Stellen in basel

On behalf of our client, an International Biopharmaceutical company, Swisslinx is looking for dedicated Accounting Professional to join their team in Basel. This is a great opportunity to bring your proven knowledge and expertise to an organization that offers a dynamic working environment. Your mission - Carry out all accounting responsibilities for the Swiss entities. - Prepare accurate and timely financial statements in accordance with policies - Perform monthly, quarterly and yearly financial closings and account reconciliations - Liaise on daily basis with internal departments and external suppliers to ensure effectiveness - Assist in regulatory reporting and additional ad-hoc tasks as required Your background - 5-8 years of experience in Accounting in an international environment - Relevant educational background (finance/accounting) - Accuracy and attention to details - Strong familiarity with US/local GAAP and SAP/4HANA - Solid communication and hands-on mentality - Fluent in English and German Candidates must have a valid Swiss or European permit or work rights to be considered for this position. If you would like to be considered for the role, please apply directly or send your CV to . We look forward you receiving your application! By applying for this position, I consent to the Swisslinx Group of companies: - storing my personal information (including name, contact details, Identification and CV information etc.) on their internal or external servers for the purpose of informing me of potential employment opportunities - using my personal information or - supplying it to third parties upon express consent for the purpose of informing me of potential job opportunities - transferring where applicable my personal information to a country outside the EEA/EFTA I also hereby agree to the Swisslinx privacy policy () and Terms of Use ()

Weekly and ad hoc meetings with the global BeiGene PV management team and safety CRO Review feedback and performance metrics relating to the safety CRO for proactive identification and management of potential safety issues Collaborate with PV Training & Compliance team, safety CRO and also clinical study CROs, as applicable, in the investigation of reasons for any late safety report(s) and assist in the finalization of corrective action & preventive action (CAPA) plans in a timely manner Ensures ongoing tracking of cases processed and/or submitted by safety CRO in order to ensure CRO is meeting specific drug safety data and quality targets for case handling and/or global submissions. Ensures safety CRO is compliant with all global reporting requirements to business partners, ethics committees and global regulatory authorities. Serves as the lead Drug Safety representative for various cross-functional clinical study teams, with a particular focus on studies managed by European Clinical Operations & or Medical Affairs team Participates in training investigators on SAE reporting obligations at European study kick off meetings Assists Drug Safety Operations leadership team with establishment and ongoing review of Key Performance Indicators (KPIs) for the safety CRO and applicable European business partners and/or vendors Participates in the review and approval of program-specific Safety Management Plans Oversees individual team activities as it relates to global SAE case management and global submissions activities. Collaborates closely with Drug Safety Operations Leadership team, EU QPPV, & Medical Safety team to develop global Drug Safety SOPs Responsible for timeline management and ensuring global submission of aggregate safety reports and line listings such as DSURs and other aggregate safety reports (e.g.; PSURs/PBRERs) as required Oversees SAE reconciliation activities on a regular basis, and ensures that safety CRO is processing and reconciling SAEs across BeiGene European-based clinical trials as per study timelines and per contract Manages communication and timelines with applicable partner companies, collaborative sponsors and respective CROs regarding the intake, case processing, medical review and global submission of ICSRs as well as global safety aggregate reports (expedited reports, DSURs, CIOMS II line listings) Liaises with regional head of EU Pharmacovigilance, various internal and external groups (e.g.; Clinical Operations, Data Management, Regulatory, QA) to maintain a high level of quality and consistency across functional teams on best practices and industry standards. Maintains currency with evolving international guidance and regulations for global safety reporting, safety surveillance and risk management in both a clinical and post-marketed setting (with a particular focus on EU Clinical Trial requirements for PV, as well as EU GVP Modules) May provide back up support for other Drug Safety Operations Managers as well as Head of Drug Safety Operations Actively participates and supports in PV global inspection readiness activities or regulatory inspection requests or interviews as needed Able to adjust to multiple demands and shifting priorities and react constructively in a high-energy, fast paced environment Excellent interpersonal and communication skills, both written and oral Excellent computer skills in Microsoft environment (Microsoft Excel, Power Point, SharePoint and Word). Strong experience with electronic data capture (EDC) and knowledge of clinical trial data management principles Argus Safety database and data entry and global submissions expertise required Understands safety database structures and is familiar with data retrieval tools, and coding dictionaries such as MedDRA, WHODrug). Experience developing and revising Drug Safety/PV SOPs Understanding of medical terminology and the ability to summarize medical information required Demonstrates initiative, teamwork and accountability A demonstrated ability to manage own workload, prioritize, plan and organize assignments and work under strict timelines is required. Self-motivated and capable of working independently The ability to provide direction to a team, and to influence peers and team members Ability to attend and effectively represent Drug Safety Operations on multidisciplinary teams and across global teams with membership in Europe, US, Asia/Pacific regions; ability to evaluate and analyze procedural gaps An excellent global pharmacovigilance knowledge base. Excellent project management skills with the ability to align internal and external resources

Die Firma agiert in der Beratung. Fachliche Gesamtverantwortung für alle von Digital & Innovation gesteuerten digitalen Zugangspunkte Entwickelt in enger Zusammenarbeit mit den Business-Units die Gestaltung der digitalen Kundenerlebnisse und koordiniert deren Umsetzung mit internen und externen Partnern Mitarbeit im Rahmen des Digital & ICT Boards bei der Entwicklung der MCH-Group im Rahmen von strategischer Arbeit und themenübergreifenden Initiativen Verantwortet die fachliche und organisatorische Entwicklung der digitalen Touchpoints der MCH Trägt die Budget- und Personalverantwortung von Digital Touchpoints & Services und stellt den wirtschaftlichen Mitteleinsatz sowie die Einhaltung der Governance sicher Hochschulabschluss idealerweise in Marketing oder Wirtschaftsinformatik Min. 10 Jahre Erfahrung im Management von digitalen Touchpoint in einem grösseren Unternehmen davon min. 5 Jahre Führungserfahrung (vorzugsweise mehrstufig) zwingend Erfahrung und erfolgreicher Track-Record bei der kundenzentrierten und agilen Entwicklung von digitalen Kanälen und Dienstleistungen Aktuelles Know-how in Online Marketing und wertschöpfendem Einsatz von CRM Profundes Verständnis der technischen Grundlagen von digitalen Kanälen und digitalem Marketing Vernetztes Denken in grösseren strategischen Zusammenhängen Kommunikatives und politisches Geschick Überzeugendes und sicheres Auftreten bei Gremien Sehr gute Sprachkenntnisse in Deutsch und Englisch

The company is a Bank. Provide technical leadership and product management expertise for the SharePoint platform Provide leadership in agile processes and rituals; mediates team discussions Analyse business requirements, extract technological needs from users' requirements and translates them into workable product backlog items Ensure that the design meets business requirements and that stakeholders understand the benefits, drawbacks, risks, costs and time scales of design decisions Provide production support for SharePoint Co-ownership of Microsoft Azure DevOps Server 2019, responsible for product management, support and enhancements Manages small projects and coordinates activities with team and stakeholders At least five years' experience in designing and implementing large scale SharePoint installations Ideally a Microsoft professional certification on SharePoint 2016 and/or 2019 Experience with SharePoint 2019 and SharePoint application model is an asset Strong hands-on experience with several of the following technologies: C#, Web API, TypeScript, Javascript, SQL Server Solid knowledge of design and integration patterns Solid knowledge of multi-tier architectures and microservices In depth understanding of best practices and tooling for CI/CD pipelines, Azure DevOps 2019, automated testing, code quality and package management Experience with SharePoint 2019 upgrade projects, including gap analysis and migration and testing strategies Experience using SharePoint as Records Management solution or integrating SharePoint with Records Management solutions is considered an asset Experience with automation testing, including frameworks, approaches and techniques Experience with secure software development lifecycle Very good communication skills; ability to establish strong working relationships with business areas and infrastructure teams Ability to take the initiative and organise own work; flexibility; service orientation; ability to perform under pressure against tight deadlines Good problem solving and root cause analysis approach Ability to formally document and communicate complex system specifications

The company is a consulting firm. Lead efforts to improve and align Accounts Receivable global outcomes Review and implement standardized policies and process over collections, dispute management and credit. Collaborate and influence order management. Drive strategic improvements in cash flow and DSO (daily sales outstanding) Recommend and Implement Key Performance Indicators Develop insightful analytics and metrics to drive performance Lead successful implementation of process improvements and software Partner with major Invoicing Automation initiative across the company Drive culture of continuous improvement and accountability across the Clinical Trials Division Strong Business Acumen Change management skills Ability to attract and retain talented team; create proactive training and development plans Travel requirements 20 - 40% The ideal candidate will exhibit leadership, initiative, and the Thermo Fisher Scientific 4-I values of Integrity, Intensity, Innovation, and Involvement  Bachelor's Degree is required; focus on Accounting / Finance Minimum 10+ Years finance experience with increasing responsibility; pharmaceutical experience preferred Project Management Leadership (successfully led projects) Strong Analytical capabilities Multi-national environment Business to Business Collections in healthcare industry Excellent collaboration and communication skills Requires critical thinking and problem solving skills Goal Oriented, self-starter and proactive business partner Excellent interpersonal and communication skills with the ability to build relationships in a matrix environment as well as influence employees Strong Microsoft Excel and systems skills

The firm is a leading agriculture company. Work with business stakeholders from global countries to understand their e-commerce needs & translate that into scalable solution architecture on the SFDC platform using B2B Commerce Cloud. Define the e-commerce architecture blueprint & establish road maps to provide solutions that is scalable for global countries. Have overall experience of 10+ years as solution architect in order management / e-commerce / Storefront / Marketplace and at least 2+ years as solution / technical architect in Cloud Craze/Salesforce Commerce Cloud Expert level experience in defining B2B, B2C, B2B2C and related flavors of e-commerce models Must have worked with multi org environments for at least 2+ years Must have provided architecture guidance at global scale (10+ countries) for at least 2+ years Have thorough understanding on the Saleforce.com security model and have experience in at least one large scale implementation of communities Solid experience and knowledge on SSO security including oAuth, Open ID and SAML 2.0. Strong experience in designing the data models for products, pricing, invoices and orders Experience in major Salesforce.com technologies including Lightning, Canvas, Apex REST Services, Salesforce Connect, etc. Excellent skills in communicating with business stakeholders and technology teams At least one consultant / architect certification in Salesforce (e.g. CAA, CSA, Sales Cloud/Service Cloud) or from any other platforms

Evaluation and technical assessment of 3rd party Chemistry software solutions based on given requirements. Integration of 3rd party software solutions (cloud based and on-premise) into our existing application landscape. Definition, design and implementation of integration components and scientific software solutions. 8+ years of experience as Senior Software Engineer (with experience in Life Sciences) Strong expertise in the design of flexible, scalable and robust software solutions based on modern web technologies In-depth knowledge of Java/JEE technology stack​Experienced in the design and implementation of REST API's Good experience with the integration of Cloud-based and internal solutions into an existing application landscape (on-premise) Knowledge and hands-on experience with Big Data (e.g. Apache Spark, Hadoop) and No-SQL (e.g. MongoDB) database concepts Hands-on experience with Chemistry platforms and tools from at least one of the following vendors: Biovia, Chemaxon, Dotmatics and/or Perkin Elmer. Strong analytical skills combined with conceptual thinking and structured working style Excellent communication skills verbal and written in English Work experience in cross functional and multi-site teams

The company is a pharmaceutical/biotechnology industry. Drive the publication activities, e.g. submissions to peer reviewed journals, scientific and medical education activities at congresses Responsible for the development of patient focused educational materials Responsible for organizing and driving the medical education and internal communication activities at congresses Drive, coordinate and communicate activities related to pre-congress medical education materials, including e-learnings and others Responsible for the review and the approval process for grants, sponsorships and donations with educational intent Provide input and/or leads advisory board plans for assigned molecules/franchise Lead and deliver presentations during advisory boards and/or dedicated sections related to the relevant areas, e.g. publication and medical education Responsible for budget planning and tracking of the respective areas/activities in close collaboration with relevant colleagues Engage in regular prioritization, delegation and alignment discussions with vendors and monitor vendor performance based on cross-functional team assessments, aligned with procurement Professional experience in the pharmaceutical/biotechnology industry or related experience Medical affairs, clinical development or medical communications experience is preferred Experience in preclinical/clinical research, pharmaceutical project management and/or product marketing experience is a plus Experience in leading peer-reviewed publications or medical education/communications, in collaboration with scientific experts Experience in interpreting and presenting scientific data Experience in external agency management and in budget management is preferred Relevant therapeutic area experience preferred Understanding of drug development process and regulatory/legal environment for drug development and registration, clinical trials and medical communications is required Fluency in written and spoken English

You work very independently in projects, subprojects and take on support tasks within the SAP environment (module FI/CO); projects include the roll out of the group processes within SAP in international subsidiaries. Your main focus will be accounting. You are responsible for the definition and implementation of new business processes as well as optimisation of existing processes. As the contact person for the users, you provide exemplary support for complex tasks and be responsible from the analysis of the requirements to the creation of concepts until the go live of the tested solution. You have sound knowledge of business management and very good SAP knowledge, especially in modules FI and CO which you could deepen successfully over several years. Additional knowledge about the SD and MM interfaces is an advantage. Expect is a highly customer-orientated and resilient teamplayer with an independent working style and an analytical and connected mindset, who is ready to learn.

Die Firma agiert in der IT-Beratung. Aufbau und Leitung des Teams Platform Engineering Beratung von Kunden über den optimalen Einsatz neuer Plattformtechnologien Konzeption und Umsetzung im Bereich Platform Engineering auf Kundenprojekten im Umfeld von Private, Public und Hybrid Cloud Weiterentwicklung des Angebotes von adesso im Bereichen Platform Engineering (Cloud, Automatisierung, DevOps, Site Reliability Engineering) Weiterentwicklung des adesso-internen Technologiestacks Entwicklung von Prototypen und Showcases mit neuesten Plattformtechnologien Betreuung und Weiterentwicklung von Partnerschaften mit Technologieanbietern Erfolgreich abgeschlossenes Studium der Informatik oder vergleichbare Qualifikation Mindestens zehn Jahre Berufserfahrung im Bereich Softwareentwicklung oder Platform Engineering, davon mindestens fünf Jahre im Bereich Platform Engineering Mindestens dreijährige Erfahrung in der Führung eines kleines Team von Entwicklern oder Engineers Erfahrung in Entwurf, Entwicklung und/oder Administration von verteilten Systemen Erfahrung mit mindestens einer Public-Cloud-Plattform (AWS, Azure oder GCP), optimalerweise untermauert mit entsprechenden Zertifizierungen Erfahrung mit Container-Technologien (insbesondere Docker und Kubernetes, optimalerweise OpenShift) Erfahrung mit CI/CD-Tools (z.B. Jenkins, Spinnaker, TeamCity, Travis CI, Octopus, AWS Developer Tools, Azure DevOps) Erfahrung mit Umgang mit Infrastructure-as-Code (z.B. Vagrant, Terraform, AWS CloudFormation) Erfahrung mit IT-Automatisierungs- und Konfigurationsmanagement-Technologien (z.B. Ansible, Chef, Puppet) Erfahrung mit Tools für Performance und/oder Security-Monitoring (z.B. Graphite, Prometheus, Dynatrace, ELK-Stack, Splunk) Optimalerweise Erfahrung mit Integrationstechnologien und API-Management (z.B. Fuse, WSO2, Mulesoft, Kafka, Kinesis) Bereitschaft zur stetigen Weiterbildung Intrinsische Motivation zum selbständigen Experimentieren mit neuen Technologien Gute Beherrschung der deutschen Sprache mündliche und schriftlich, sehr gute Englischkenntnisse, optimalerweise gute Französischkenntnisse Reisebereitschaft innerhalb der Schweiz

Die Firma agiert in der IT-Beratung. Vertrieb von kundenspezifischen IT-Dienstleistungen und Softwarelösungen Eigenständige Projektakquise vom Erstkontakt bis zum Vertragsabschluss Akquise von Neukunden sowie Betreuung und Ausbau von Bestandskunden Laufende Kundenkommunikation und Projektbegleitung bis zur Implementierung inkl. Nachbetreuung Aufbereitung von ansprechenden Präsentationen und Reportings Kontinuierliche Analyse und Beobachtung des Marktes sowie Identifizierung von Marktpotenzialen Marketingaktionen initialisieren (Kunden- und Partnerevents, Workshops etc.) Erfolgreich absolviertes Studium, abgeschlossene Ausbildung oder vergleichbare Qualifikation Mehrjährige erfolgreiche Erfahrung im Vertrieb von Softwarelösungen und IT-Dienstleistungen Ausgezeichneter technischer Background sowie Verständnis für IT-Lösungen und komplexe Prozesse Ausgeprägte Markt- und Wettbewerbskenntnisse sowie Kontakte zu Entscheidungsträgern nationaler Unternehmen Souveränes Auftreten und überzeugungsstarke Kommunikations- und Verhandlungskompetenz in deutscher und englischer Sprache

Die Firma agiert in der IT-Beratung. Mitarbeit bei der Implementierung und Wartung von Mobile-Apps (Android/iOS) und Softwarekomponenten Teilnahme am gesamten Lebenszyklus eines Produkts, von frühen Konzepten und Prototypen bis hin zur vollständigen Implementierung Definieren von sauberem, sicherem und wiederverwendbarem Code Förderung guter Software-Engineering-Praktiken Aktive Teilnahme an den agilen Prozessen des Teams und des Unternehmens Teilnahme an der kombinierten Entwicklung mit iOS- und Android-Teams an verschiedenen Standorten Erfolgreich abgeschlossenes Studium der Informatik oder vergleichbare Qualifikation Erfahrung mit Mobiltechnologien (Android/iOS) Mindestens zwei Jahre Berufserfahrung in der Softwareentwicklung mit Java, Swift oder vergleichbaren Sprachen und im Entwurf von Mobilapplikationen Kenntnisse über Schnittstellen (REST und Web Services), iOS/Android-Frameworks und APIs Hervorragende Kenntnisse der modernen Software-Engineering-Grundsätze wie continuous integration, code reviews, test-driven development, refactoring and incremental delivery Hohe Kommunikationsfähigkeit und Gestaltungsvermögen, sowie sicheres und kundenorientiertes Auftreten Gute Beherrschung der deutschen Sprache in Wort und Schrift Reisebereitschaft

Die Firma agiert als das Finanzdepartement einer Schweizer Stadt. In dieser Funktion sind Sie tätig als Software Engineer im Bereich Web Frontend in einem agilen Produkt-Team. Sie arbeiten integriert in einem internen Softwareentwicklungsteam und wirken in diesem Team bei Aufbau und Weiterentwicklung von modernen E-Government Web-Lösungen mit. Realisieren von modernen mobilfähigen Web-Anwendungen und Web-Services Konzeptionelle und technische Ausarbeitung von innovativen Web-Lösungen Untersuchen von Anforderungen auf ihre Realisierbarkeit und Komplexität sowie auf deren Auswirkungen Ausbildung als (Wirtschafts-) Informatiker/in FH / Bachelor of Science (FH) oder höhere Fachausbildung mit mehrjähriger Erfahrung Offene und kommunikative Persönlichkeit Selbstständige, lösungsorientierte Arbeitsweise in einem agilen crossfunktionalen Team Freude an Projekt- und Teamarbeit sowie ausgeprägte Kundenorientierung Mehrjährige Erfahrung in Entwicklung von Responsive Desgin Web Anwendungen mit Angular Sehr gute analytische-konzeptionelle Fähigkeiten und eine hohe Lernbereitschaft Sehr gute Kenntnisse in Web-Frontend Technologien (Angular 5, Angular-Material, html5, CSS 3.0, JavaScript/TypeScript, JSON) Sehr gute Java Kenntnisse (mind. Java 7) Sehr gute API Kenntnisse (REST mit Java EE) Gute Kenntnisse in Test Automatisierung (z.B. Selenide, Protractor, JUnit) Gute Kenntnisse von Web-Technologien wie http(s) oder OAuth2/OpenID Connect Kenntnisse von (Applikation-) Servern (z.B. Wildfly, Apache, Tomcat) Erfahrung in Continous Integration (Jenkins) Erfahrung in SCRUM Von Vorteil: Kenntnisse in JIRA und Confluence Sie verfügen über sehr gute Deutschkenntnisse in Wort und Schrift

The company is a pharmaceutical company. Start date: asap Location: Basel Workload: 100% Duration: > 3 months Language: German  Active Directory (Troubleshooting experience) Microsoft KMS (License activation server) Terminal server (customer has several applications published) Active Directory Backup / Forest Recovery ADFS Azure AD Connect​ Automation Queries WSUS Windows patchingPowershell scripting Hyper-V environment SCCM troubleshooting deployment Operations Basics im Team Troubleshooting Quest Change Auditor (nice to have

Unterstützung unserer Kunden bei der Planung, Realisierung und Integration anspruchsvoller Anwendungen auf der Basis von Microsoft Technologien Konzeption, Design und Entwicklung in Softwareprojekten mit Webkontext Technische und konzeptionelle Beratung im Umfeld der .NET-, MVC- und vielleicht schon Angular-Technologieplattform Definition und Realisierung von komponentenbasierten Anwendungsarchitekturen Führen eines Scrum-Teams Abgeschlossenes Studium der Informatik oder vergleichbare Qualifikation Mehrjährige Berufserfahrung in der objektorientierten Softwareentwicklung Test Driven Development und Behaviour Driven Development sind Ihnen bekannt Praktische Erfahrung als Scrum Master Sehr gute Kenntnisse in den Microsoft Webtechnologien (.NET, MVC, WebAPI, Angular, Javascript, Typescript) Sicherer Umgang mit Microsoft Visual Studio und Team Foundation Server Gute Kenntnisse im Umgang mit dem Microsoft SQL Server Sicheres und kundenorientiertes Auftreten Gute Beherrschung der deutschen Sprache in Wort und Schrift Reisebereitschaft

Plan and carry-out analytical tests according to current good manufacturing practices (cGMP) standards on drug products in clinical development or commercial phase (specifically focused on HPLC and CE purity methods, content by UV, identity, color, clarity and opalescence, pH, osmolality, extractable volume, CCI, visible particles, subvisible particles and related DP analytics) Contribute to planning of analytical method validation as well as execute and evaluate validation experiments Support cGMP regulated analytical method transfer Ensure proper maintenance of equipment, safety and health protection following lab and safety instructions and all cGMP regulations Install, qualify and maintain instruments according to best practices and regulations Support establishment of DP analytical infrastructure and services for biologics, small molecule and peptide parenteral products for clinical and commercial products Completed vocational training as BTA, PTA, CTA or equivalent or a degree as B.Sc. in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related subject Extensive working experience as a technical assistant in the pharmaceutical or chemical industry, preferably in analytics Strong working knowledge in majority of relevant analytical techniques Very good reporting, interpretation and documentation skills of scientific results Good knowledge of written and spoken English Experience working in a cGMP-regulated environment is advantageous Proficiency in development of parenteral dosage forms and protein analytics is beneficial

Planung und Durchführung von Entwicklungstasks inklusive Unit Tests Priorisierung des Backlogs in Zusammenarbeit mit eManor und dem Delivery Team Aufwandsschätzungen für einzelne Entwicklungstasks Definition der Software Architektur Schulung interner Mitarbeiter in Bezug auf Backoffice Funktionalitäten Führung und Koordination von externen Dienstleistern Sie verfügen über einen Hochschulabschluss in Informatik (Bachelor/Master) Mehrjährige Erfahrung in der Rolle als Senior Entwickler und Software Architect, vorzugsweise im Bereich eCommerce Sie bringen über fundierte Programmier- und Systemkenntnisse (Spring, Java/J2EE, HTML, CSS, moderne Javascript Librariers, Linux) mit Sie sind vertraut mit der Architektur von Multi-Tier Webapplikationen sowie den gängigen Entwicklungsmethoden (wie zum Beispiel Continuous Integration, automatisiertes Testing, Code Metrics) Sie besitzen grosses Interesse an technischen Neuerungen und sind eine konzeptionell versierte sowie detailorientierte Persönlichkeit mit einem hohen Qualitätsbewusstsein Sie zeichnen sich durch einen ausgeprägten Teamgeist, kommunikative Fähigkeiten, Belastbarkeit und ein vernetztes Denkvermögen aus Eine problemlose Verständigung in Deutsch und Englisch ist Voraussetzung für diese Position

Die Firma agiert in der IT. Analyse, Spezifikation, Design und Entwicklung des Warehouse Management Systems Weiterentwicklung des bestehenden Frameworks in JAVA Selbstständige Erarbeitung von Lösungsvorschlägen Dokumentation der Softwarelösung Coaching der Entwickler und permanente Qualitätssicherung des Produktes Erarbeitung und Durchsetzung von Architektur- und Projektabwicklungsrichtlinien Implementation von Kundenanforderungen in komplexen Logistikprojekten Abgeschlossenes Hochschulstudium (FH/ETH) in Informatik/Elektrotechnik Mehrjährige Erfahrung als Senior Software Engineer und Architekt Ausgezeichnete Kenntnisse der objektorientierten Softwareentwicklung in JAVA Erfahrungen mit Eclipse, Spring, Hibernate, QueryDSL, XML, Maven, Oracle SQL, . . Gute Datenbankkenntnisse, vorzugsweise Oracle, MSSQL oder PL/SQL wünschenswert Initiative, lösungsorientierte und teamfähige Persönlichkeit Konzeptionelles Denkvermögen und schnelle Auffassungsgabe Methodische und strukturierte Arbeitsweise Ausgezeichnete Deutsch- und gute Englischkenntnisse Erfahrungen in der Logistikbranche

The company is a Scientific firm. Applies Good Manufacturing Principles in all areas of responsibility. Demonstrates and promotes company vision. Performs all activities in a safe and efficient manner. Oversees and manages the teams responsible for Quality Control and Quality Assurance Batch Record Review Ensures the pharma unit maintains the highest quality standards and are compliant with all regulations/procedures by driving continuous improvement activities. Provides leadership in promoting and enforcing GMP and company quality Resolves issues potentially affecting product quality/compliance. Evaluates and develops techniques designed to maintain awareness of SOP's and cGMP requirements. Maintains excellent client relationships by providing a technically competent QC and QA department Perform job performance reviews and own full performance management cycle of direct reports Identifies risks and performs trending of complaints, deviations, and audit findings, and identifies appropriate corrective and preventative measures for the Pharma Unit Escalates quality events (as necessary) to QA Director and works with QA Director to periodically review significant aspects of site quality performance Interacts with clients on quality issues and is an advocate of the company's quality concept. Implements and monitors key performance indicators (KPI's) within area of responsibility. Develops process improvement ideas for the Pharma Unit Provides or assists on employee training to ensure compliance with procedures and regulations. Supports and assists on regulatory and client audits. Participates in self-inspection activities Assist in conducting investigations, when needed. Supports Quality Council and Global Quality Leadership Team initiatives. Other duties may be assigned to meet business needs. Responsible for supervising, training, and motivating direct reports. Conducts all activities in a safe and efficient manner. A minimum of 5-8 years of experience in the Pharmaceutical or related regulated industry and at least 5 years of direct managerial experience required. Experience with Quality Systems (Change Control, deviations, complaint management, documentation management, audits, self-inspections, etc.) Must have a sound understanding of cGMPs. Capable of effectively managing 3-10 direct reports in a dynamic environment. Effective communication skills to interact with employees in all departments of the organization including, but not limited to, managers, senior management, customers, vendors, and regulatory agencies. High ethical standards required to uphold compliance. Sound knowledge of pharmaceutical operations Strong leadership ability. Comfortable with decision-making on diversified issues and communicating directly with customers on a routine basis. Good organizational skills Mastery of skills required to read, understand, and adhere to the SOPs and policies of a GMP environment. Can manage personnel in a cGMP environment May be required to travel domestically and internationally. Ability to manage multiple tasks and meet deadlines, work under pressure in a fast-paced environment. Applies Good Manufacturing Principles in all areas of responsibility. Demonstrates and promotes the company vision. Support other related tasks as required. Familiarity with Six Sigma, Lean, Practical Process Improvement, etc is a plus.

The firm is a Pharma company. ● Provide Subject Matter Expertise for Quality Computer Systems (e.g., QMS, EDMS, ECM) ● Ensure GMP Computer Systems and their operation are in compliance and fit for intended use according to applicable procedures ● Approve major upgrades and the replacement and/or retirement of computerized systems through change management processes ● Oversee system access process / procedures including periodic review of user access lists ● Determine how to verify data integrity and propose strategies to achieve better data accuracy ● Manage the escalation of issues to Business or IT and communicate/document status of issues where appropriate ● Give input into and help define validation test strategy ● Works with management to align projects to strategy and business objectives ● Serves as ambassador for measurement, accountability and a disciplined approach to process improvement within the departmentand across functional area ● Lead or participate in interdepartmentalteams, process improvements, or new system design ● Leads meetings and or represents organization on projects, support and/or significant issues ● Make informed decisions on software issues in collaboration with key stakeholders and abiding by system requirements ● Ensure the smooth introduction of new functionality of the software as they are added ● Regularly evaluate business use of the software and training materials to ensure alignment according to intended use ● Initiate, investigate and close complex investigations and discrepancies ● Lead or participate User Group Forums both locally and across sites ● Attend or present at Vendor User Group Conferences ● Possess analytical and/or computer skills sufficient to: ● Understand data requirements and interdependencies ● Solve problems through effective troubleshooting and suggest viable solutions ● Continuously improve systems achieving increased compliance and efficiency ● Use influence rather than authority when necessary to achieve results ● Bachelor's Degree in an applicable field or equivalent, MBA a plus ● Minimum 7-10 years of work experience in biopharmaceutical production and an understanding of quality processes and procedures ● Experience with validated or controlled environments preferred ● Demonstrated proficiency in Software Development Lifecycle (SDLC) ● Working knowledge of one or more information packages (e.g., QMS, EDMS, ECM) ● Experience using Lean Production System (LPS) for continuous improvement opportunity evaluation ● Leadership and project management, including understanding of life cycle planning ● Demonstrated ability to influence and lead both with and without authority ● Strong interpersonal skills and the ability to work well with others in a proactive, positive and constructive manner ● Flexibility in problem solving, providing direction and work hours to meet business objectives

The firm is a molecular entities in our global clinical pipeline. Ensure DGM function collaborates with various internal partners Build and maintain paper and electronic clinical document technical standards meeting internal and external requirements. Define and lead development of clinical document management processes, archiving solutions and related processes and strategies to follow HA guidelines, Good Clinical Practices and Novartis SOPs. Own related SOPs or delegate ownership Set priorities, decide work load distribution, forecast demand and drive resource / budget planning to ensure adequate delivery of document management services. At least Bachelors degree in related scientific discipline (natural, pharmaceutical, medical, archival or information technology). At least 14 years of significant experience in clinical research / pharmaceutical industry and in leading people, teams and projects Demonstrated experience handling delivery from vendors, audit program, governance. Strong experience of the clinical drug development and international drug approval processes and related document requirements. Good Project Management skills and interpersonal skills

Die Firma agiert in der IT. Ein tolles Team und eine angenehme, lockere Arbeitsatmosphäre Viel Erfahrung, Qualifikation und Knowhow Professionelle Projektdurchführung und strukturierte Arbeitsabläufe Interessante und abwechslungsreiche Projekte Offene Unternehmenskultur, kurze Entscheidungswege und flache Hierarchien Die Chance, den Ausbau und die Ausrichtung unserer Firma mit deinen Ideen aktiv mitzugestalten. Individuelle Weiterbildungsmöglichkeiten und entsprechende Unterstützung Microsoft-Zertifizierungen Flexible Arbeitszeiten Abgeschlossenes Studium im Bereich Informatik Sehr gute Kenntnisse im .NET Framework (3.5 - 4.7) Sehr gute Kenntnisse in Visual Studio, TFS Idealerweise (erste) Erfahrungen mit folgenden Technologien und Themen: WPF, WCF, ASP.NET, Azure, Windows Phone SDK, Xamarin Leidenschaft für Softwareentwicklung Eigenständigkeit, Engagement, Lernbereitschaft, Kommunikationsfähigkeit und Teamgeist Grundsätzliche Reisebereitschaft Sehr gute Deutschkenntnisse Gute Englischkenntnisse

Vielfältige Aufgaben im gesamten Softwareentwicklungsprozess (Architektur, Analyse,​Design, Programmierung, Tests, Schulung, Einführung) Software-Architektur und Solution Design bei Neu- und Weiterentwicklung von SoftwareLösungen Unterstützungsaufgaben im Entwicklungsteam Bei Eignung sind auch Teilprojekt- oder Projektleitungen möglich Abgeschlossenes Studium an einer Universität / Hochschule und/oder entsprechende langjährige Erfahrung in der Informatik Sehr gute Kenntnisse und Praxiserfahrung in der Entwicklung von Java Enterprise Applikationen mit Java EE (JPA, CDI, SOAP und REST Services) oder Spring. Kenntnisse von modernem Web-Applikationen mit gängigen App Frameworks (Angular von Vorteil) Fundierte Kenntnisse in der Software-Architektur inkl. Analyse, Design, Implementierung und Deployment Gute Kenntnisse von relationalen Datenbanksystemen (SqlServer, DB2, Oracle) Gutes Wissen und Praxiserfahrung in agilen Software-Entwicklungsmethoden (SCRUM). Selbständige Arbeitsweise, Kundenorientierung, Flexibilität und gute Kommunikationsfähigkeiten sind uns sehr wichtig Sehr gute Kenntnisse in Deutsch, gute Kenntnisse in Englisch und Französisch (jeweils in Wort und Schrift) von Vorteil

The company is a global leader in the healthcare. Conducting risk-based audits of R&D, Supply Chain and Business Development units and their processes in Pharma and Diagnostics Perform risk assessments, develop and adapt work programs Evaluate governance, risks and controls in the processes reviewed and agree on appropriate action plans with management in order to improve effectiveness and efficiency as well as to mitigate risk exposure Support more junior auditors during audit engagements The position involves a fair amount of travel world-wide (up to 50%) Solid academic credentials in natural sciences or a medical degree. Approximately 5 years of practical business experience in R&D in pharmaceutical or diagnostics industry outside of Quality and Compliance functions. Alternatively, you have a strong background and experience as data scientist in biostatistics Demonstrated negotiation and influencing skills as well as ability to convey difficult messages clear and constructively Your English allows you to converse fluently and concisely, which leads to efficient interviews. Your written reports are clear, concise and easy to read Strong team skills and you enjoy working in an international environment and different cultures

The company is a Pharma firm. •Provide clinical leadership and medical strategic input for all clinical deliverables in the assigned project or section of a clinical program if applicable. Clinical deliverables may include clinical sections of individual protocols consistent with the Integrated Development Plans (IDP), clinical data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications •Lead development of clinical sections of trial and program level regulatory documents (e.g., Investigator's Brochures, briefing books, safety updates, submission dossiers, and responses to Health Authorities) •Drive execution of the section of the clinical program in partnership with global line functions, assigned Global Trial Directors, and regional/country medical associates if applicable •Oversee/conduct ongoing medical and scientific review of clinical trial data with Clinical Scientific Expert(s) •Support (Sr.) Global Program Clinical Head in ensuring overall safety of the molecule, may be a core member of the Safety Management Team (SMT), and support overall program safety reporting (e.g., Periodic Safety Update Reports (PSURs), Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with Patient Safety •Support the Therapeutic Area Head (TAH) by providing medical input into IDP and CTP reviews and giving/driving development of disease clinical standards for new disease areas. •As a medical expert, supports the (Sr.) Global Program Clinical Head or TAH in interactions with external partners (e.g., regulatory authorities, key opinion leaders, data monitoring boards, advisory boards, patient advocacy groups), internal stakeholders (e.g., CTT, Research, Translational Medicine, Global Medical Affairs, Marketing, HE&OR), and internal decision boards •Medical Degree required, ophthalmologist preferred. Advanced knowledge and clinical training required with Medical Board Certification •≥ 5 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV. ≥ 3 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry •Demonstrated ability to establish strong scientific partnership with key stakeholders •Detailed knowledge of GCP, clinical trial design, statistical analysis methodology, and regulatory/ development process •People management experience preferred, this may include management in a matrix environment. Global people management experience desirable •Strong interpersonal skills and excellent negotiation and conflict resolution skills

Die Firma agiert in der IT. Entwicklung integrierter kundenspezifischer Lösungen auf Basis von Java EE und Open Source Technologien mit Verwendung eines abwechslungsreichen Technologie Stacks (z.B. Neo4j, Spring Cloud, React und AngularJS) Analyse und Bewertung fachlicher Anforderungen, Erstellung von Lösungskonzepten sowie Customizing und Go-Live Betreuung Eigenständige Beratung und Schulung der Kunden in Technologien, Methoden und prozessorientierten Anwendungen Design von CI-/CD-Prozessen zur automatisierten Softwareentwicklung Flexibler Einstieg an einem der Standorte ganz nach dem Motto „Home is where your heart is" Onboarding an unserem Hauptsitz mit Trainings, Tech Talks und Networking Events Individuelles Weiterbildungskonzept inklusive Mentoring, dem Besuch von Konferenzen sowie Ablegen von Zertifizierungen​(z.B. Weiterbildung zum zertifizierten Softwarearchitekten) Teamgeist und Spass an der Arbeit gestärkt durch zahlreiche Events wie Grill'n'Chill, Marathon, Kartmeisterschaft und Hackathon

Lead all techno-functional aspects of the SAP S/4 HANA Central Finance implementation, in close collaboration with Finance leadership and internal and external suppliers Ensure design decisions meet immediate requirements and are aligned with long-term strategic needs Apply agile methodology and maximize speed-to-value Closely partner with Finance leaders to drive technology innovation Monitor the technology landscape and propose solutions that advance how Syngenta operates Evaluate technologies, align stakeholders on solutions and contribute to the overall technology roadmap Develop business cases for new projects or enhancements, and ensure successful project initiation and executio Expert SAP ERP functional / configuration knowledge in at least 2 Finance process areas Min. 5 years' experience successfully executing complex ERP implementation projects Broad expertise and good overview of Finance related process areas (A2R, P2P, O2C, Tax, Treasury, Product Costing, and Financial reporting, etc.) including supporting SAP and non-SAP technologies Solid understanding of ERP architecture and basis technologies SAP S/4 HANA experience is not required but preferred Experience applying novel technologies in Finance (artificial intelligence, cognitive technologies, and robotic process automation) Strong business analysis and project management skills; experience applying agile methodology is a plus Ability to drive outcomes and operate hands-on when needed Strong written and verbal communication skills in English

Die Firma agiert in der IT. Sie konzipieren, erstellen und designen Datenmodelle Sie implementieren unternehmensweite Reportinglösungen Sie optimieren Berichte und Applikationen Sie arbeiten am internen Know-How Aufbau mit (Fachthemen und Technologien) Sie haben ein abgeschlossenes Studium der (Wirtschafts-) Informatik, Mathematik, Betriebswirtschaft oder eine vergleichbare Qualifikation/ Ausbildung. Kenntnisse im Umfeld SAP HANA sind wünschenswert aber nicht zwingen. Sie verfügen über analytisches Denkvermögen, arbeiten lösungsorientiert und schreiben kundenorientierten Service groß.

The company is a pharma firm. Establish Drug Product analytical infrastructure and services for biologics, small molecule and peptide parenteral products for clinical as well as commercial products Install, qualify and maintain instruments for Drug Product Phys-Chem Analytics and QC in close alignment with current best practices and regulations Develop and establish analytical methods and technologies to support formulation development and Drug Product Quality Control (including HPLC and CE purity methods, content by UV, identity, color, clarity and opalescence, pH, osmolality, extractable volume, CCI, visual inspection, subvisible particles) Carry out Phys-Chem analytical tests to support formulation development and Drug Product Quality Control as required, possibly under GMP, following applicable SOP's and all current documentation practices Ensure proper maintenance of equipment, safety and health protection following lab and safety instructions and all cGMP regulations Training on the job as analytical lab technician or a degree (BSc, MSc) in e.g. Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related discipline Working experience as a research/ technical assistant in the pharmaceutical or chemical industry, preferably in analytics Good working knowledge in relevant analytical techniques as well as with parenteral dosage forms and protein analytics Experience in reporting, interpretation and documentation of scientific results Good communication and inter-personal skills; Ability to work independently in a team Good knowledge of written and spoken English

As one of the leading suppliers at our banking client, Swisslinx are looking for a highly motivated and outgoing SAILPOINT Administrator with SAILPOINT IdentityIQ or IdentityNow experience for a challenging 12 month contract role in Basel, Switzerland (with possibility to extend up to five years). Our client is increasing the size of their small and experienced Cyber Security team. In this role you would be responsible for supporting the bank's identity governance platform based on SAILPOINT IdentityIQ, including basic maintenance of the application, such as the customized logic and rules deployed in the system. Reporting to the Head of Security Engineering and Architecture, you will also work closely with the bank's Access Management team in order to define process and procedures for identity governance. As a passionate IT security specialist you, you will possess the following skills and experience: •¢ Experience in a role within Identity Management (IDM) or Identity Access Management (IAM) domain as a consultant or analyst •¢ Proven experience working with SAILPOINT IdentityIQ or SAILPOINT IdentityNow •¢ Programming knowledge, ideally with Java or other OO languages •¢ Understanding of Role Based Access Management concepts •¢ Knowledge of Identity Governance activities •¢ Scripting in PowerShell •¢ Experience with some of the following technologies strongly advantageous: Microsoft SQL Server, Windows Server 2016, Apache Tomcat •¢ You are a self-starter and have the ability to pick new concepts up quickly •¢ Very good communication and presentation skills and ability to deal with stakeholders and vendors •¢ Outstanding problem solving skills and analytical approach •¢ Fluency in English (additional languages a plus) Are you interested to work in an international environment in one of the leading financial companies worldwide? Then apply now! We look forward to receiving your full application. By applying for this position, I consent to the Swisslinx Group of companies: - storing my personal information (including name, contact details, Identification and CV information etc.) on their internal or external servers for the purpose of informing me of potential employment opportunities - using my personal information or - supplying it to third parties upon express consent for the purpose of informing me of potential job opportunities - transferring where applicable my personal information to a country outside the EEA/EFTA I also hereby agree to the Swisslinx privacy policy () and Terms of Use ()

Listing only available in German. Zur Verstärkung unseres Teams suchen wir eine/n Schiffsführer/-in ms rhystärn (Arbeitspensum 60 - 100%) Gesamtverantwortung für die Sicherheit an Bord des Schiffes Führung der Schiffe ganztags, am Abend und an den Wochenenden Schiffseinsätze gemäss Einsatzplanung Übermitteln aller Fahr-..... klicken sie bewerben, für die volle Stellenbeschreibung

Die Firma agiert in der Beratung. Bereitstellung technischer Lösungen zur Erfüllung von Geschäftsanforderungen in der BW-Entwicklungssprache von SAP Entwerfen, entwickeln, konfigurieren, migrieren, testen und implementieren Sie Data Warehousing-Lösungen für SAP BW 7.x. Entwerfen und Erstellen von Datenflüssen, einschließlich InfoObjects, InfoCubes, Aggregaten, Datenspeicherobjekten (DSO), MultiProvidern, InfoSets, Transformationen, DTPs und DataSources Erstellen, testen und veröffentlichen Sie BEx Reports, BEx Workbooks und BEx Web Applications mit der SAP BEx 7.x Suite Variablen entwickeln, Kennzahlen einschränken, Kennzahlen, Strukturen und Selektionen im SAP BEx Query Designer berechnen Entwicklung, Erweiterung, Test und Implementierung von SAP-ABAP-Anwendungen Funktionsbausteinextraktoren in ABAP entwickeln Verschieben Sie vorhandene Abfragen in HANA Views Über 7 Jahre Erfahrung in Design, Modellierung und Entwicklung in SAP BW 7.0 oder höher SAP ABAP Programmierkenntnisse Ausgezeichnete schriftliche und mündliche Fähigkeiten Ausgeprägte Kenntnisse und Erfahrungen in den Bereichen Analyse, Fehlerbehebung und Problemlösung beim Analysieren und Verstehen von Geschäfts- / Technologiesystemarchitekturen, Datenbanken und Clientanwendungen Erfahrung mit der Finanzberichterstattung im BW Möglichkeit, mit Anwendern aus Wirtschaft und Technologie zusammenzuarbeiten, um Berichts- und Analyseanforderungen zu definieren und zu erfassen Erfahrung im internationalen Unternehmensumfeld Teamspieler an eine agile Umgebung gewöhnt Sehr flexibel, keine Schwierigkeiten, sich an neue Situationen / Herausforderungen anzupassen

The company is a pharma firm.  Provides direction and leadership to one or more clinical operations teams (depending on competency level, the International Clinical Trial Manager may not have leadership responsibilities): Develops operational plans including site monitoring strategies, risk mitigation strategies, trial budgets, site selection, and clinical supplies management; Builds effective and efficient high performing operations teams and ensures team members are aware of their accountabilities, responsibilities and deliverables; Creates team culture and promotes team spirit; Leads, develops and maintains effective working relationships with the Study Management Team members, with particular focus on affiliate teams, external providers and collaborative partners; In collaboration with functional management, coaches, supports, and provides study specific direction to Study Management Team members; Oversees the development and maintenance of study specific manuals created by the International Clinical Trial Associate. Responsible and/or Contributes to the development and management of the study timelines, resources, budget, risk and quality plans: Responsible to identify and update operational tracking tools, including systems to meet the needs of the operations team and ensures reporting to the International Clinical Program Leader; Develops and manages clinical study budgets. Communicates variances in the budget and action plan for resolution to the International Clinical Program Leader (ICPL); Establishes study milestones and ensures accurate tracking and reporting of study metrics. Provides clinical operations expertise to ensure operational feasibility and delivery: Develops the site feasibility questionnaires and creates the study level patient recruitment plan and retention strategies based on feasibility data and input from the CRO and affiliates and in consultation with the ICPL; Analyses the feasibility data across countries with input from the affiliates and provides the strategic country and site distribution and patient numbers to the ICPL; Provides operational input and insight into all study related documentation (including protocol and informed consent form) and processes. Oversees forecasting of clinical/non-clinical supplies: Designs drug assumption and supply chain process in partnership with Drug Supply Coordinator, affiliates and International Clinical Program Leader; Oversees the forecasting and management of non-clinical supplies to ensure sites have supplies to run clinical study. Delivers the operational elements of the study plan: Leads and chairs operations team meeting and organizes the investigator meetings, monitor training, CRO kick-off meetings (depending on competency level); Ensures that safety reporting is established and maintained for the duration of the study and that reporting timelines are met; Proactively manages actual study level recruitment versus planned patient recruitment status and communicates variance to the International Clinical Program Leader and implements contingencies in consultation with the International Clinical Program Leader; Primary contact with CRO and affiliates to maintain oversight of performance, issues, and their resolution and identify systematic issues and coordinates any corrective action; Ensures the completion and finalization of any corrective and preventative action plans resulting from internal site audits; ensures inspection readiness of the study at all times; Oversees the maintenance of drug supplies and resolution of issues with input from Clinical Drug Supply coordinator; Coordinates responses to study questions or issues from Health Authorities or IRBs/IECs; Develops, obtains endorsement and oversees the SMT goals, and makes sure that all efforts are made by the extended SMT to achieve them on time. Provides the day-to-day operational management of CROs and vendors to ensure delivery against contracted scope of work: Performs ongoing vendor management (e.g., CROs, Central Labs, IVRS, Reading Centers), including independent negotiation of scope of work, budgets, performance management, and issue resolution; Develops and executes appropriate site and CRO/vendor audit and quality plans in collaboration with Product Development Quality. Identifies areas of best practice and process improvements: Participates in initiatives and programs as assigned; Maintains oversight and ensures consistency of the operational aspects across studies within a project. Ensures study adherence to ICH/GCP and SOPs: Is responsible for acting in line with legal, regulatory and company standards and codes of practice; Completes all required training modules as a priority.          Life sciences degree and at least 8 years of experience in the pharmaceutical industry; Solid experience managing global clinical studies, ideally within Inflammation/Infectious/Ophthalmology therapeutic areas; Proven clinical development experience and managing operational aspects of all stages of clinical studies, preferably working in a Global environment; Experience in Non Interventional studies is a plus Previous experience working with vendors and CROs, drug supply management; Ability to work across organization at all levels; Proven ability to successfully achieve results within a multi-cultural and geographically diverse team; Well developed analytical and oral written communication skills demonstrated by an ability to present clear instruction/direction to teams at the same level in the organization and influence at higher levels in the organization; Experience of working as part of a large team and leading small study or functional teams, with a proven ability to be an active member of the team and motivate and lead a small team to deliver against commitments; Experience of project managing operational aspects of a clinical study including development of timelines, budgets and resource plans; Fluency in written and spoken English.

The company is a pharma firm. You lead a section of medicinal chemists supporting drug discovery projects in the areas of Inflammation and Immunology, Infectious Diseases, Neuroscience, Ophthalmology and Oncology You provide a holistic portfolio perspective and high level scientific leadership to teams with regards to prioritizing and executing on key deliverables, project needs and resourcing You build strong collaborative partnerships to align stakeholders on the capabilities and resources for the support of current SMR projects and future pRED portfolio You develop a long-range course of actions or set of goals to align with the medicinal chemistry's vision You keep abreast of disruptive and novel technologies, and lead emerging scientific initiatives related to drug discovery You develop, mentor and retain talents through constructive feedback and encouragement You build and support high impact working teams acting in a flexible and agile manner while encouraging a culture of inclusiveness, authenticity and smart risk taking. You foster a culture of mutual support, cross-training, continuous learning and self-organization while strengthening commitment to lab work. You may act as an SMR representative to the drug discovery teams within the Roche R&D governance to influence and build the research portfolio You may participate in assessment of business development opportunities Experience in leading project teams up to clinical candidate selection including experience in global research and development teams. You have been successful as a group, section head or director with emphasis on developing and coaching scientists to build a high performing team. You are an authentic inspirational leader, acting with a clear sense of purpose and able to effectively cope with change, handle risk and uncertainty Deep medicinal chemistry knowledge and expertise, coupled with a state of the art knowledge of med-chem informatics and computational tools with a bold vision of the future Strong track record, extensive medicinal chemistry experience and a detailed understanding of disease biology and target landscapes Willingness and ability to work in a dynamic, diverse, multicultural and multi-disciplinary environment Excellent communication and influencing skills: you are able to position your ideas and share knowledge in matrix environments and to influence others across interfaces Ability to anticipate the impact of change, guide others to see the opportunity in change and challenge the status quo Commitment to enable self-organized teams to draw on the full capabilities of the organisation to meet project and functional achievements

Azure DevOps Engineer vacancy for a globally operating Basel based company in the financial services sector. Your experience/skills: Strong Azure DevOps Server experience (TFS - Team Foundation Server) Proficiency in DevOps engineering with profound knowledge of the entire DevOps stack including CI and CD Familiarity with secure software development lifecycle and secure coding practices such as OWASP is advantageous Understanding of static analysis used for security testing is beneficial Bachelor degree in an IT related field is desirable Languages: English, fluent in written and spoken Your tasks: Monitoring and supporting the on premise installation of Azure DevOps Server 2019 Assisting the development teams with implementing CI/CD pipelines and agile project methodologies Designing a new DevOps offering according to established business requirements and IT vision Ensuring the successful delivery of the platform by collaborating closely with both IT and business teams as well as communicating and engaging with key stakeholders Documenting DevOps architecture, key decisions, processes and environments along with preparing and delivering presentations and demos Start: 10/2019 Duration: 06MM+ Location: Basel, Switzerland Ref.Nr.: BH14834 Does this spark your interest? Then take the next step by sending us your CV as a Word document and a contact telephone number on which you are reachable during working hours. Going the Extra Mile. As a preferred recruitment agency for Swiss banks, international insurances, finance service providers, software and pharma companies, we acquire exciting positions since 1998 in Zurich, Bern, Basel and other regions in Switzerland every day. Due to work permit restrictions we unfortunately can only consider applications from EU or Swiss citizens as well as current work-permit holders for Switzerland. New to Switzerland? In case of a successful placement, we support you with: All administrative questions Finding an apartment Health - and social insurance Work permit and much more Thank you for your interest. By applying, you give us the permission to internally store and process your data for the application process. We strictly comply with the applicable data protection laws.

The company is a pharma firm.  Contribute to the design, management and maintenance of biomedical (including clinical trial) data standards from protocol development to regulatory submission Help to identify the needs of key stakeholders and assist in the prioritization of new clinical data standards for inclusion in the Data Standards & Governance (DSG) Roadmap Lead the development of new biomedical data standards from protocol development to regulatory submission Support the technical implementation and adoption of biomedical data standards Active role in the governance of biomedical data standards Contribute to the curation and integration of data for the creation of data marts: Provide guidance to key stakeholders relating to transforming previously collected biomedical data to the appropriate data models Help to maintain content in the Global Data Standards Repository (GDSR) Develop and deploy metrics that assess the usage and value of the biomedical data standards Drive adoption of biomedical data standards from external standards development organizations (SDOs) such as CDISC, HL7, ISO: Actively monitor and assess standards being produced by SDOs Serve as a member of the SDOs Actively promote and leverage knowledge sharing with standards experts within Product Development, more broadly across the Roche group and the industry as a whole BS/BA or MS in computer science, mathematics, statistics, or related areas of Clinical Research Experience in pharmaceutical industry, including standards development or implementation within a Biometrics field Experience with CDISC ADaM and other industry standards, possibly including CDISC CDASH, SDTM and/or Controlled Terminology Previous experience as a Study Statistician or Statistical Programmer is a plus Knowledge of a specific therapeutic area or disease area is a plus

Die Firma bietet professionelle iT Dienstleistungen für den verantwortlichen Betrieb unternehmenskritischer Plattformen. Beratung und Anleitung des Projektteams in der Anwendung neuer Patterns (Event-Driven, Cloud-Native, Microservices, CI/CD, Domain Driven Design u.a.) Sicherstellung von Performance, Security, Wirtschaftlichkeit sowie Einbettung in die Anwendungslandschaft und Unternehmensarchitektur Aufnahme der fachlichen Anforderungen und Umsetzung in IT-Lösungen Analyse von Problemstellungen und Erstellung von technischen Spezifikationen Erfolgreich abgeschlossenes Studium der Informatik oder vergleichbare Qualifikation Mindestens drei Jahre Berufserfahrung in der Softwareentwicklung mit Java Erste Kenntnisse in der Entwicklung von Applikationen mit Microservices, Docker, Kubernetes, Vertx und Kafka, Openshift Fundierte Kenntnisse in der Anwendung von Methoden und Techniken des Softwareengineering wie Prozess- und Datenmodellierung (OOA/OOD und UML) Gute Kenntnisse gängiger moderner Komponentenmodelle (JEE) und Entwurfsprinzipien (Domain Driven Design) Gute Kenntnisse in der Anwendung von Vorgehensmodellen der Softwareentwicklung, bevorzugt in agiler Entwicklung (Scrum) Gute Kenntnisse aktueller Frameworks wie z.B. Hibernate, Spring, Angular oder/und React Umgang mit relationalen und nicht-relationalen Datenbank-Systemen Hohe Kommunikationsfähigkeit und Gestaltungsvermögen sowie sicheres und kundenorientiertes Auftreten Gute Beherrschung der deutschen Sprache in Wort und Schrift

We Offer A dynamic position as Client Service Advisor within our Ship Finance team where you contribute in an international working environment with experienced and highly motivated specialists The main focus of this role is the administrative management of a loan portfolio in the ship finance sector including its monitoring as well as risk-related and compliance issues but also collection of required documentation You perform Due Diligence in respect of credit, KYC, AML and reputational aspects as part of the onboarding process of new clients and periodic reviews of the existing ones You also have the possibility to collaborate with clients and lawyers when reviewing a variety of loan documents You take over the responsibility for credit operations and loan closings and ensure a compliant process of all relevant conditions You assist and support Key Account Managers in the preparation of credit applications for the attention of the credit decision authority and periodically evaluate existing loans You ensure at all times that all credit related data are updated and correct in the respective internal database systems. You join a highly motivated and forward-thinking team passionate about ship finance, whose team spirit and specific expertise guarantees an exciting working environment and growth opportunities Through close collaboration with internal partners and departments we offer you the chance to build up a strong and sustainable network within the bank You Offer Are you looking for a new challenge and describe yourself as a committed standout colleague with the dedication to deliver high quality work within short timeframe? Do you show initiative and a solution oriented thinking? Then we are sure that you would be an excellent fit for our team Banking apprenticeship with further education such as FH or equivalent education; business administration or law is a plus Prior experience in the international (asset) finance segment is an advantage As an astute problem solver, you possess strong analytical skills and are passionate about working with numbers enabling you to work multi-functionally in order to arrive at the best way forward for our team Excellent knowledge of Microsoft applications, proficiency in Excel You demonstrate high sense of responsibility, pro-activeness and ownership You show high perception and interpersonal skills as well as discretion and affinity to client contact You are able to build trusting and positive relationships with a wide range of colleagues and to create a network with senior business partners Fluency in English, with good German skills being an advantage *LI-CSJOB* Ms. V. Thoma would be delighted to receive your application. Please apply via our Career Portal.