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Amaris is an independent, international Technologies and Management Consulting Group. Created in 2007, Amaris is already established in over 50 countries and supports more than 850 clients worldwide throughout their project's lifecycle. Our expertise covers five areas of innovation: Business and Management, Information Technologies, Engineering and High Technologies, Telecommunications and Biotech and Pharma. With more than 65 offices across the world, the Group offers proximity support to its clients in all their locations and many opportunities of international careers for employees. In 2019, Amaris aims to reach a turnover of 350 million euros, 6500 employees and to develop its workforces with the anticipation of a further 2000 new job openings. We expect to triple our workforce within the next few years and reach a leading international position in independent consulting.  Your Role  For one of our most important clients operating in the pharma/chemical sector, we are looking for IT consultants/managers experts in process optimisation and digitalisation.  The selected people will join a dynamic and exciting team working on a global processes optimisation project, within the Innovation & Research division.  You are an outstanding IT professional with minimum 5 years' experience in: Project Management Business Process Reengineering Process Optimisation Digital Innovation Experience in data science and artificial intelligence topics is a plus.  You are a great team player and out of the box thinker, accustomed to working under pressure and in a challenging environment, with good problem solving capabilities.  Experience in the pharma/chemical sector and fluency in English complete the profile. Fluency in German and/or French is a great plus.  Workplace:  Basel city

PURPOSE OF POSITION Viking Cruises is one of the world’s leading cruise line company that manages a fleet of 72 river ships and 6 ocean ships (and growing) with offices across the globe. We have our Marketing and Sales headquarters based in Los Angeles, USA and the Operational Head Quarters based out of Basel, Switzerland. The Business Solution team (within IT) plays an integral role in the strategy, architecture, design/acquisition, implementation and management of various business applications and software solutions to enable planning, efficient operation, automation and reporting needs of the company. As a key member of the Business Solutions and IT Team, the Data Solutions Manager will provide solutions to our current data challenges and holds a key role in our technology modernization programs. S/He works on data technology and related innovation projects with a global reach and has a hands-on approach to understanding various data integration methods while paving the way for standards across the enterprise. The Data Solutions Manager reports to the Director Business Solutions. Starting date would be as soon as possible. This role will be located in Basel, Switzerland. Please note that we can only accept candidates who are eligible to work in Switzerland or are in possession of a relevant work permit. RESPONSIBILITIES Provides guidance, leadership and expertise to define the ‘data’ solution architecture and strategies across various departments throughout the enterprise. Leads and manage internal and external (3rd party developer) teams to execute multiple projects related to integration between systems, data warehouse, data governance and dashboard/report development. Develop architectural standards, workflows and interface specification documents that complement the architectural vision well enforcing best practices. Design and create the physical data model for the data warehouse by analyzing the data from all source system applications and/or from external sources. Ensuring reliable, accurate, and accessible data for responsible data entry areas Ensure existing data/information assets are identified, stewarded and leveraged across the enterprise Collaborate with the rest of the Business Solution team on relevant data tasks that are part of projects – related to ERP system, Office 365, SharePoint Online, etc. Educate team members and business partners on area of technical expertise Enable and empower business users and sponsors to access and consume data easily for maximum business benefit Optimizes the information technology solutions to the enterprise-wide system requirements of Viking Cruises QUALIFICATION PROFILE Bachelor’s degree or higher in Computer Science, information technology or a related field MCSD, MCSE Data Management and Analytics or similar certifications would be a plus. Certifications on Data Science or Big Data is also a plus Project Management Certification (PMP or PRINCE2) is a plus, but not required 3 - 4 years in a similar role Experience with Enterprise Data Architectures and building/managing data assets Experience with data integration, having done multiple ETL between systems. Data virtualization or replication experience is not required, but a plus Solid background in data management including big data technologies and data warehouse solutions Experience across all phases of data modeling, from conceptualization to database optimization and governance Experience working in a complex environment with multiple source systems feeding a data warehouse Experience in using some (if not all) of the Data Management tools like Microsoft SSMS to SSIS, SSDT/SSAS, SSRS, PowerBI and SQL are a must. Experience in use of any Big Data tools is a plus Experience in leveraging any of the Artificial Intelligence / Machine Learning tools to improve the data assets of a company is a plus Ability to provide direction, strategy and value by analyzing current and future states of data, setting and communicating standards, and conception of projects or features to close the gap between current state and future goals Great experience in business analysis - Ability to learn and understand complex processes, systems and data structures Ability to understand business requirements and manage priorities - Skills in creating well defined tasks from business requirements, having in mind its priority and complexity, as well as the impact on current system Fully engaged in the project, being responsible for managing requirements and its priorities, but also responsive for questions from development team Knowledge of dimensional modeling, data warehousing, data governance and Big Data concepts Build relationships with business stakeholders and partners to understand information needs Ability to work on multiple initiatives and work streams at one time in a global environment Quick learner with ability to pick up new technologies/skills and business knowledge Ability to show flexibility, initiative, and innovation when dealing with ambiguous and fast–paced situations Define enterprise information strategy and roadmap that aligns with corporate goals Deliver complex software systems through all phases of a software delivery lifecycle Ability to work on multiple projects running concurrently by leveraging scalable external teams Ability to capture, organize and analyze Big Data Passionate about DATA, DATA and DATA – which includes gathering, architecting, organizing, governing and visualizing data into meaningful information Ability to provide technology direction and setting standards for data platforms, involving all aspects of information access and retrieval, integration, middleware translators, utilities, tools, and languages for use by information technology groups. Ability to communicate the benefits and advocate the use of enterprise wide data architecture and standard platforms, products and tools to senior management, business area staff and technical staff Excellent analytical and problem solving skills with great interpersonal dispositions and communication skills Willing to work with various business team(s) and are comfortable, patient with varied stakeholder groups Excited about working in the cruise industry WHAT WE OFFER Flexible working hours On-site employee restaurant (including complementary soft drinks, coffee, tea) Regular company events, e.g. sports games, barbecue, cooking classes A dynamic and fast-growing environment where you can drive your future A free cruise for you and your +1 every two years A highly talented, passionate and international team If you are interested in this role, please apply via our website, including a cover letter (one page, introducing yourself and outlining why you are interested in the role) as well as your CV and relevant references.

The Position We're looking to hire a Scientific Marketing Specialist for an 80-100% permanent position in Basel. The role is broad but centered around producing and delivering marketing material to our target audience and managing brand communication. The position includes writing and maintaining presentations, brochures, website copy, and promotional emails, which requires native or near-native English proficiency and a keen eye for visual presentation. In addition, you will follow up and present the results of your work internally. As we move towards increasing marketing automation, your role will also come to include set-up and administration of our activities planned in this area. You will coordinate with the marketing, sales, and professional services teams to make sure that your activities and all other campaigns, messages, and events align. Your work, while internal, will constantly focus on customer needs and interest, so you should have or quickly gain an understanding of where our customers are and what they need from us, while also keeping your ears open to the needs of the internal organization. When you are not busy with your regular tasks you will have the opportunity to learn about and help us improve other areas in marketing, aligned with your interests and our needs. We are happy to teach you what we know and look forward to learning from you. To help us understand who you are and what motivates you, please include a paragraph on what sentence in this ad attracted you the most to this position, and why. Key Responsibilities Produce and maintain marketing collateral, including brochures, emails, and presentations Shape and own Screener’s website activities, including SEO-relevant copy Plan, execute, and follow up mailing and social media campaigns Handle advertisements and AdWords campaigns Update and use our CRM system to produce campaign statistics Later: Set up and administrate marketing automation activities Your Profile MSc in natural sciences 2 years’ experience in writing and preparing marketing/communications/sales materials Native or near-native English proficiency is required Experience in using PowerPoint to explain complex concepts Strong grasp of marketing and branding concepts, with experience in B2B marketing Highly organized and dedicated to quality of work Experience in Photoshop and InDesign with an eye for layout is a strong advantage Background in drug research and development The Company Genedata is an exceptional company. With over two decades of success in research informatics due to closely-knit teams of scientists, developers and business experts, Genedata has achieved steady and continuous growth since inception. As a private and majority employee-owned organization, we empower each employee to be a contributing voice in the company operations and evolution. Our collective expertise in research informatics, combined with our open and scalable computational solutions, makes us the leading software provider in R&D informatics for biotech, pharmaceuticals, and related life sciences. We are headquartered in Basel, Switzerland and have subsidiaries in Germany, US, UK, Japan and Singapore. About Genedata Screener® Genedata Screener® analyzes, visualizes, and manages screening data from in-vitro screening assay technologies across the enterprise, including very complex as well as ultra-high throughput experiments. Its screening-oriented business logic enables rapid processing and comprehensive analysis of complete campaigns. Are You Interested? If you are interested in this position, please submit us your CV and motivation letter. Genedata is an Equal Opportunity Employer. Genedata only accepts CVs and resumes directly from candidates. Personnel recruitment agencies need not respond.

The Position We are looking for a Scientific Consultant / Field Application Scientist for a full-time permanent position within our Genedata Screener business unit. The Scientific Consultant is a scientific and technical consultant for our customers. It a highly dynamic job – you will wear many different hats, interact with many different people, and use your scientific and technical knowledge to solve real-world scientific screening problems. This position is especially well suited for you if you have a scientific/technical background, enjoy variety in your daily work, and want to expand your skill set (scientific, technical, and soft skills). This full-time position is based in our headquarters in Basel, Switzerland and requires about 30% travel within Europe, and occasional travel to North America. Key Responsibilities First and foremost, you will become an expert in scientific and IT matters related to biological (small and large molecule) screening data analysis in general and the use of our Genedata Screener software in particular. You will combine this expertise with excellent communication skills and project management know-how to (a) support our customers in getting the most out of Genedata Screener, (b) aid our sales team, and (c) propose, plan, execute and manage projects. (a) You will establish relationships based on trust with our customers by being their first point of contact and sparring partner on scientific and technical matters. We want our customers to have excellent screening processes, and it will be your job to get them there. You will also provide user training and product support. (b) You will work in tandem with our Business Account Managers in establishing and communicating the value of Genedata Screener to prospects and customers. Tasks include qualifying customer needs, giving pre-sales presentations and demos, and managing software evaluation projects. (c) In addition, you will act as project manager for projects of different types: scientific consulting, software implementation, systems integration, and data analysis projects. You will ensure their delivery at the level of excellence that our customers know us for. This involves proper project set up and planning to achieve the customer’s goals; specifying and coordinating the implementation work of our developers; guaranteeing adherence to scope, budget and timelines; managing change in the project; controlling the quality of all deliverables; providing customer feedback to product management; and supporting the Screener team to keep improving our processes. In addition to the core responsibilities listed above, we want you to help all of us in the Screener team to improve, and we count on your knowledge, creativity, and technical skills to further advance our science, marketing, development, and product management. Your Profile Essential Skills and Experience: You will be exposed to a range of different people, so you should feel comfortable interacting with customers at all levels (managers, scientists, and IT experts) and be prepared to constantly communicate internally. We are particularly looking for candidates with a degree (preferably post-graduate) within quantitative biology, bioinformatics, applied physics, applied mathematics, or a related field. In addition, 2+ years of industry experience would be a definitive advantage, especially in a pharmaceutical or biotechnology company, a contract research organization, a consulting company, a provider of scientific software, or the software department of a provider of screening instrumentation. If you do not have experience in any of these companies, we look forward to receiving your application if you possess the skills listed below, are a fast learner and wish to quickly delve into the scientific and technical challenges of cutting-edge screening technologies in the context of Pharmaceutical R&D. Additional Preferred Skills and Experience: Technical skills: The role involves scripting and working with UNIX systems, which means that experience with at least one scripting language (preferably Python) as well as basic familiarity with the UNIX shell environment will get you up to speed faster. Familiarity with Java, networks, databases, data mining, image analysis, distributed systems, and/or web technologies is an advantage, but not strictly required for the job. Experience in managing IT projects involving multiple stakeholders is a clear plus. Industry knowledge: You will work with a range of screening technologies and application areas (please see our website for currently supported technologies), so deeper knowledge within a few or broader knowledge across several of them would be desirable Our customers are mainly pharmaceutical research organizations, thus your experience with pharmaceutical research and the drug discovery process would be valuable to us. The Company Genedata is an exceptional company. With over two decades of success in research informatics due to closely-knit teams of scientists, developers and business experts, Genedata has achieved steady and continuous growth since inception. As a private and majority employee-owned organization, we empower each employee to be a contributing voice in the company operations and evolution. Our collective expertise in research informatics, combined with our open and scalable computational solutions, makes us the leading software provider in R&D informatics for biotech, pharmaceuticals, and related life sciences. We are headquartered in Basel, Switzerland and have subsidiaries in Germany, US, UK, Japan and Singapore. About Genedata Screener Genedata Screener® analyzes, visualizes, and manages screening data from in-vitro screening assay technologies across the enterprise, including very complex as well as ultra-high throughput experiments. Its screening-oriented business logic enables rapid processing and comprehensive analysis of complete campaigns. Are you interested? If you are interested in this position, please submit us your CV and motivation letter. Genedata is an Equal Opportunity Employer. Genedata only accepts CVs and resumes directly from candidates. Personnel recruitment agencies need not respond.

Responsibilities: The Safety Research Scientist contributes to the development of new animal health products by providing strategic and scientific expertise for Safety programs that will meet global regulatory requirements, and provide an innovative approach to achieving Elanco R&D objectives. The purpose of this position is to manage the outsourcing of safety studies (target animal safety, toxicology and environmental safety) to Contract Research Organisations (CROs). As part of a Development Team, this position takes responsibility for the assessment and selection of CROs and for the design, outsourcing, conduct and completion of safety studies as well as for data assessment and interpretation. This role interacts with regulatory agencies globally and leads the effort to build the global safety dossier. Key Leadership Responsibilities: Work effectively and flexibly within and across all Elanco R&D teams and external collaborators to achieve overall Elanco R&D deliverables. Create a positive work environment that is aligned with company objectives. Create an engaging culture with a “Play to Win” mentality. Provide and accept challenge to deliver innovative technical solutions and create an innovative culture. Proactively search for solutions. Identify and utilize methods to deliver individual objectives in a high quality, timely, cost-effective manner. Provide information to facilitate accurate and timely project and budget forecasts. Manage project timeline and budget deliverables to facilitate delivery of the Elanco pipeline. Coach/support other colleagues for optimal project progress. Ensure efficient and open communication, and take lead to resolve conflicts. Key Technical Responsibilities: Assume overall responsibility and accountability for the Safety programs (target animal safety, toxicology and environmental safety) of a project Develop, update and implement project strategies to achieve objectives in the optimal timeline and budget, define and control achievement of critical project milestones, ensure critical issues are accurately addressed and resolved in a timely fashion. Plan, execute and report Safety studies (including but not limited to drafting protocols, data capture forms, data output, and reports; serving as study monitor or sponsor person responsible). Identify and select research facilities, establish contract agreements, maintain Sponsor Oversight and a positive business collaboration. Determine needs and procure necessary study supplies, including test articles, reference standards, and appropriate formulations for Safety studies. In collaboration with QA, ensure the quality and compliance of all development studies by conducting them according to the protocol and appropriate quality standards (GCP/GLP). Coordinate, supervise and/or conduct data management, pharmacokinetics, and statistics for Safety studies as necessary. Assume global responsibility and accountability for the Safety part of registration dossiers, which can include the preparation of the corresponding secondary documentation like Safety Experts Reports, User Safety Assessments, Environmental Risk Assessments in partnership with Elanco Regulatory for regulatory agencies globally. Attend meetings with regulatory agencies and present the safety plan, and respond to agency questions (verbally and in writing). Actively participate and contribute to Development team activities, meetings, project coordination, improvement of processes, etc. Prepare publications as needed in alignment with the Development team and Marketing. Provide technical support and/or guidance to other R&D teams as a Subject Matter Expert. Work with internal partners (i.e. TACs) to provide technical support to currently registered companion animal products. Company Overview Elanco Animal Health is a global animal health company that develops products and knowledge services to prevent and treat diseases in food animals and pets in more than 90 countries. Founded in 1954, we rigorously innovate to improve the health of animals and benefit our customers, while fostering an inclusive, cause-driven culture for more than 5,800 employees. Basic Qualifications University degree (Ph.D. in Biology/Chemistry or Doctorate of Veterinary Medicine (DVM) or related field) and broad experience in drug safety and a good background in regulatory requirements with 3+ years experience in the Veterinary or Human Pharmaceutical industry , or MS with broad experience in drug safety and a good background in regulatory requirements with 6+ years experience in the Veterinary or Human Pharmaceutical industry. Proven proficiency in global drug development e.g. Study or Program Design, FDA concurrence, product approvals. Demonstrated success in managing contractors and relationships with external parties. Additional Information Location: Basel, Switzerland Travel requirements: 10-20% Additional Skills/Preferences Board certification as toxicologist (DABT, ERT, ECVPT) is considered as an ideal additional asset. Exceptional problem solving and decision-making skills with the proven ability to think beyond a study outcome to a project/program outcome Knowledge of CM&C (chemistry, manufacturing and control), clinical trial design, pharmacokinetics and statistics Proven track record of designing and implementing safety programs from early development through registration/approval Must be able to work productively in an interdisciplinary and global team environment with the proven ability to communicate across multiple disciplines effectively Proven ability to interpret, discuss and present data in a clear, concise manner and provide recommendations at the project level Demonstrated proficiency of GLP/GCP and quality principles Advanced planning and tracking skills, capable of managing multiple projects with respect to priorities and self-management Proven “team player” mentality, with the goal of organizational success over individual success

Responsibilities: The Safety Research Scientist contributes to the development of new animal health products by providing strategic and scientific expertise for Safety programs that will meet global regulatory requirements, and provide an innovative approach to achieving Elanco R&D objectives. The purpose of this position is to manage the outsourcing of safety studies (target animal safety, toxicology and environmental safety) to Contract Research Organisations (CROs). As part of a Development Team, this position takes responsibility for the assessment and selection of CROs and for the design, outsourcing, conduct and completion of safety studies as well as for data assessment and interpretation. This role interacts with regulatory agencies globally and leads the effort to build the global safety dossier. Key Leadership Responsibilities: Work effectively and flexibly within and across all Elanco R&D teams and external collaborators to achieve overall Elanco R&D deliverables. Create a positive work environment that is aligned with company objectives. Create an engaging culture with a “Play to Win” mentality. Provide and accept challenge to deliver innovative technical solutions and create an innovative culture. Proactively search for solutions. Identify and utilize methods to deliver individual objectives in a high quality, timely, cost-effective manner. Provide information to facilitate accurate and timely project and budget forecasts. Manage project timeline and budget deliverables to facilitate delivery of the Elanco pipeline. Coach/support other colleagues for optimal project progress. Ensure efficient and open communication, and take lead to resolve conflicts. Key Technical Responsibilities: Assume overall responsibility and accountability for the Safety programs (target animal safety, toxicology and environmental safety) of a project Develop, update and implement project strategies to achieve objectives in the optimal timeline and budget, define and control achievement of critical project milestones, ensure critical issues are accurately addressed and resolved in a timely fashion. Plan, execute and report Safety studies (including but not limited to drafting protocols, data capture forms, data output, and reports; serving as study monitor or sponsor person responsible). Identify and select research facilities, establish contract agreements, maintain Sponsor Oversight and a positive business collaboration. Determine needs and procure necessary study supplies, including test articles, reference standards, and appropriate formulations for Safety studies. In collaboration with QA, ensure the quality and compliance of all development studies by conducting them according to the protocol and appropriate quality standards (GCP/GLP). Coordinate, supervise and/or conduct data management, pharmacokinetics, and statistics for Safety studies as necessary. Assume global responsibility and accountability for the Safety part of registration dossiers, which can include the preparation of the corresponding secondary documentation like Safety Experts Reports, User Safety Assessments, Environmental Risk Assessments in partnership with Elanco Regulatory for regulatory agencies globally. Attend meetings with regulatory agencies and present the safety plan, and respond to agency questions (verbally and in writing). Actively participate and contribute to Development team activities, meetings, project coordination, improvement of processes, etc. Prepare publications as needed in alignment with the Development team and Marketing. Provide technical support and/or guidance to other R&D teams as a Subject Matter Expert. Work with internal partners (i.e. TACs) to provide technical support to currently registered companion animal products. Company Overview Elanco Animal Health is a global animal health company that develops products and knowledge services to prevent and treat diseases in food animals and pets in more than 90 countries. Founded in 1954, we rigorously innovate to improve the health of animals and benefit our customers, while fostering an inclusive, cause-driven culture for more than 5,800 employees. Basic Qualifications University degree (Ph.D. in Biology/Chemistry or Doctorate of Veterinary Medicine (DVM) or related field) and broad experience in drug safety and a good background in regulatory requirements with 3+ years experience in the Veterinary or Human Pharmaceutical industry , or MS with broad experience in drug safety and a good background in regulatory requirements with 6+ years experience in the Veterinary or Human Pharmaceutical industry. Proven proficiency in global drug development e.g. Study or Program Design, FDA concurrence, product approvals. Demonstrated success in managing contractors and relationships with external parties. Additional Information Location: Basel, Switzerland Travel requirements: 10-20% Additional Skills/Preferences Board certification as toxicologist (DABT, ERT, ECVPT) is considered as an ideal additional asset. Exceptional problem solving and decision-making skills with the proven ability to think beyond a study outcome to a project/program outcome Knowledge of CM&C (chemistry, manufacturing and control), clinical trial design, pharmacokinetics and statistics Proven track record of designing and implementing safety programs from early development through registration/approval Must be able to work productively in an interdisciplinary and global team environment with the proven ability to communicate across multiple disciplines effectively Proven ability to interpret, discuss and present data in a clear, concise manner and provide recommendations at the project level Demonstrated proficiency of GLP/GCP and quality principles Advanced planning and tracking skills, capable of managing multiple projects with respect to priorities and self-management Proven “team player” mentality, with the goal of organizational success over individual success

Amaris is an independent, international Technologies and Management Consulting Group. Created in 2007, Amaris is already established in over 50 countries and supports more than 850 clients worldwide throughout their project's lifecycle. Our expertise covers five areas of innovation: Business and Management, Information Technologies, Engineering and High Technologies, Telecommunications and Biotech and Pharma. With more than 65 offices across the world, the Group offers proximity support to its clients in all their locations and many opportunities of international careers for employees. In 2019, Amaris aims to reach a turnover of 350 million euros, 6500 employees and to develop its workforces with the anticipation of a further 2000 new job openings. We expect to triple our workforce within the next few years and reach a leading international position in independent consulting.  Your Role  For one of our most important clients operating in the pharma/chemical sector, we are looking for IT consultants/managers experts in process optimisation and digitalisation.  The selected people will join a dynamic and exciting team working on a global processes optimisation project, within the Innovation & Research division.  You are an outstanding IT professional with minimum 5 years' experience in: Project Management Business Process Reengineering Process Optimisation Digital Innovation Experience in data science and artificial intelligence topics is a plus.  You are a great team player and out of the box thinker, accustomed to working under pressure and in a challenging environment, with good problem solving capabilities.  Experience in the pharma/chemical sector and fluency in English complete the profile. Fluency in German and/or French is a great plus.  Workplace:  Basel city

Our client, a market leader with a solid reputation in the Life Science industry, is looking to grow it’s presence and team in their office in Basel. Today it’s a small team, almost a start up in size, who are looking to grow by adding talented people like you! Passion, ambition and working together towards a common goal underline the mentality our client has and wants. With an international culture, but a business, an ethic and a focus on quality tailored to the Swiss market, our client is looking for you! Your abilities and mindset: First experience in recruitment, ideally in Life Sciences. Communicative, outgoing and passionate about recruitment. Service oriented, relationship driven and want to deliver high quality solutions and results. Able to work autonomously and like an entrepreneur. English is essential, German would be very nice to have. Your challenge: Sourcing, hunting, attracting, selecting and interviewing leading talent within the life science industry. Proactively build talent pipelines. Maintain databases quality to ensure all candidate data is captured and tracked. Responsibility of administrative activities such as candidate correspondence, creating & publishing jobs, interview planning and scheduling, assessment preparation and reporting. Delivering a positive candidate experience and acting as an ambassador. Your reward: The opportunity to be promoted quickly based on performance. One of the most attractive commission progammes in recruitment. The opportunity to continue your career in other countries if you wish to move abroad. Not a KPI focused environment. International client and candidate base. This is a unique chance to join a company where the start-up buzz and financial opportunity are amazing. Led by a competent and experienced manager, this is a great chance to really take your career to the next level. Curious? Get in touch and send us your CV to find out more.