Bayer job subsription

• Global steering of the Active Pharmaceutical Ingredients (API) supply mainly to the Product Supply Animal Health production sites with regard to strategic and technical aspects • API demand planning including starting materials and delivery tracking according QUOTIF KPIs (quality on time in full) • Consulting and providing technical support to the API manufacturing plants (mainly parasiticide plants initially at low Good Manufacturing Practice level) in order to fulfill the respective GMP and quality requirements • Following-up of audits by implementation of the required corrective actions and upgrade measures • Active contributions to R&D projects with regard to the supplier identification and qualification for new APIs • Management of cross-functional project teams in case of relocation of the API production • Strategic risk management for supervised APIs by risk analysis and implementation of measures for risk mitigation • Ensuring regulatory compliance of th

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As Director/Senior Pharmacometrics Strategist Women's Health/Gynecological Therapies (m/f) you will lead pharmacometrics activities in Strategist Women’s Health/Gynecological Therapies projects from preclinical development until life-cycle management. Your main responsibility is the systematic establishment and perpetuation of project specific pharmacometrics strategies in alignment with the respective project teams. You will have to specify the operational pharmacometrics work to be performed by our Quantitative Pharmacology departments. Your tasks will also include driving model based drug development strategies across projects within the therapeutic area Strategist Women’s Health/Gynecological Therapies in order to optimize prospective studies and to maximize the use of available data. Translating of pre-clinical into clinical models to establish a model continuum as well as ensuring and tracking timely conduct of pharmacometrics activities through the respective responsible departm

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Your task is to identify and evaluate techno-economic developments in the core markets of our Bayer internal and external clients. The research and analysis of technology trends, industry cost structures and value chains is part of your activity as well as the development of related strategic recommendations. You will be involved in consulting projects in close cooperation with our senior consultants. Furthermore you will support the methodological development of our consulting community.

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The Global Brand Manager Biologicals (m/f) develops global strategies and tactics for portfolio management including programs to expand the market for existing brand(s), launch plans for new brand(s)/line extensions, and support for brand management activities in the regions/countries. The field of responsibilities will be amongst others in the Brand Strategy, Segment insights, life cycle management (LCM), and key opinion leaders (KOL) management. This will include: • Developing and establishing strategic brand plans for the global business (B2B and/or B2C where applicable) that direct the allocation of global marketing resources and provide guidance to the countries • Setting objectives for market research on the biological segment, • Developing and updating international marketing tools (e.g. global detailers, advertising, PR and promotional activities etc.) and facilitating inter country exchange of best practice • Leading the LCM planning for the brands and maximizin

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In your new position you will develop and define sourcing strategies for Fabricated Equipment with regional focus on European suppliers in agreement with the Global Sub-Category Head for Fabricated Equipment. Furthermore, you will align the Europeanwith the global sourcing strategies, including further development of sourcing in low cost countries like India and China. Your role will encompass development of new suppliers including the optimization of the existing supplier portfolio. You will also procure “Fabricated Equipment” under own responsibility for global Bayer MaterialScience Capital Investment projects with regional focus on European suppliers as well as serve as Procurement Lead of “Fabricated Equipment” for the Capital Investments unit by integrating and coordinating all relevant projects according to the agreed sourcing strategies. Moreover, you will monitor supplier performance and workshop load in order to evaluate and control delivery schedules and quality in accordanc

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• Developing marketing strategy propositions and commercialization concepts for Global Cosmetics • Taking responsibility for existing and future Baycusan® C business in the regions EMEA and LATAM • Optimizing effectiveness and efficiency of existing and new commercialization activities for the Baycusan® C products such as product attractiveness, marketing instruments, market positioning, etc. • Determining future business opportunities in the cosmetics market by assessing and analyzing technical trends and developments as well as by conducting market research and market analysis • Developing new case and feasibility studies, new products alignments, commercialization possibilities, and commercialization initiatives (technology push and market pull) • Leading a functional team of sales force with responsibility for Cosmetics in EMEA and LATAM • Supporting the regional sales force in negotiations with customers and securing appropriate sales resources within the di

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In your new position you will contribute your knowledge in innovative statistical methods to the development of new drugs in the cardiovascular area. This includes the application of modern trial designs and testing strategies, supported by extensive simulations on our parallel computing facilities. As a Project Statistician (m/f) you will support the development projects from phase IIb until approval and represent statistics in discussions with health authorities. In this role you will be a member of a multidisciplinary team and the leader of the biostatistical project team comprising other statisticians and statistical programmers. Occasionally, you will fulfill the role of a Study Statistician (m/f) for complex trials.

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• Responsibility for sourcing processes according to Bayer HealthCare (BHC) standards for all services supplied by contract development or contract manufacturing suppliers for pharmaceutical development and manufacturing services • Leadingnegotiations with international suppliers for financial and contractual topics as well as defining financial frame of such contracts • Performing key supplier management and supplier development • Supporting the development of optimized supplier portfolios through product- and market knowledge and performing supplier evaluations and risk analysis • Leading make or buy decisions processes within BHC with a focus on pharmaceutical manufacturing services • Elaborating sourcing strategiesfor technology categories within the Finished Product sourcing area • Realizing and implementing regional and global synergies out of the services and products supplied by external contract development and manufacturing suppliers using the l

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In your new job you will work on a large range of different simulation methods used for environmental safety assessments of our plant protection products. You will be responsible for quantitative exposure and risk assessments applying environmental fate models in combination with mechanistic effect models. Thereby an area of special interest will be the use of geo-information systems (GIS) to assess risks on the exposure as well as the effect side. Your work will be done in interdisciplinary cooperation with internal and external teams. You will represent the company in meetings with authorities and within the scientific community, while becoming a recognized contact partner for academic institutions and/or contract research organizations will also be part of your daily business.

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• Responsible for supporting the Medical Affairs strategy for indications for pipelines or marketed products • Providing the medical strategy for Global Phase IV Medical Affairs • Planning and coordinating the design, conduct, analysis, reporting and publication of Hematology Global Phase IV Medical Affairs studies • Providing strategic review of Hematology premarketing and postmarketing studies • Ensuring that all regional studies are consistent with the agreed Global Medical strategy •Providing medical expertise and insight on commercial issues • Planning and conducting scientific advisory boards with key opinion leaders and external customers • Providing Medical Affairs input to Global Clinical Development programs • Establishing and leading Medical Affairs matrix teams for Global Brands in Hematology

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• In charge of complex processes in the OTC- and pharmaceutical area as well as of the overall fit of process cluster • Representing the link between the global senior business process owner and the implementation partner • Listing process requirements from the country’s point of view and harmonize with the global process • Carrying out and coordinating feasibility studies and checking implementation options together with the implementation partner • Coordinating a „Functional Design Document“ for process cluster • Defining the requirements together with the country representative and sign-off of the „Functional Design Document“ • Securing that the process is planned and implemented in coordination to other processes • “Challenging” the local business representatives regarding the necessity of individual requirements in the light of global standard and compliance guidelines and takes over the responsibility for a solution • Evaluating requirements by taking time

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In your new position you will establish transparent data management processes on global and local R&D projects in the innovation portfolio of Bayer Animal Health (BAH) especially regarding project key status parameters like KPIs, financial figures, and business cases. Furthermore, you will provide congruent and holistic analyses and reports on innovation portfolio across all project types and decision points which are relevant for the BAH Decision Committee. Additionally, you will manage the development of the next level PMO IT-System as well as improve and maintain the current data base systems in consideration of holistic project information. Therefore, you will develop and execute training concepts for the above mentioned system focusing on improvement of data quality and usage. Your role will encompass establishing and maintaining of international working relations to all relevant stakeholders such as project Management, global & local R&D project environment, global marketing, reg

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• Responsible for the conduct of GLP residue trials in Europe • Responsible for the GLP compliant reporting of the field part of residue trials in Europe • Provide regular seminars, as well as technical and GLP training of personnel involved in residue studies • Elaborate SOPs, optimize and maintain expertise in the conduct of residue trials • Regulary visits to BCS sites to monitor BCS internal staff in the field • Regulary visits of contract research organisations to monitor contracted residue studies • Support and follow up of the further development of the IT systems related to residue studies (involvement in IT project work)

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You will develop novel bioinformatics tools and/or innovatively utilize existing tools to build custom workflows or pipelines that maximize the bioinformatics contribution to R&D research goals. You will work in a team to optimize and enhance our bioinformatics capacity to identify relevant epigenetic mechanisms in plants. You will contribute to research projects by performing and optimizing bioinformatics analysis. Furthermore you will contribute to data and application optimization across local and global informatics infrastructure to achieve appropriate performance of data access and software application. This is a fixed-term contract initially for two years with the possibility of being extended for another year.

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• Planning the BCS Quality Management strategy and objectives on a global basis • Developing, implementing and continuously improving the global Quality Management System with focus on Risk Management • Ensuring compliance with legal, regulatory and BCS key requirements • Striving for Quality Excellence by developing and improving KPIs • Providing expertise for troubleshooting, guidance and assistance to the global organization • Building a global Quality Management network to ensure continuous improvement by initiating a feedback process on the existing regulations • Maintaining interfaces to QA/QC-functions and ensuring a common approach • Representing BCS interests in Bayer Holding communities and external associations • Providing leadership and strategic development to the Quality Management team • Promoting skills and talents to establish Quality Management as an area for personal development

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• Monitor, consolidate, analyze, evaluate, and visualize clinical study costs on a global scale • Identify and provide early warnings in case of deviations as well as show the impact on business • Build a competence center for handling and controlling external costs for clinical studies and assume responsibility for training of controllers in subsidiaries • Manage the budget/forecast process for clinical study costs • Take responsibility for the process of obtaining actual costs and insurecorrectness of accruals • Develop recommendations to global management e.g. study managers and facilitate decision making in order to adhere to business goals • Identify problems proactively and take appropriate actions to solve them

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• Leading the global project team and coordinating the task together with the program manager • Defining the project scope and project plan in close cooperation with the country organization regarding time- and budget planning • Supporting the local and country project manager throughout all project phases • Planning resources in close collaboration with the respective resources • Preparing and conducting local workshops as well as preparation of the project documentation • Schedulingand conducting project management meetings/project steering committee meetings • Coordinating trainings and Change Management activities • Preparing and managing quality and acceptance tests • Preparing the local organization for the operation ofthe system and for the coordination of support tasks (Release Management) • Managing and supporting status reports as well as participation in status meetings • Collaborating in a global/virtual project team with intensive work-related travel acti

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• Drive cost reduction opportunities related to best value countries and facilitate implementation • Drive special project as e.g. the risk mitigation process and supplier management for raw materials, special intermediates and active ingredients • Provide Operational Excellence (OE) support for direct materials with focus on efficient processes, OE at suppliers, best in class negotiation maps and strategies • Ensure close alignment of processes and projects with the country organizations e.g. India and China • Central contact person for procurement tools e.g. P4U, spend map, ProTrak • Develop and implement sourcing strategies for special technology driven projects • Negotiate technology driven contracts and supply agreements with special suppliers • Manage Key Performance Indicators and metrics for direct materials and support that annual objectives are met (e.g. project timelines, savings target) • Provide process expertise to global and regional sourcing initiatives • P

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Within the MA organization the Senior GHEOR Project Leader (m/f) is responsible for a main product or a group of products or indications within a therapeutic area. In that role she/he: • Is responsible for HEOR aspects for the product/indications covered • Provides guidance and coaching to contract agencies and to potential GHEOR team members to ensure high quality and timely deliverables • Leads the development and implementation of the value strategy • Works very closely with Market Access Strategy Leader to ensure a comprehensive high quality strategic approach and implementation • Ensures payer-oriented value-driven development plans • Drives throughout development and steering during Life-Cycle management the production of quality health economics and outcomes data/evidence that can differentiate BHC products and establish the company as a credible partner to Health Care Technology Assessment (HTA) agencies/reimbursement authorities and healthcare professionals

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In your new position you will be responsible for biomarker identification, validation and strategy to establish biomarker panels in collaboration with consortia e.g. for heart and renal failures to enable patient stratification as well as quantitative pharmacology based on pharmacodynamic biomarker in early clinical studies and allow internal decision making with a focus on cardiovascular projects. You will work closely with other Global Biomarker and Experimental Medicine departments to ensuretransfer of assays/technologies from research to clinical application including functional measurements. As a biomarker project leader (m/f) you will lead several biomarker projects and resume in this role technical, scientific, strategic and budgetary planning for the assigned biomarker projects in an independent and efficient manner. You will ensure that validated biomarker assays are fit for purpose for application in clinical studies. As a lab head (m/f) you will be responsible for successfu

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• Managing and steering cross-divisional international BHC expert groups (Communities of Practice) in the fields of Maintenance and Solids Manufacturing • Identifying, developing and implementing best-practice solutions for the areas mentioned above together with Communities of Practice • Improving utilization of technical, commercial and organizational best practice solutions • Exploring new technical areas

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You will quickly be given responsibility within such consulting projects and will soon be working independently on specific assignments. You will have direct contact to clients and other consultants – in Germany and/or abroad, depending on the project – and will receive good insight into various areas of the Bayer Group. You will acquire and develop the necessary consulting tools and methodology through systematic personnel development. Your work will contribute to shaping the continual development of a growing inhouse consulting organization. Your project assignments will be an excellent starting point for a subsequent management career in a line function within the Bayer Group.

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• Collaboration in a Private-Public-Partnership Project with Scientists from Key Regulatory Authorities, Health Technology Assessment Bodies, Academia and leading multinational Pharma Companies on the development of innovative study designs for drug development • Addressing operational aspects of conducting pragmatic and adaptive clinical trial designs pre-launch by developing a better understanding of how methodology and study designs developed and used mainly for post launch RE can be applied successfully to investigational (unlicensed) medicines • Contributing to development and application of a feasibility assessment framework and practical tools to assess new study design approaches • Conducting interviews with key internal stakeholders to assess the practical issues and potential solutions associated with the range of study design options • Distilling the insights gained, together with insights from literature review and potential third-party stakeholders

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The Environmental Safety Function of Bayer CropScience (Monheim, Germany) is seeking a highly motivated scientist (m/f) for an interdisciplinary team that generates and interprets the data that are required for the approval of plant protection products and help to demonstrate their safety. You will be responsible for a small team of experienced technicians, and will plan, perform and interpret experimental studies to elucidate the metabolic pathways and the behavior of our active substances in animals, plants or environmental matrices. The results of these studies support the safety assessments of Bayer CropScience products worldwide and become part of the registration dossier. You will work with 14C-labeled and non-labeled compounds in a GLP environment and will apply a range of analytical methods (radio-HPLC, radio-TLC, LC-MS). Close co-operation in cross-functional teams is required for the interpretation of the data and to ensure consistency in dietary and/or environmental safety

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• Work in a research laboratory in the field of cardiovascular diseases research • Support internal development projects • Planning, execution and evaluation of in vivo pharmacology for the study of cardiovascular diseases (heart failure, arrhythmia, thrombosis, pulmonary hypertension, chronic kidney diseases) • Participate in interdisciplinary teams and projects from target identification, target validation to optimization of substances and preclinical studies This position ist limited for 2 years.

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As a research scientist/team leader (m/f) in Structural Biology (protein crystallography) you will provide structural biology support to lead discovery and lead optimization projects in cardiovascular and oncology research at our Pharma Research Centers in Berlin and Wuppertal. You will be responsible for structure determination of protein-ligand complexes as well as fragment-based screening using crystallography and protein-based NMR spectroscopy. You will be working in a team of experienced structural biologists and be an integral part of the Lead Discovery Department in Berlin. Your assignments will also include close interactions with colleagues from other areas such as protein technology, computational chemistry and medicinal chemistry. The communication and discussion of your results within multi-disciplinary drug discovery teams will form a central part of your work.

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As a Project Manager (m/f) you will lead teams of consultants and will be in charge of consulting projects in the areas of production and supply chain management with a strong emphasis in Lean and Operational Excellence in chemical/pharmaceutical industry. You will acquire and develop the necessary consulting tools and methodology through systematic personnel development. Your project assignments will be an excellent starting point for a subsequent management career in line functions within theBayer Group.

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Within our Global Drug Discovery Parasiticides, you will lead, coordinate and align the early evaluation of in vivo efficacy of exploratory anthelmintics, ectoparasiticides and antiprotozoals. Identification of technical needs and implementation of new in vitro and in vivo models to supplement our discovery process will be one of your main tasks. You will take responsibility in evaluating the feasibility of drug candidates in close collaboration with the respective discovery laboratories. Moreover, you will work inter-disciplinary with screening commissions and project teams in the joint selection, biological assessment and chemical optimization of new chemical entities. As a Senior Scientist (m/f), you provide the ability to develop and execute comprehensive research plans and study protocols. Furthermore, you are experienced in setting-up and managing internal and external collaborations including co-operations with international contract research organizations, scientific labs and u

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In your new position you will be responsible for novel technology research and assay qualifications to enable patient stratification as well as quantitative pharmacology based on pharmacodynamic biomarker in early clinical studies and allow internaldecision making with a focus on oncological projects. You will work closely with other Global Biomarker and Experimental Medicine departments to ensure transfer of assays/technologies from research to clinical application. As a biomarker project leader (m/f) you will lead several biomarker projects and resume in this role technical, scientific, strategic and budgetary planning for the assigned biomarker projects in an independent and efficient manner. You will ensure that validated biomarker assays are fit for purpose for application in clinical studies. As a lab head (m/f) you will be responsible for successful coordination of all tasks related to efficiently running a lab. You will provide successful leadership to guide a team (technician

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As part of the Market Access organization you will be responsible for the HEOR aspects of a main product, a group of products, or indications within a therapeutic area. As such you will provide guidance and coaching to contract agencies and to potential GHEOR team members to ensure high quality and timely deliverables. Moreover, you will lead the development and implementation of the value strategy while working very closely with the Market Access Strategy Leader to ensure a comprehensive high quality strategic approach and implementation. Thus, you will ensure payer-oriented value-driven development plans as well as drive throughout development and steering, during Life-Cycle Management, the production of quality outcomes data evidence that can differentiate Bayer Pharma products and establish the company as a credible partner to Healthcare Technology Assessment (HTA) agencies, reimbursement authorities, and healthcare professionals. Furthermore, you will develop Global Value Dossiers

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In an innovative environment, we build on the skills of people who know where they are heading and on people with a flair for dealing with others. Joining this program within Bayer HealthCare Product Supply Pharma, you will be assigned across different manufacturing sites, comprising both pharmaceutical/technical and managerial job profiles. The 24-month program also includes an international assignment and training stations in different functions, such as production (Supply Center in Germany and abroad) and headquarters functions (contract manufacturing, supply chain management, quality assurance). Furthermore, you participate in management training modules and you are mentored by an experienced Bayer Senior Manager. Together with your mentor and the respective Human Resources Business Partner, you will identify individual career perspectives, exchange feedback on your performance and agree on development measures.

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This HR key position is part of the Bayer internal Center of Expertise Compensation (CoE) reporting to the Global Head of Compensation. Compensation is part of the CoE Compensation, Benefits and Mobility, reporting to the Global HR Head of Bayer. The position shall be located in the APAC Region. Regional responsibilities: • Consult countries on Bayer’s global compensation philosophy and compensation processes • Consult and support countries and business groups in all compensation topics and local country projects • Ensure that compensation policies and practices are in line with global guidance and local market needs • Run compensation projects with country HR • Lead the regional compensation expert community, foster exchange, organize and conduct regional compensation conferences and workshops • Guide and support the annual Merit Increase and STI cycle in APAC region • Participate in cross functional projects Global responsibilities: • Global process owner (m/f) for certa

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• Develop and document partnering strategy to meet assigned objectives in cooperation with management • Build and maintain an effective network in the Animal Health market by establishing regular contact with companies across the region or across the globe • Analyze competitive landscape in limited therapeutic areas • Prepare and coordinate preliminary assessments of external opportunities together with relevant functions • Coordinate execution of confidentiality agreements, material transfer agreements as appropriate • Act as “first filter” of incoming opportunities based on understanding of business needs • Negotiate basic terms of potential collaborations in cooperation with management • Assist in preparation of approval documents for global decision bodies • Negotiate full contractual agreement with partner • Summarize duties and responsibilities for the implementation of partnership via alliance management or other body and serve as ongoing internal champion

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• Responsibility for the technical reliability and the technical compliance of all electrical parts of the production plant • Responsible for the electrical safety in the production plant • Responsible for the compliance with industrial safety regulations • Responsibility for achieving the requested technical OEE und QHSE targets defined by global management • Execution of the defined maintenance strategy for the plant and responsibility for the management of maintenance and Capex budget of the plant • Coordination of the maintenance and inspection activities in the plant (optimization of necessary down time and production purposes) • Continuous improvement and optimization of the technical chemical engineering processes and the installed equipment • Management and coordination of technical projects in the plant • Supporting the purchase department in negotiating service agreements with external suppliers

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• Identify unmet needs and innovation impulses for defined target markets in the fields of building and construction • Assess and develop these into Bayer MaterialScience opportunities by means of a broad external validation regarding technologies and markets • Understand competitive solutions and conduct critical analysis of material properties • Determine risks of material changes for the value chain and barriers in the value chain as well as estimate switching costs • Analyze building requirements from Building Decision Makers and formulate integrated offers on basis of solutions from the Bayer’s EcoCommercial building network • Deliver structured hand-over of projects to the business unit’s technology department as well ascontinuous support during the prototype and commercialization phase

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In your new position you will lead a High Throughput Screening (HTS) Lab and supervise technical assistants. You will be responsible for internal planning and prioritisation of projects together with the team as well as for planning and execution ofinterdisciplinary lead structure identification and optimization with adjacent groups (Display Technologies, Analytical Biochemistry, Molecular Biology as well as Expression, Purification and Analytics). Furthermore, you will identify and establish relevant biochemical and cellbased assays for wellbased screenings and analyse and interprete High Throughput Screening data. Besides presenting screening data to other functions like pharmacology, pharmacokinetic and toxicology you will represent Global Biologics in interdisciplinary project teams.

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Your work will principally focus on Research & Development, however, other consulting projects might require your expertise. As a Project Manager (m/f) you will lead teams consisting of up to 4 consultants and will be responsible for the implementation and delivery of consulting projects focusing on Research & Development or given responsibility for aspects of such projects. Your work will focus on projects within the Bayer Group. You will have direct contact to clients and other consultants – in Germany and/or abroad, depending on the project – and will receive good insight into various areas of the Bayer Group. You will acquire and develop the necessary consulting tools and methodology through systematic personnel development. Your project assignments will be an excellent starting point for a subsequent management career in line functions within the Bayer Group.

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Within the global pricing function and as a core member of the Riociguat market access strategy team (MAST), you will contribute by driving the commercial value of Riociguat. This comprises the development of a global pricing & reimbursement (P&R) strategy - ready for launch - that allows brand value maximization with broad market access and desired reimbursement status. You will consolidate various functional, market access-related and product performance-related perspectives into one commercial pricing & reimbursement policy. This includes the globally binding brand floor price and country specific target prices ensuring limited value erosion, generic price erosion and international price referencing. Adjusting the price strategy over Riociguat’s (and potentially assigned further products) brand lifetime in both directions will also be a part of your assignments as well as the utilization of price increase opportunities and minimization of the economic risks from competitive brands,

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As Director/Senior Pharmacometrics Strategist Oncology (m/f) you will lead pharmacometrics activities in oncology projects from preclinical development until life-cycle management. Your main responsibility is the systematic establishment and perpetuation of project specific pharmacometrics strategies in alignment with the respective project teams. You will have to specify the operational pharmacometrics work to be performed by our Quantitative Pharmacology departments. Your tasks will also include driving model based drug development strategies across projects within the therapeutic area oncology in order to optimize prospective studies and to maximize the use of available data. Translating of pre-clinical into clinical models to establisha model continuum as well as ensuring and tracking timely conduct of pharmacometrics activities through the respective responsible departments as defined by the project specific pharmacometrics strategy are also in your accountability. In addition, y

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You will be responsible for the development and application of statistical methods on pharmaceutical and biological problems in such areas as pharmacokinetics, bridging and stratification. Your tasks could also include the application of statisticalapproaches to production and quality issues and the scientific refinement of the respective statistical methods. You will perform scientific analyses of the results and communicate these to the customer. You will also be responsible for supervising students and PhD candidates.

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In your new role you will be responsible for the regular customer communication within Bayer Business Services (BBS) organization. You will manage different escalation issues in the field of Finance and Accounting Shared Services (FASS) for AccountsPayables (AP), Value Added Tax (VAT), Vendor Master Data (VMD) and specific customer groups. Therefore, you are responsible for checking AP, VAT as well as VMD Key Performance Indicators regarding their plausibility. Above your tasks you will assistthe Controlling and Service Delivery Manager (SDM) with product cost and sales related measures as well as support the Bayer Business Services common strategy development for products and customer relations. In addition, you will define in cooperation with Business Steering the pricing for AP, VAT as well as VDM materials. Furthermore, you will support the budget process for BBS FASS as well as perform the sales activities (quotation preparation, regular sales reporting) for product, subgroup an

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As a (Senior) Consultant/Project Manager (m/f) you will take responsibility for delivering management consulting projects in the areas of Strategic Planning, Business Development, Marketing & Sales, Supply Chain Management, Manufacturing, Finance & Controlling or Human Resources in compliance with the defined project objectives, scope quality standards, and resource budget. You will lead small project teams, serve as a coach and develop junior consultants in project work to improve their professional competencies. Your project assignments will be an excellent starting point for a subsequent management career in line functions within the Bayer Group. In addition, you will promote the services of Business Consulting to its clients, e.g. project proposal development, marketing activities or client relationship development and contribute to the overall development of Business Consulting globally concerning knowledge development, training, recruiting or internal event organization.

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• Develop in depth understanding of transportation market, customers, application needs, industry and segment data as well as competitors activities by collecting and interpreting market intelligence through industry and customer visits or events, exhibitions, associations, desktop research, and market research • Conduct industrial marketing process related to segmentation, targeting, positioning, value proposition, and offering for the respective segment • Work with sales organization on segment marketing concepts to protect and grow existing business and extract maximum value • Develop the marketing mix, value propositions, universal offering packages as well as the right positioning to ensure maximum value extraction • Design regional industry marketing communication concepts for the respective industry aligned with controlling and communications • Ensure the successful coordination and information sharing with marketing counterparts and the wider organization in

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• Project management of R&D projects • Project management of customer projects • Competence development in chemical reaction technology in alignment with competence development task of the group • Performing scientific work in the area of chemical reaction technology • Managing customer relations • Performing experiments at bench and lab scale, leading lab personal on project basis

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• Supporting the development and implementation of consistent and efficient processes (e.g. deviation / change management) at the Elberfeld manufacturing site for Large Molecules • Applying state-of-the-art Quality-Assurance-principles • Improving and maintaining compliant quality standards for manufacturing of Biologics (APIs, Drug Product) • Supporting of multidisciplinary team in GMP relevant aspects including review and approval of documents related to qualification and validation (production and quality) • Release or rejection of raw materials and intermediates for Biologics (APIs/Drug Product) to ensure consistent quality and compliance using SAP • Performing Quality Assurance-Oversight of all GMP relevant aspects of Biologics manufacturing operations including Batch record review and approval of Master Batch Records • Assessing, approving or rejecting of changes, deviations/complaints, qualification, validation or verification plans and records to ensure

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• Develop and implement sourcing strategies for global products of high strategic relevance • Ensure adequate assessment of market requirements, market trends and the technological capabilities of suppliers including the identification of cost reduction opportunities and facilitate implementation • Contribute to the management of Key Performance Indicators (KPIs) and metrics for the specific sourcing category • Develop and negotiate global contracts and supply agreements with key suppliers • Participate in global and regional sourcing initiatives and provide early information about essential global sourcing initiatives • Initiate and drive close communication and alignment with business partners/stakeholders • Accountable to demand owners and act as business interface for demand owners in alignment with strategic sourcing • Provide functional professional guidance and sourcing experience to colleagues

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• Developing and leading a strategic sourcing team • Fully realizing procurement synergies across global HealthCare, other Bayer Group Companies or other external partners • Acting as a team lead for strategic sourcing initiatives and maintaining liaison with business stakeholders • Developing the sourcing function to be the partner of choice for selection of indirect goods and services • Leading the development and execution of sourcing strategies to leverage Bayer HealthCare's buying power • Developing supplier relationships, which fundamentally improve Bayer HealthCare's cost structure • Assuring continuous supply of indirect goods and services to BHC globally at best conditions by implementing strategic portfolio management • Leading global cost reduction programs, coordinating requirements and objectives with the Bayer HealthCare stakeholders and supporting Procurement Community initiatives • Developing and preparing Supply Agreements and Long Term Contracts with

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In your new position you will work on controlling and/or accounting projects within the Bayer Group, which might also include other areas of consulting. According to that you will also have direct contact to clients and other consultants – in Germany and/or abroad, depending on the project – and will gain a good insight into various areas of the Bayer Group. You will develop the necessary consulting tools and acquire methodologies through systematic personnel development. Furthermore, your workwill contribute to shaping the continual development of a growing inhouse consulting organization. Your project assignments will be an excellent starting point for a subsequent management career in line functions within the Bayer Group.

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As Global Drug Safety (GDS) Data Analyst (m/f) you will support the Global Data Safety System Manager among others in creating query requests and criteria as well as maintenance of the GDS intranet portal. You will retrieve data and develop outputs from global pharmacovigilance and regulatory affair database to support analyses of drug safety related tasks in GDS and generate aggregat reports as well as other evaluations for submissions to regulatory authorities and internal use (e.g. quality management or management reports). Furthermore, you will perform workflow and data checks on the global pharmacovigilance and regulatory affair database, identify errors/inconsistencies in outputs, and resolve or escalate them to GDS System Manager orothers for further action. Finally, you will support the drug safety users in issues within single case processing or aggregate reporting.

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You will be responsible for a molecular biology laboratory within Biologics Research. In this context you will design, generate and test protein-engineering and antibody libraries in Bayer HealthCare’s state of the art antibody discovery and proteinoptimization expertise center in Cologne, Germany. You will evaluate new technologies, guide technical staff in molecular-biological assignments and work in close collaboration with scientists within the department and across Bayer to drive our portfolio of product-oriented research programs. You will represent Biologics Research within cross-disciplinary teams that propose and supervise therapeutic and other research projects.

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• Developing and leading the global training function for Bayer Pharma • Ensuring that the organization continuously delivers best-in-class trainings for marketers and commercial field force people by implementing global training standards at Bayer Pharma, with a strong focus on launch preparation • Counseling local and brand team training functions on hiring, assessing and developing their training managers and instructors • Introducing train the trainer measures • Driving usage of state-of-the-art training methods and assess the delivered materials against best-in-industry standards • Developing and implementing role specific curricula for marketers and sales people, aligned with existing Bayer competency guides, training offerings and talent management concepts • Working in close cooperation with global HR functions and key markets • Building the programs with internal and external partners in order to attract, develop and retain the most skilled marketers and sa

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Your role in the Business Consulting unit will essentially comprise supporting the consultants in their current projects. Depending on your qualifications and interests, your duties may range from data analysis, support at meetings and workshops, and assisting with project-related activities to assuming project responsibilities of your own. Within the projects, you will be in direct contact with customers and fellow consultants. You will gain interesting and challenging insights into the Inhouse Consulting activities of a DAX company.

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In your new position you will support the Polyurethanes Business Unit (PUR) to understand the automotive and transportation industry in terms of technology roadmaps and trends. You will assess competitive solutions together with the technical department to support converting unmet needs into PUR solutions and business as well as help to extract additional value for Bayer MaterialScience. Therefore, you will deeply understand and analyze the industry and customer’s technology, especially the application development, by building respective external expert network relationships. Furthermore, you will identify long-term strategic technical development needs for the transportation industry in cooperation with the sales team, by taking into consideration the application life-cycles and potential disruptive technologies. Besides, you will drive the assessment and validation of industry opportunities with high market attractiveness where probability of technical success is yet uncertain. Final

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In your new role within Global Market Research you will provide relevant and actionable market and customer insights to support one of our major Global Brand Teams with business recommendations based on primary and secondary market research. You will be responsible for the design and execution of international primary market research studies. You will guide, perform and interpret statistical analyses from which you will derive clear strategic business recommendations. You will be responsible for creating, analyzing, and interpreting secondary data reports on assigned products in order to provide an unbiased, in-depth understanding of our markets. Moreover, you will support major projects focusing on scope and opportunities of the market, segmentation, customer portraying, and patient journeys. Part of your responsibilities will be the identification of market research information needs, both collaboratively with internal business partners and proactively based on knowledge of market an

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Ensuring the timely and correct creation of clinical study reports for Phase 1/2a studies as well as of submission documents in cooperation with the Clinical Sciences' project leaders and study managers in accordance to the agreed submission relevant project-/study goals and abiding by all international and regulatory standards. This position is limited for two years.

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You will guide a team of life science technicians to evaluate and develop pharmaceutical compounds in ophthalmology indications and thus you will be responsible for the identification of novel opportunities in drug discovery. Moreover, you will leadinterdisciplinary project teams of colleagues from Pharmacology, Medicinal Chemistry, Drug Metabolism and Pharmacokinetics, Drug Safety Clinical Pharmacology and Development. Furthermore, you will take initiative to assist marketing in assessing opportunities. You will support and collaborate with other R&D functions including formulation, production and regulatory affairs. Based on your background, you will maintain and extend an international network with outside research and medical experts.In addition, you will assume responsibility for compliance with legal requirements of experimental life science research.

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Your work will principally focus on Procurement projects, however, other consulting projects might require your expertise. As a Project Manager (m/f) you will lead teams consisting of up to 4 consultants, being responsible for the implementation anddelivery of consulting projects. Your work will focus on projects within the Bayer Group. You will have direct contact to clients and other consultants – in Germany and/or abroad, depending on the project – and will receive good insight into variousareas of the Bayer Group. You will acquire and develop the necessary consulting tools and methodology through systematic personnel development. Your project assignments will be an excellent starting point for a subsequent management career in line functions within the Bayer Group.

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• Defining global CRM related processes and serving as an SME within CRM implementation projects • Gathering the process requirements in CRM program, estimating them in the context of globally defined processes • Serving as the connection between the business stakeholders and the technical implementation team • Consulting local organization of how to use new processes and how to adjust the local organization in order to be prepared to use new processes (change management) • Supporting pre-studies as a process expert

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• Managing lead generation and optimization projects across divisional units and sites, hit to lead process, considering biological, pharmacokinetic and toxicological results • In-licensing: Evaluation of in-licensing candidates and technologies • Feasibility evaluation of chemical synthesis for chemical development • Scientific evaluation of patents • Controlling of chemistry-related cost per project

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You will be given the opportunity to write your master thesis in the area of Technical Operations/Supply Chain Management and/or support consulting projects in the same functional area. The focus will be on the development and implementation of holistic operational excellence, lean production and supply chain management concepts for the life science industry, e.g. developing an end-to-end supply chain strategy, developing a lean transformation concept for global production centers, etc. Depending on your qualifications and interests, your duties may range from data analysis, support at meetings and workshops, and assisting with project-related activities to assuming project responsibilities of your own. Within the projects, you will be in direct contact with customers and fellow consultants. You will gain interesting and challenging insights into the inhouse consulting activities of a DAX company.

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Your work will focus on organizational development/change management and/or strategic HR projects, but you should also be interested in other aspects of consulting. As a Project Manager (m/f) you will lead teams consisting of up to 4 consultants. You will have direct contact to clients and other consultants – in Germany and/or abroad, depending on the project – and will receive good insight into various areas of the Bayer Group. You will acquire and develop the necessary consulting tools and methodology through systematic personnel development. Your project assignments will be an excellent starting point for a subsequent management career in line functions within the Bayer Group.

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• Advanced disease biology understanding and target identification in cardiovascular diseases from a genetic/genomic perspective • Providing/developing statistical methods for genome-wide association studies (GWAS), next generation sequencing and gene expression data analysis • Providing technical knowledge about processes for validating gene candidates as functional targets for therapeutic intervention • Working closely with internal cardiology research (Heart Diseases, Vascular Diseases, Kidney Diseases, Acute Care & Hematology) and clinical science teams to guide cardio-genomic projects • Collaborating with local, national and international research networks

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You will work as a Postdoc (m/f) within a multidisciplinary project team drawn from Synthetic Organic Chemistry as well as Biology, Biochemistry and Molecular Modelling in the field of crop science research. You will be responsible for the conception, the synthesis and optimization of lead structures, leading to the development of new, innovative crop protection products for biological testing. You will receive scientific and administrative support from the expertise and instrumental resources of a research-driven world-leader in crop science. This is a fixed-term contract initially for one year with the possibility of extention to a second year.

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In your new job you will work on a large range of different simulation methods used for environmental safety assessments of our plant protection products. You will be responsible for quantitative exposure and risk assessments applying environmental fate models in combination with mechanistic effect models. This will include the development and use of different kinds of population models for terrestric and aquatic species and the application of biostatistical methods to the evaluation of ecotoxicological tests. Your work will be done in interdisciplinary cooperation with internal and external teams. You will represent the company in meetings with authorities and within the scientific community, while becoming a recognized contact partner for academic institutions and/or contract research organizations will also be part of your daily business.

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As an expert (m/f) in Clinical Development of Food Animal Products (FAP), your main tasks will be leadership as well as development and execution of comprehensive plans in clinical development for livestock products. You will be responsible for the planning, organization, contracting, coordination, supervision, reviewing, evaluation and authorization of clinical efficacy and safety studies. You will prepare clinical development plans, submissions (Part 4) to regulatory agencies, applicant summaries and coordinate contributions of external clinical experts. Furthermore, you will be responsible for answering clinical questions from authorities on licensed products. During the licensing procedure, you will support global and regional marketing to achieve an optimal rollout and sale of FAP products by pro-active support of launch activities with e.g. publications, congress presentations or sale’s representative trainings. In addition, you will provide clinical contributions for product PSU

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As a Project Manager (m/f) you will lead teams consisting of up to 4 consultants. Responsibility within our projects will depend on your experience and qualifications. Your work will focus on projects within the Bayer Group. You will have direct contact to clients and other consultants – in Germany and/or abroad, depending on the project – and will receive good insight into various areas of the Bayer Group. You will acquire and develop the necessary consulting tools and methodology through systematic personnel development. Your project assignments will be an excellent starting point for a subsequent management career in line functions within the Bayer Group.

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Your tasks at Bayer Technology Services GmbH will lie in the design and creation of mechanistic models in the areas of pharmacokinetics and pharmacodynamics. You will also provide consulting to customers from pharmaceutical research and development on computational life sciences. You will also be responsible for the scientific analysis of the results and their communication to the customer.

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Your role in the Business Consulting unit will essentially comprise supporting the consultants in their current projects. Depending on your qualifications and interests, your duties may range from data analysis, support at meetings and workshops, and assisting with project-related activities to assuming project responsibilities of your own. Within the projects, you will be in direct contact with customers and fellow consultants. You will gain interesting and challenging insights into the Inhouse Consulting activities of a DAX company.

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In your new position you will lead the Global Clinical Development (GCD) Team, a cross functional, multinational team of internal experts, through clinical phase II – III trials, global product registration, and ICMP trials supporting product life cycle optimization. You will represent GCD as a member of the Global Project Team and Global Brand Team and prepare the Clinical Development Plan (CDP) in consultation with relevant key disciplines, including an operational plan with high level resource planning (timelines, budget and manpower). Furthermore, you will be responsible for the ongoing risk-benefit assessment of a compound until approval in a main country. The communication of medical project and study strategy, study results and clinical project results to internal and external bodies is in your accountability. Moreover, you will define the strategic approach and manage preparation of medical sections of key regulatory documents and provide medical expertise to Global Strategic M

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You will join Bayer via our trainee program or, if applicable, via an on-the-job training in preparation for your later employment in one of the functions Controlling, Accounting, Finance or Corporate Auditing. From the beginning and during your employment in our headquarters and our foreign subsidiaries you will take over challenging tasks in exciting fields of activity. You will establish your network in the global Bayer organization and gather valuable practical experience in an international company.

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• Develop, define and document partnering strategy and search priorities together with the Animal Health division as well as lead activities to achieve strategic objectives • Build on already established network and maintain regular contact withcompanies across the globe for projects of interest, checking availability of opportunities and promoting partnerships with BHC • Collaborate and drive decision-making regarding specific BD opportunities with internal stakeholders and external partners • Present project for approvals to global decision bodies, managing key stakeholders in order to gain support for project • Negotiate full contractual agreement with partner together with legal and present project for final approval, managing key HQ stakeholders in order to gain support for the project • Summarize duties and responsibilities for the implementation of partnership via Alliance Management or other appropriate group and serve as ongoing internal champion

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• Leading biomarker projects for one or more cardiovascular/haematological development programs and resume technical, scientific, strategic and budgetary planning • Acting, if nominated, as Clinical Pharmacology Leader (CPL) (m/f) or Early Clinical Leader (ECL) (m/f) to lead the global Clinical Science (CS) team and independently create, update and implement the CS project plan • Providing scientific expertise on biomarkers, companion diagnostics and personalized medicine to support internal decision making and patient stratification • Developing biomarker strategies independently and maintaining excellent working relationships with Biosample Management, CPL, ECL, Global Clinical Leader (GCL) and business unit (BU) representatives • Implementing biomarker strategies for concrete projects in clinical studies, writing and taking responsibility for biomarker sections in Clinical Protocols, Investigator Brochures, Master Plans, Clinical Study Reports and stand-alon

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Within Bayer’s international headquarters, located in Leverkusen near Cologne, we have an opportunity for a suitably qualified and experienced HR Specialist (m/f) to join our team. You will be responsible for providing a proactive and high quality HR administrative support with reliable and timely advice to our Italian based staff and managers for all HR enquiries. Furthermore, you will take care of different administrative HR processes such as Separation, Training and Compensation & Benefits. Initially, this is a fixed-term contract for one year.

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We offer internships and research projects within our interdisciplinary group “Systems Biology and Computational Solutions“ at Bayer Technology Services GmbH. You will work in a team on mechanistic modeling and its application in the pharmaceutical and biotechnological area. Your work may contribute to both internal R&D projects with a methodological focus or to application projects for our partners in the pharmaceutical and biotech industries, respectively. Your tasks will include modeling andsimulation of biological processes as well as development of new computational methods. Job opportunities with a more mathematical focus involve statistical modeling such as artificial neural networks, kernel machines or hybrid models are also available.

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