantwortung und Handlungsspielraum Karrieremöglichkeiten in einem internationalen Unternehmen Gute Sozialleistungen At Jacobs, we’re challenging today to reinvent tomorrow by solving the world’s most critical problems for thriving cities, resilient environments, mission-critical outcomes, operational advancement, scientific discovery and cutting-edge manufacturing, turning abstract ideas into realities that transform the world for good. With $13 billion in revenue and a talent force of more than 55,000, Jacobs provides a full spectrum of professional services including consulting, technical, scientific and project delivery for the government and private sector.Jacobs Basel Unbefristet Vollzeit 14 Stunden her

Category Manager (m/f/d) 100% CordenPharma is a leading full-service contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (APIs), excipients and pharmaceuticals Drug Products (DP) and packaging capabilities with > 2’600 employees across the world. Our services enable pharmaceutical and biotech companies to manufacture medicines with the ultimate goal of improving people’s lives. Our network in Europe and the US offers flexible and specialized solutions across five technology platforms: Peptides, Lipids & Carbohydrates; Injectables; Highly Potent & Oncology; and Small Molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the well-being of patients. At the earliest possible date we are looking for a Category Manager (m/f/d) 100%Basel, Switzerland Basel Q3 2024 Full-time Permanent Main activities and responsibilities CordenPharma is looking for experienced Category Managers who would like to join our talent pool for future projects in order to complete the Global Category Team in the following areas: CAPEX; MRO (Maintenance, Repairs/operations); Liquid Drug Product Packaging; Drug Product Excipients, Energy. In this role, you would be part of the future Global Procurement team supporting the business objectives in procurement of goods and services for the Corden Pharma group. You will represent your category across the individual Corden sites and, as such, build a crucial link between global and site Procurement. Responsible for developing and executing category strategies, conducting market analyses and research, managing relationships with key suppliers, and supporting contract negotiation and execution as required. Your primary objective is to secure the delivery of projects, goods and services across the category, thus effectively managing Corden’s Supply Chain risk. You will achieve the best value solutions for the Corden Pharma group through effective communication, and collaboration across internal departments, and by maintaining strong relationships with suppliers. Your Profile Degree or Business Administration Ability to lead cross-functional and global team Category Management experience in any of the areas; CAPEX; MRO (Maintenance, Repairs/operations); Liquid Drug Product Packaging; Drug Product Excipients, is a desired Commercial strategic sourcing experience (ideally with a multi-national, Fortune 500 business) including demonstrated proficiency in contract negotiations, supplier development, and global sourcing Professional Purchasing Qualification Strong external and internal communication skills Influencing, negotiation and project management skills Experience in the pharmaceutical (especially CDMO) or chemical industry Excellent knowledge of SAP Excellent computer-based skills, including proficiency in Microsoft Office Strong proficiency in Business English What we offer 30 days of vacation Dynamic and exciting work environment Retirement Pension Plan Flexible Working Hours Interested? Your contact person Brandt, Raphael

Senior Quality Partner - Produktqualitätsexperte für Medizinprodukte und IVDsUnternehmenseinblick:Möchten Sie Ihre Leidenschaft für Qualität und Regulierung in der Medizintechnikbranche ausleben?Im Operations Quality Netzwerk RDI/RDA suchen wir einen Senior Quality Partner, der die Produktqualität und -integrität von Medizinprodukten und In-vitro-Diagnostika (IVDs) auf ein neues Level hebt.Die Aufgabe:In dieser Schlüsselposition übernehmen Sie die Verantwoveröffentlicht am 7. September 2023Senior Quality Partner - Produktqualitätsexperte für Medizinprodukte und IVDsUnternehmenseinblick:Möchten Sie Ihre Leidenschaft für Qualität und Regulierung in der Medizintechnikbranche ausleben?Im Operations Quality Netzwerk RDI/RDA suchen wir einen Senior Quality Partner, der die Produktqualität und -integrität von Medizinprodukten und In-vitro-Diagnostika (IVDs) auf ein neues Level hebt.Die Aufgabe:In dieser Schlüsselposition übernehmen Sie die VerantwoKontaktDiogo MeloReferenznummer19923Beschleunige die Bewerbung, indem du dein Profil teilstJob DetailsDu hast ein abgeschlossenes naturwissenschaftliches oder technisches Studium. Besonderer Fokus liegt auf der praktischen Berufserfahrung als QA Specialist/QA Manager an einem Produktionsstandort in einem GMP regulierten Unternehmen. Du Bist ein Person verfügt über Routine in der Quality-Rolle bei der Bearbeitung von Abweichungen, Technischen Changes und CAPAs.Allgemeine Informationen:Startdatum: asapSpätestmögliches Startdatum: 01.04.2024Geplante Dauer der Anstellung: 31.12.2024 / MutterschaftsvertretungVerlängerung (bei Befristung): Abhängig von Dauer der MutterschaftsvertretungWorkload: 80-100%Home Office: max. 40%Aufgaben & Verantwortlichkeiten:- Fachliche Rolle:End-to-end Quality Oversight über die GMP-Compliance aller Anlagen & Systeme im zugewiesenen Zuständigkeitsbereich insbesondere in Bezug auf Commissioning & Qualification, CSV, Kalibrierung, Wartung und Data IntegriyQuality Review und Freigabe von GMP-Records aus den jeweiligen Quality Systems (SOPs, Risikoanalysen, Change Control, Abweichungen, Qualifizierungsdokumente, etc.)Quality Oversight als Teammitglied bei technischen Investitionsprojekten, bei Root Cause Analysen, bei technischen Risikoanalysen und VerbesserungsprojektenPräsentation von Themen bei Behördeninspektionen und internen Audits- Rolle in der Organisationsentwicklung:Proaktive Förderung des gegenseitigen Austauschs über die fünf Quality Abteilungen am Standort hinweg zur fachlichen und organisatorischen Weiterentwicklung der Quality UnitEngagierte Impulse zur Harmonisierung von Abläufen und zu “One Quality Voice”Must Haves:Abgeschlossenes Studium im Bereich Life Sciences oder einem technischen Bereich Min. 1-3 Jahre praktische Erfahrung als QA Specialist/QA Manager an einem Produktionsstandort in einem GMP regulierten Unternehmen Routine in der Quality-Rolle bei der Bearbeitung von Abweichungen, Technischen Changes und CAPAs Erfahrung mit der Qualifizierung und Inbetriebnahme neuer Produktionsanlagen ist von VorteilSehr gute Deutsch- und Englischkenntnisse in Wort und SchriftVersierter Umgang mit IT Office Applikationen (z.B. Google Drive) sowie mit gängigen IT Systemen im Pharmaumfeld (z.B. TrackWise, Veeva, SAP, Documentum, LIMS, etc).Wir bedanken Dir für Deine Bewerbung :)Du hast ein abgeschlossenes naturwissenschaftliches oder technisches Studium. Besonderer Fokus liegt auf der praktischen Berufserfahrung als QA Specialist/QA Manager an einem Produktionsstandort in einem GMP regulierten Unternehmen. Du Bist ein Person verfügt über Routine in der Quality-Rolle bei der Bearbeitung von Abweichungen, Technischen Changes und CAPAs.Allgemeine Informationen:Startdatum: asapSpätestmögliches Startdatum: 01.04.2024Geplante Dauer der Anstellung: 31.12.2024 / MutterschaftsvertretungVerlängerung (bei Befristung): Abhängig von Dauer der MutterschaftsvertretungWorkload: 80-100%Home Office: max. 40%Aufgaben & Verantwortlichkeiten:- Fachliche Rolle:End-to-end Quality Oversight über die GMP-Compliance aller Anlagen & Systeme im zugewiesenen Zuständigkeitsbereich insbesondere in Bezug auf Commissioning & Qualification, CSV, Kalibrierung, Wartung und Data IntegriyQuality Review und Freigabe von GMP-Records aus den jeweiligen Quality Systems (SOPs, Risikoanalysen, Change Control, Abweichungen, Qualifizierungsdokumente, etc.)Quality Oversight als Teammitglied bei technischen Investitionsprojekten, bei Root Cause Analysen, bei technischen Risikoanalysen und VerbesserungsprojektenPräsentation von Themen bei Behördeninspektionen und internen Audits- Rolle in der Organisationsentwicklung:Proaktive Förderung des gegenseitigen Austauschs über die fünf Quality Abteilungen am Standort hinweg zur fachlichen und organisatorischen Weiterentwicklung der Quality UnitEngagierte Impulse zur Harmonisierung von Abläufen und zu “One Quality Voice”Must Haves:Abgeschlossenes Studium im Bereich Life Sciences oder einem technischen Bereich Min. 1-3 Jahre praktische Erfahrung als QA Specialist/QA Manager an einem Produktionsstandort in einem GMP regulierten Unternehmen Routine in der Quality-Rolle bei der Bearbeitung von Abweichungen, Technischen Changes und CAPAs Erfahrung mit der Qualifizierung und Inbetriebnahme neuer Produktionsanlagen ist von VorteilSehr gute Deutsch- und Englischkenntnisse in Wort und SchriftVersierter Umgang mit IT Office Applikationen (z.B. Google Drive) sowie mit gängigen IT Systemen im Pharmaumfeld (z.B. TrackWise, Veeva, SAP, Documentum, LIMS, etc).Wir bedanken Dir für Deine Bewerbung :)kontaktiere uns.wir sind da um deine Fragen zu beantworten.DMDiogo Melo+41 58 201 56 62 Zürich Professionals ITder Bewerbungsprozess.Erfahre wie der Bewerbungsprozess aussieht. Finde heraus wie wir dir helfen werden, diesen Job zu bekommen.1 von 8mit randstad bewerben.Wir werden deine Bewerbung überprüfen und sehen, ob du zu diesem Job und Unternehmen passt.2 von 8Wir werden dich kontaktieren.Unser Consultant wird dich zu einer passenden Zeit anrufen und mit dir deine Bewerbung und deine Karriereziele besprechen. 3 von 8deine registrierung.Falls du noch nie mit uns zusammengearbeitet hast, brauchen wir ein paar Informationen um herauszufinden, ob du in der Schweiz arbeitsberechtigt bist.4 von 8background check.Um sicherzustellen, dass du der perfekte Kandidat für diese Rolle bist, werden wir alle relevanten, von dir zur Verfügung gestellten Referenzen kontaktieren.5 von 8der perfekte job für dich.Unser Expertenteam wird entweder ein Vorstellungsgespräch für die Stelle arrangieren, auf die du dich beworben hast oder passende alternativen vorschlagen.6 von 8das interview.Wir werden sicherstellen, dass du vollständig für dein Interview vorbereitet bist und weisst, was dich erwartet. Viel Glück!7 von 8dein start im neuen job.Gratulation! Du bist bereit für deinen neuen Job. Unser Team wird sicherstellen, dass du vollständig vorbereitet für deinen ersten Arbeitstag bist.8 von 8beginne deinen neuen job.Nachdem du deine neue Herausforderung begonnen hast, werden wir dich kontaktieren und sehen, wie es dir geht und wie wir dich in deiner neuen Rolle unterstützen können.ähnliche jobs.Basel, Basel-StadtContractThe roles within IMP Quality Operations Switzerland Clinical Packaging Team require a high level of flexibility, ability to work under pressure and sense of responsibility.You are inspiring, self-reflected and creative on the one hand and are clear in communication as well as integrative in solution processes on the other. General Information:Start date: asapLatest Start Date: Hiring manager considers candidates with a notice period of max. 3 monthsEnd datveröffentlicht am 16. Januar 2024The roles within IMP Quality Operations Switzerland Clinical Packaging Team require a high level of flexibility, ability to work under pressure and sense of responsibility.You are inspiring, self-reflected and creative on the one hand and are clear in communication as well as integrative in solution processes on the other. General Information:Start date: asapLatest Start Date: Hiring manager considers candidates with a notice period of max. 3 monthsEnd datBasel, Basel-StadtContract

Project Manager Construction & Facility Management (fixed term 18 months) Since 1967, Jet Aviation has been crafting flight in its smoothest form. From one hangar in Basel, Switzerland, to some 4,000 employees, and some 50 locations worldwide. Aircraft Management, Aircraft Sales, Charter, Completions, Defence, FBO, Fixed and Rotary Wing Maintenance, and Staffing. Behind every seamless Jet Aviation experience, is a team of dedicated professionals perfecting the art of flight. The artisans of aviation. The craft that brings our customers’ journey to life. In the hangar, on the ground, and behind the scenes. Enabling global flight, with passion. Position Summary In this position you will be responsible to successfully manage and coordinate facility projects and activities in a key role in the Real Estate & Facility Management department. Main Responsibilities Direct and coordinate Facility and Infrastructure projects including, but not limited to, construction, repairs, refurbishments, or new installations Manage complex projects, planning, reporting, KPI’s through Capex plan Provide high quality customer service and functional support to all internal customers Responsible for the coordination and execution of tasks carried out by external suppliers Ensure the proper functioning of facilities and building operations through Maintenance & Services by coordination with Airport, suppliers, and contractors Manage Facility Construction & Maintenance contracts and oversee contract renewals, modifications, and obligations Review and evaluate performance of suppliers and contractors to ensure value for money and efficient operating costs Respond appropriately to emergencies or urgent issues as they arise Minimum Requirements Bachelor’s Degree and 5 years of experience in a Project Management role in Real Estate Very good computer skills, AutoCAD and Microsoft Office and Microsoft Project would be an advantage Very good oral, written and communication skills and the ability to successfully interact with internal and external stakeholders at all levels Fluent in English and French, German would also be an advantage Able to respond to sensitive issues, high accountability, excellent customer-service and hands-on mentality skills If you are interested in a multicultural, challenging and innovative working environment and your profile matches our requirements, we are looking forward to receiving your online application in English.

Für unsere Niederlassung in Basel suchen wir Sie für das Gebiet Basel - Bern als Field Sales Manager (w/m/d).Ihre Aufgaben:... Read moreAkquisition von Neukunden, Ermittlung von Potentialen, Förderung der Geschäftsausweitung im Sales Gebiet Basel - Bern Persönliche sowie virtuelle Präsentation und Vermarktung aller DB Schenker Produkte und Dienstleistungen Eigenverantwortliche Bearbeitung der zugewiesenen Region, strategischer Ausbau des Kundenportfolios Schnittstellenkoordination zu internen Fachabteilungen, Mitarbeit bei Sales-Aktionen, Messen und Events Aktive Wettbewerbs- und Marktbeobachtung Kundendatenpflege in der firmeneigenen Software QualificationsIhr Profil:Kaufmännische Ausbildung/ Studium, idealerweise im Bereich Spedition, Logistik Berufserfahrung im Sales, Fachkenntnisse in der Logistik wünschenswert Spaß an der Arbeit mit Kunden, lösungsorientiertes Vorgehen, Überzeugungskraft, diplomatisches Geschick, Empathie und ausgeprägte Abschlusssicherheit Sicheres, verbindliches und seriöses Auftreten, kommunikative Fähigkeiten Gute Englischkenntnisse in Wort und Schrift, Erfahrung mit MS Office-Paketen, Fahrausweis sowie bei Bedarf Reisetätigkeit im Gebiet Wir bieten:... Read moreFlache Hierarchien und kurze Entscheidungswege mit Freiraum und Eigenverantwortung Ein hochmotiviertes und top aufgestelltes Team Fortschrittliche Anstellungsbedingungen und Sozialleistungen 27 Tage Ferien sowie attraktive Benefits und Weiterbildungsmöglichkeiten Kostenlose Mitarbeiterparkplätze Möglichkeit für teilweise Homeoffice Tätigkeiten Field Sales Manager (w/m/d)Do you have any questions?We are happy to helpFeel free to reach out to our recruiters if you need more information about this positionHolger PeplauTalent Acquisition [email protected] Your ApplicationPositionField Sales Manager (w/m/d)CompanyDB SchenkerLocationBasel, Basel, Bern, SwitzerlandJob GroupAir Freight, Contract Logistics/Supply Chain Mgmt, Land Transport/Trucking, Ocean Freight, Sales/Key Account ManagementType of ContractFull TimeRef #309979Wenn Sie an dieser abwechslungsreichen Aufgabe interessiert sind und ein engagiertes Team verstärken und unterstützen möchten, dann freuen wir uns auf Ihre Bewerbung, unter Angabe des möglichen Eintrittszeitpunktes und Ihrer Gehaltsvorstellung.Bitte bewerben Sie sich einfach direkt über unser Bewerberportal. Laden Sie dort Ihren Lebenslauf, Anschreiben und Zeugnisse (idealerweise als .pdf) hoch.Bei Fragen nehmen Sie gerne Kontakt mit uns auf:Schenker Schweiz AGHerr Holger PeplauTalent Acquisition [email protected] DB Schenker sind wir stolz auf die Vielfältigkeit unserer Teams und entschlossen, diese weiter voran zu treiben. Daher heißen wir alle Bewerber willkommen, unabhängig von Geschlecht, Alter, Behinderung, Nationalität, Religion oder sexueller Orientierung.DB Schenker akzeptiert keine Bewerbungen von Agenturen. Bitte leiten Sie keine Lebensläufe an unsere Bewerbungspostfächer, Mitarbeiter oder Unternehmensstandorte weiter. Schenker Deutschland AG/DB Schenker übernimmt keine Haftung für Kosten, die sich im Rahmen unaufgeforderter Bewerbungen ergeben.DB Fernverkehr AGVeröffentlicht:03 Februar 2024Pensum:100%Vertrag:FestanstellungArbeitsort:BaselField Sales Manager (w/m/d)Field Sales Manager (w/m/d)IntroductionBei DB Schenker sind Sie Teil eines globalen Logistiknetzwerks, das die Welt verbindet. Ein Netzwerk, das es Ihnen ermöglicht, Ihre Karriere aktiv mitzugestalten und Sie dazu anspornt neue Wege zu gehen. Mit mehr als 78.000 Kolleginnen und Kollegen weltweit heißen wir Vielfalt willkommen und wachsen mit den Erfahrungen, Perspektiven und Fähigkeiten jedes Einzelnen. Gemeinsam sind wir hier, um zu bewegen. ... Read moreResponsibilities

Facility Manager EMEA Workplace Services Since 1967, Jet Aviation has been crafting flight in its smoothest form. From one hangar in Basel, Switzerland, to some 4,000 employees, and some 50 locations worldwide. Aircraft Management, Aircraft Sales, Charter, Completions, Defence, FBO, Fixed and Rotary Wing Maintenance, and Staffing. Behind every seamless Jet Aviation experience, is a team of dedicated professionals perfecting the art of flight. The artisans of aviation. The craft that brings our customers’ journey to life. In the hangar, on the ground, and behind the scenes. Enabling global flight, with passion. Position Summary As Facility Manager EMEA Workplace Services of Jet Aviation, you will manage workplace and services to ensure the organization’s facilities is in an optimal, and high-quality work environment. In this role you will be collaborating closely with the VP Real Estate & Logistics EMEA and serve as a liaison between leadership, employees, operations, and external contractors called in support of the Facilities Department. Main Responsibilities Manage and follow-up Basel Facility Services and workplace management activities Oversee and support when required EMEA Facility Services and workplace management activities Coordinate, develop, optimize all assigned services and overseeing all ticketing activities Ensure at any point of time maximum customer satisfaction and high quality of service Respond to and follow-up on all requests in a timely and efficient manner including providing guidance to resolve day-to-day facility related issues Proactively address service issues, complaints/escalations, or incidents including tracking action plan to closure Coordinate, develop, optimize space policy and the Basel Facility Master Plan Manage daily space requests and coordinate inter-office moves, propose alterations, challenge requests, track progress and ensure timely completion Manage supplier relationships including service contracts with vendors, regular and ongoing performance & budget monitoring (KPIs, SLAs), quarterly business reviews, financial review, conducting RFPs, and ensure contract fulfilment Develop an annual operating budget, identify cost-savings opportunities and review expenses on a monthly basis Support leadership and companies’ event Ensure operator’s responsibility and employer obligations with regards to occupational health and safety in accordance with applicable laws and guidelines, as well as minimizing possible risks Minimum Requirements Minimum Bachelor's degree and ideally 8-10 years of experience in Facility Management, Workplace Experience, Hospitality or similar roles Excellent customer-service focused attitude and ability to respond to sensitive issues and handle multiple priorities, Strong written/oral communication and presentation skills, ability to successfully interact with internal and external stakeholders at all levels Excellent organizational and communication skills Capability to diagnose, handle and resolve issues quickly and efficiently, including experience prioritizing and assigning materials and resources Attention to detail and great follow-up skills essential as well as project management experience Results driven – able to execute with high personal accountability and organizational skills Strong computer skills including solid understanding of Microsoft Office Fluent in English and French, German would be a plus Strong personal values corresponding with Jet Aviation values (Trust, Honesty, Alignment, Transparency) If you are interested in a multicultural, challenging and innovative working environment and your profile matches our requirements, we are looking forward to receiving your online application in English.

Category Manager (m/f/d) 100% CordenPharma is one of the leading Contract Development and Manufacturing Organizations (CDMO) and develops and produces active pharmaceutical ingredients, medicines and associated packaging services on behalf of its customers as a “full-service” service provider. The group employs around 3,000 people. Our network in Europe and the USA offers flexible and specialized solutions across five technology platforms: peptides, lipids & carbohydrates, injectables, highly potent active ingredients & oncology and small molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the benefit of patients. CordenPharma International (CPI) acts as the management company of the CordenPharma Group. In addition to the Executive Leadership Team, CPI has central functions such as Sales & Marketing, Legal, HR and Corporate Development, which work for the CordenPharma Group across locations and at an international level. We are looking for one as soon as possible Category Manager (m/f/d) 100%Basel, Switzerland Basel Q3 2024 Full-time Permanent Main activities and responsibilities CordenPharma is looking for experienced Category Managers who would like to join our talent pool for future projects in order to complete the Global Category Team in the following areas: CAPEX; MRO (Maintenance, Repairs/operations); Liquid Drug Product Packaging; Drug Product Excipients, Energy. In this role, you would be part of the future Global Procurement team supporting the business objectives in procurement of goods and services for the Corden Pharma group. You will represent your category across the individual Corden sites and, as such, build a crucial link between global and site Procurement. Responsible for developing and executing category strategies, conducting market analyses and research, managing relationships with key suppliers, and supporting contract negotiation and execution as required. Your primary objective is to secure the delivery of projects, goods and services across the category, thus effectively managing Corden’s Supply Chain risk. You will achieve the best value solutions for the Corden Pharma group through effective communication, and collaboration across internal departments, and by maintaining strong relationships with suppliers. Your Profile Degree or Business Administration Ability to lead cross-functional and global team Category Management experience in any of the areas; CAPEX; MRO (Maintenance, Repairs/operations); Liquid Drug Product Packaging; Drug Product Excipients, is a desired Commercial strategic sourcing experience (ideally with a multi-national, Fortune 500 business) including demonstrated proficiency in contract negotiations, supplier development, and global sourcing Professional Purchasing Qualification Strong external and internal communication skills Influencing, negotiation and project management skills Experience in the pharmaceutical (especially CDMO) or chemical industry Excellent knowledge of SAP Excellent computer-based skills, including proficiency in Microsoft Office Strong proficiency in Business English What we offer 30 days of vacation Dynamic and exciting work environment Retirement Pension Plan Flexible Working Hours Interested? Your contact person Brandt, Raphael

Operation / Project Manager CMO - 100% Operation / Project Manager CMO Temporary employment, 100% Background We are looking for someone who would like to support our client, a biotechnology company in Basel, in their operational activities in collaboration with a CMO over the next 9 - 12 months. Tasks & Responsibilities Track the production, testing, release, and shipping plan at the CMO as per agreed MPS Coordinate review and approval of various CMO-related documents (e.g. deviations) as required to ensure the timely shipping and release on the manufactured batches Issue resolution/escalation of any unplanned event that needs cross-functional coordination Organize and lead cross-functional project teams, setting up governance meetings, agenda and meeting minutes. Prepare project milestone plan. Continue monitor execution versus plan. Follow up and prepare weekly/monthly reports updates Assist the Contract Management Process with CMOs and external partners. Execute contract terms including issuance of purchase orders, forecasts, and other deliveries. Track end-to-end status offers including review and approval process, contract execution, purchase requisition, invoices and final close out Profile University degree in Natural Sciences is desired Minimum 5 years of experience in Pharmaceutical/Biotechnology Industry and GMP environment Experience in working with CMOs Solid knowledge and expertise in Project Management Fluent in English, knowledge of Spanish is an advantage Open for temporary travelling to Spain General information Start date: asap Planned duration of employment: 9 - 12 months Workplace: Basel (3 days onsite, 2 days home office) Travel activities: to Spain for a few days every two months Workload: 100% Your application If you are interested, please send your CV in English to:nicole.blum[at]kellyservices.ch If you have any questions in advance, you can also contact Nicole Blum by phone on:+41 (0)61 270 80 14 or +41 (0)79 204 36 85 We look forward to hearing from you.Kelly Services SwitzerlandNicole Blum