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Teva Pharmaceuticals
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  • The opportunityAs Senior Director, Global Product Strategy – Immunolog... Read More
    The opportunityAs Senior Director, Global Product Strategy – Immunology Early Pipeline - you will define the long-term strategic vision, and lead the global product strategy for Teva’s early-stage immunology pipeline - translating scientific innovation into long-term brand and business value. This key global leadership role is responsible for identifying disease areas and commercial opportunities for our early pipeline assets (Discovery to Ph2), as well as assessing external opportunities that could be licensed or acquired by Teva. You will collaborate closely with R&D, Business Development, Medical Affairs, and regional commercial teams to ensure early commercial input drives long-term value creation.  This position can be based in the US (Parsippany), the Netherlands (Haarlem) or the UK. (In the UK, it can be based remotely.)  TRAVEL REQUIREMENTS Approximately up to 20% travel to support key meetings and cross-functional planning. How you’ll spend your day Strategic Leadership: Develop and refine global commercial strategies for early-stage immunology assets aligned with Teva’s long-term portfolio vision.  Early Asset Development: Shape Target Product Profiles (TPPs), indication prioritization, and clinical endpoints to optimize future commercial success.  Business Development Support: Partner with BD teams to evaluate external opportunities, lead commercial due diligence, and inform licensing or acquisition decisions.  Market & Competitive Insight: Conduct early market assessments, unmet need analyses, and scenario planning to identify opportunities and risks.  Cross-Functional Collaboration: Ensure early commercial input informs R&D, Medical, Market Access, and Regulatory strategies.  Forecasting & Planning: Build long-range forecasts and strategic models to guide investment and governance decisions.  External Engagement: Partner with KOLs, advocacy groups, and external experts to validate assumptions and shape early strategic direction.  Your experience and qualifications Bachelor’s degree required; Master’s or advanced degree preferred.  A minimum of 15 years in the pharmaceutical or life sciences industry, with a minimum of 10 years in commercial or marketing leadership roles.  Proven experience with pipeline strategy, early asset development, or business development.  Strong understanding of immunology (experience across multiple therapeutic areas a plus).  Demonstrated ability to translate science into strategy and drive cross-functional alignment.  Strategic thinker with exceptional analytical, communication, and leadership skills.  Experience in Insights or Analytics is advantageous.  Read Less
  • The opportunityAs Senior Director, Global Product Strategy - Emrusolmi... Read More
    The opportunityAs Senior Director, Global Product Strategy - Emrusolmin & portfolio - you will define the long-term strategic vision and lead the global product strategy for Emrusolmin (and other global assets) - translating scientific innovation into long-term brand and business value. This key global leadership role is responsible for shaping and executing the brand’s strategic direction, driving launch excellence, and maximizing long-term value across key markets. You will collaborate cross-functionally to translate scientific innovation into compelling commercial strategies, ensuring success throughout its lifecycle.  This position can be based in the US (Parsippany), the Netherlands (Haarlem) or the UK. (In the UK, it can be based remotely.) TRAVEL REQUIREMENTS Approximately up to 20% travel to support key meetings and cross-functional planning. How you’ll spend your day Lead the development and execution of the global launch and brand strategy for Emrusolmin, including lifecycle planning and indication sequencing.  Align global forecasts, target product profiles (TPPs), and clinical endpoints to ensure strategic and commercial coherence.  Translate clinical and scientific data into differentiated value propositions and messaging to unlock reimbursement and drive early patient access.  Provide strategic leadership for additional assets within the global neurology portfolio.  Drive global launch readiness in partnership with regional commercial, medical, and affiliate teams.  Identify and prioritize market expansion opportunities, including new geographies and indications.  Guide lifecycle planning to optimize long-term brand value.  Collaborate with R&D, Medical Affairs, Market Access, and regional teams to inform evidence generation and asset decisions.  Oversee market insights, competitive intelligence, and KPI tracking to inform strategy and adapt plans.  Engage KOLs, advocacy groups, and external stakeholders to shape brand perception and support scientific exchange.  Own the global brand campaign and core messaging for Emrusolmin, ensuring consistency and relevance across markets.  Drive storytelling excellence to communicate Emrusolmin’s value to HCPs, payers, and patients.  Your experience and qualifications Bachelor’s degree required; Master’s or other advanced degree preferred.  Minimum 15 years of experience in commercial, marketing, or sales leadership, including significant people leadership.  Proven success in developing strategies that deliver long-term commercial results.  Recent experience in a Tier 1 market (US or EU5) preferred, ideally within the last 5 years.  Launch leadership experience, including collaboration with global functions (R&D, Medical, HEOR).  Experience across multiple therapeutic areas; neurology and/or rare diseases preferred.  Strategic thinker with deep knowledge of industry best practices and current market trends.  Recognized expert with strong leadership and communication capabilities.  Demonstrated success in developing others and leading high-performing teams.  Operates with autonomy and accountability in a global matrix environment.  Read Less
  • Senior Manager, Medical Operations Excellence  

    - Harlow
    The opportunityAs a key member of the medical Affairs Team, we are see... Read More
    The opportunityAs a key member of the medical Affairs Team, we are seeking a dynamic Senior Manager, Medical Operations Excellence to join our UK & IE Medical Affairs organisation. This pivotal role offers the opportunity to ensure operational excellence, support key strategic initiatives, and make a meaningful impact on patient outcomes through effective medical operations management.  Success in this role will be measured by:  Demonstrable improvements in process efficiency Stakeholder satisfaction with medical operations On-time project delivery Proactive identification of operational risks A day in the life of a Senior Manager, Medical Operations Excellence... Process Optimisation & Continuous Improvement Leadership Lead data-driven process transformation utilising Lean, Six Sigma, or structured improvement frameworks to deliver measurable efficiency gains and cost reductions Conduct comprehensive process analysis including current-state mapping, root cause analysis, stakeholder journey mapping, and quantitative measurement to identify opportunities and establish baseline metrics Design and implement future-state processes with demonstrable track record of achieving specific outcomes (cycle time reduction, error reduction, satisfaction increases) through collaborative cross-functional redesign Project Tracking & Performance Management Leadership Manage project portfolio oversight using advanced tools (M365 Loop, Planner, SharePoint) to track multi-workstream initiatives, dependencies, resource allocation, and critical milestones across Medical Affairs operations Develop dynamic project dashboards providing real-time visibility into project health, budget utilisation, timeline adherence, and resource constraints with automated alerts for variance and risk indicators Medical KPI Tracking & Performance Management Oversee multi-level KPI performance across MSL quantitative/qualitative metrics, training indicators, and medical brand plan measures through automated tracking systems and performance dashboards Foster accountability by partnering with MSL Managers and Therapy Area Leads to set targets, monitor progress, and implement corrective actions for performance deviations Monthly Reporting & Communications Management Produce comprehensive monthly reports consolidating budget performance, MSL field activity metrics, brand and therapy area insights, and medical information trends into executive-ready analytics and recommendations Develop integrated reporting frameworks that synthesise cross-functional data into actionable insights, highlighting performance against targets, emerging trends, and strategic implications for leadership decision-making  Monthly and Quarterly Budget Tracking Manage proactive budget oversight through systematic monitoring, variance analysis, and trend identification, linking financial performance to KPIs and project delivery milestones Manage stakeholder budget accountability by conducting monthly tracking meetings with Therapy Area Leads, addressing variances, and ensuring alignment between spend and strategic priorities  Medical Affairs Brand Plan Orchestration & Performance Management Partner with Therapy Area Leads to translate brand strategies into operational roadmaps with defined milestones, resource requirements, and success metrics across the medical affairs portfolio Establish monitoring frameworks with therapy area-specific KPIs and progress tracking systems that provide real-time visibility into strategic delivery and execution gaps Medical Affairs Capability Mapping, Development & Tracking Conduct capability assessments across Medical Affairs teams to identify skill gaps, competency levels, and development needs aligned to strategic objectives Design development programs including training plans and skill-building initiatives to address gaps and enhance team performance Your experience and qualifications Do you have...? Bachelor’s degree in business administration, Operations Management, Engineering, Life Sciences, or related analytical discipline Professional project management certification (PMP, PRINCE2, Agile/Scrum Master) or equivalent demonstrated competency (Highly Desirable) Master’s degree in business administration (MBA), Operations Management, or Process Improvement and/or process improvement certification (Lean Six Sigma Green Belt/Black Belt, Lean Management, Change Management) Extensive experience of managing strategic plan execution across multiple functions with demonstrated ability to translate strategies into operational roadmaps and tracking systems Proven stakeholder accountability management ensuring senior stakeholders’ responsibility for delivery while maintaining productive relationships and managing competing priorities Process improvement expertise with track record of facilitating cross-functional redesign, managing resistance, and implementing changes that delivered measurable outcomes (cycle time reduction, error reduction, satisfaction increases) Process improvement methodology proficiency in Lean, Six Sigma, or structured frameworks with ability to translate complex regulatory/compliance requirements into streamlined workflows Advanced project management capabilities including expert proficiency in tools (Loop, Planner, SharePoint), tracking multi-workstream initiatives, dependencies, and resource allocation with custom reporting and automated workflows Proactive risk identification and intervention with demonstrated ability to identify project risks, performance gaps, and budget/performance disconnects 2-3 months before critical issues Regulatory project experience managing projects with compliance timelines and successfully recovering troubled projects through proactive intervention Governance and monitoring expertise developing RACI matrices, dynamic dashboards, structured governance, and integrating project tracking with budget oversight Predictive analysis capabilities using systematic monitoring to identify opportunities proactively rather than reactive problem-solving Diverse experience valued: We recognise that relevant experience may come from various sectors including healthcare, manufacturing, technology, consulting, or public sector operations

    Are you...? Open to feedback and continuous learning Willing to adapt approaches based on evidence and stakeholder feedback Able to exhibit collaborative leadership style with ability to influence Able to think outside the box while maintaining regulatory compliance Proactive Good communicator Enjoy a more rewarding choice We support our people through every stage of their journey with us. Our flexible reward platform puts you in control, empowering you to tailor your benefits to fit your lifestyle, priorities, and what matters most to you. With 25 days of annual leave that grows with your service, the flexibility to purchase additional days, and two dedicated volunteering days each year, your time off is truly yours to enjoy, recharge, and give back. We prioritise your health with private medical insurance, life assurance, critical illness cover, and income protection. Whether you're growing your family or pursuing new adventures, our enhanced maternity and paternity leave, sabbaticals, and hybrid working policies are here to support you through life’s most meaningful moments. Financial wellbeing matters too, which is why we offer an enhanced pension scheme, access to a discount store, and free financial coaching through Bippit. To help you grow with confidence, we offer a structured training and development programme tailored to your role and department, equipping you with the tools, knowledge, and support you need to thrive. Read Less
  • Associate Director, Medical Compliance  

    - Harlow
    The opportunityWe are seeking an experienced Associate Director, Medic... Read More
    The opportunityWe are seeking an experienced Associate Director, Medical Compliance to provide strategic leadership within our UK & Ireland Medical Affairs organisation. You will bring your extensive medical compliance experience and expertise to this senior-level position, operating autonomously while delivering medical compliance excellence across all Teva activities in the UK and Ireland. We are looking for a candidate with a proven track record of compliance leadership and autonomous decision making in complex regulatory environments with minimal supervision and strategic mindset to proactively balance operational excellence with forward-thinking compliance initiatives. As a Subject Matter Expert (SME), you will drive medical compliance excellence, support key strategic initiatives, and make a meaningful impact on patient outcomes through compliant project implementation. Success in this role will be by measured by following metrics: Ensure full compliance with Teva SOPs, ABPI Code of Practice and IPHA code Zero PMCPA/HPRA complaints or successful defence of any complaints received Effective risk stratification of complex projects to ensure efficient implementation while maintaining compliance Achievement of business objectives through strategic thinking, proactively facilitating stakeholder dialogue and compliant operational processes Zero or minor observations in internal audits Stakeholder confidence metrics measured through internal surveys showing compliance function is seen as enabling (not blocking) business objectives A day in the life of an Associate Director, Medical Compliance... Final Signatory Activities Serve as final signatory for medical compliance approvals Review and approve materials, processes, and initiatives to ensure regulatory compliance Medical Compliance Leadership Actas primary PMCPA/MHRA and IPHA/ HPRA contact for medical compliance matters Develop and deliver ongoing training programs for final signatories (medical and commercial), AQPs, and reviewers Serve as main medical compliance liaison for TPE/Global teams Active participation as Compliance Committee member Facilitate Code training workshops across the organisation Liaise with Senior Manager, Meical Compliance and Therapy Area Leads to ensure PSP governance People Management Oversee activities and performance of Manager and Senior Manager, Medical Compliance Ensure Manager, Medical Compliance effectively maintains SOPs, compliance documentation (Glorya and Studium), and supports medical operations systems Drive efficient project implementation through proper system utilisation and approvals processes Ensure Senior Manager, Medical Compliance approves materials in a timely manner and provides governance to various projects. Audit and Inspection Leadership Lead and/ or support audits and inspections across multiple areas: Pharmacovigilance, Congresses, promotional materials, PSP, Veeva, and PMCPA/ IPHA Ensure audit readiness and compliance across all audited functions Strategic Support and Process Optimisation Provide SME support for process optimisation and continuous improvement initiatives Ensure Medical Affairs and Brand Plans comply with Teva SOPs, ABPI Code and IPHA code Ensure Medical Affairs KPls are aligned with regulatory requirements and company standards Support Medical Affairs Capability Mapping and Development programs Liaise with Compliance Officer on key projects System Administration Managing key platforms: Glorya (document management), Studium (training management), EngageMate (HCP engagement) and Veeva Promomats (promotional and non-promotional materials approval) Configure EngageMate and Veeva Promomats systems for compliant and efficient project implementation Strategic Project Support Partner with Senior Medical and Technical Director on high-priority initiatives Collaborate with project coordinators to implement key strategic projects Provide compliance expertise for ad hoc business requirements Your experience and qualifications Do you have...? Extensive experience as a final signatory with demonstrated independent decision-making authority Experience successfully leading and transforming a medical compliance function (not just participating) Proven track record of establishing compliance frameworks from scratch or significantly improving underperforming functions Demonstrated ability to challenge and influence key stakeholders on compliance matters without compromising standards Proven track record of SME input for process improvement Experience of managing and configuring platforms such as Veeva Promomats (promotional and non-promotional materials approval) Experience managing direct relationships with MHRA/PMCPA and HPRA/IPHA as the primary organisational representative Experience of PMCPA case defences where candidate was the lead strategist (not just a contributor) Demonstrated experience preventing PMCPA complaints through proactive stakeholder education and process improvements Evidence of preventing regulatory issues through proactive risk identification and stakeholder education Track record of participating in industry level initiatives to shape compliance frameworks Demonstrated experience making unpopular compliance decisions that were later validated Demonstrated experience of balancing compliance considerations and business goals using risk stratification strategies Proven ability to recover from compliance failures and implement sustainable improvements Evidence of successfully managing compliance during organisational change Are you...?  A qualified Physician or a Pharmacist with experience in the Pharmaceutical Industry. Desirable: Master's degree in business administration (MBA), Operations Management, or Process Improvement. Having a process improvement certification (Lean Six Sigma Green Belt/Black Belt, Lean Management, Change Management) will also be desirable. The final decision-maker (not advisor) on compliance matters Able to building or rebuilding stakeholder confidence after compliance failures Able to demonstrate openness to feedback and continuous learning mindset Willing to adapt approaches based on evidence and stakeholder feedback Able to exhibit collaborative leadership style with ability to influence Able to think outside the box while maintaining regulatory compliance Proactive Good communicator Enjoy a more rewarding choice We support our people through every stage of their journey with us. Our flexible reward platform puts you in control, empowering you to tailor your benefits to fit your lifestyle, priorities, and what matters most to you. With 25 days of annual leave that grows with your service, the flexibility to purchase additional days, and two dedicated volunteering days each year, your time off is truly yours to enjoy, recharge, and give back. We prioritise your health with private medical insurance, life assurance, critical illness cover, and income protection. Whether you're growing your family or pursuing new adventures, our enhanced maternity and paternity leave, sabbaticals, and hybrid working policies are here to support you through life’s most meaningful moments. Financial wellbeing matters too, which is why we offer an enhanced pension scheme, access to a discount store, and free financial coaching through Bippit. To help you grow with confidence, we offer a structured training and development programme tailored to your role and department, equipping you with the tools, knowledge, and support you need to thrive. Read Less
  • The opportunityThe Associate Director, Global Strategic Insights – Pip... Read More
    The opportunityThe Associate Director, Global Strategic Insights – Pipeline & Business Development will be responsible for strategic insight generation, helping define the long-term strategic vision, and commercial strategy primarily for Teva’s early stage pipeline assets and Business Development Opportunities - translating scientific innovation into long-term brand and business value.  We are seeking a strategist, who will serve as a key partner to the early-stage global product teams, R&D and Business Development teams - integrating market research and data, forecasting, competitive intelligence, and analytics to shape early pipeline decisions, and drive long-term growth in a complex and evolving therapeutic landscape.  This position can be based in the US (Parsippany), the Netherlands (Haarlem) or the UK. (In the UK, it can be based remotely.)  TRAVEL REQUIREMENTS Approximately up to 20% travel to support key meetings and cross-functional planning. How you’ll spend your day Pipeline Strategy: Lead insight generation to support early asset development, Target Product Profiles (TPPs), and go/no-go decisions.  Opportunity Assessment: Conduct market landscaping, unmet need analyses, and benchmarking to guide pipeline prioritization.  Business Development Support: Provide strategic and commercial evaluations for licensing, acquisition, or partnership opportunities.  Forecasting & Scenario Planning: Develop early-stage models and forecasts to support valuations and governance decisions.  Competitive Intelligence: Track emerging trends, scientific advances, and competitive dynamics to inform Teva’s innovation strategy.  Cross-Functional Collaboration: Partner across R&D, BD, and commercial teams to align insights and strategy globally.  Your experience and qualifications Bachelor’s degree required; advanced degree (MBA, MS, PhD, MPH) preferred.  A minimum of 7 years in strategic insights, pipeline strategy, business development, or commercial analytics within pharma/biotech.  Strong understanding of immunology and related therapeutic areas (autoimmune, inflammatory, biologics).  Proven ability to translate data into strategic recommendations that influence decision-making.  Experience supporting early-stage asset development and BD evaluations.  Excellent communication, stakeholder management, and presentation skills.  Read Less
  • The opportunityThe Director of Global Strategic Insights - Forecasting... Read More
    The opportunityThe Director of Global Strategic Insights - Forecasting will be responsible for leading our forecasting efforts across the Innovative pipeline with focus in CNS (Central Nervous System) and Immunology therapeutic areas. The ideal candidate will have extensive experience managing the forecast process for a diverse product portfolio, with a deep understanding of the US, EU, and other international markets. This role will be pivotal in driving forecast accuracy, improving processes, and providing strategic insights to support business decisions.  This position can be based in the US (Parsippany), the Netherlands (Haarlem) or the UK. (In the UK, it can be based remotely.)  TRAVEL REQUIREMENTS Approximately up to 20% travel to support key meetings and cross-functional planning.  How you’ll spend your day Forecasting Leadership: Lead the end-to-end global forecasting process for CNS and Immunology assets, ensuring accuracy and strategic relevance.  Market Analysis: Deliver deep analyses of market trends, competition, and dynamics across U.S., EU, and international markets.  Portfolio Management: Oversee forecasting for a diverse pipeline portfolio, aligning with global commercial objectives.  Process Improvement: Drive continuous improvement in forecasting methodologies, tools, and data integration.  Collaboration: Partner with regional, finance, R&D, and commercial teams to validate assumptions and ensure alignment across markets.  Insights & Reporting: Present clear, data-driven insights and forecasts to senior leadership, highlighting key trends, risks, and opportunities.  Your experience and qualifications Bachelor’s degree required in Business, Economics, Statistics, or related field; MBA or advanced degree preferred.  A minimum of 10 years of forecasting experience in pharma/biotech, ideally with CNS and Immunology exposure.  Deep understanding of U.S., EU, and global markets.  Strong analytical and quantitative skills, with proficiency in forecasting software and modelling tools.  Proven ability to communicate complex data clearly to senior stakeholders.  Experience leading process improvements and implementing forecasting best practices.  Excellent collaboration skills and ability to influence across global matrix environments.  Read Less
  • Maintenance Engineer  

    - Runcorn
    Who we areWe touch the lives of over 200 million patients every day, a... Read More
    Who we areWe touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point. Yet until today, you may not have heard of us. We’re Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world and we currently have a fantastic opportunity for a Maintenance Engineer to join our team on a Full Time, Permanent basis in Runcorn. At Teva Runcorn, we develop, manufacture and market innovative and affordable medicines, specialising in sterile liquid products mainly used for treating respiratory conditions using Blow-Fill-Seal technology as well as injectable Combination Products such as our MS treatment Copaxone.The Opportunity An Maintenance Engineer will be responsible for overseeing and coordinating maintenance activities for manufacturing equipment with a hands on approach. To strengthen the efficiency of the manufacturing systems to achieve maximum equipment performance whilst ensuring ongoing compliance with Health & Safety, cGMP/regulatory and corporate standards. To own equipment, procedures, maintenance plans and drive continuous improvements initiatives in order to implement industry best practice. Key Responsibilities: Execute planned and unplanned preventative maintenance tasks independently, to align with site KPI and schedule compliance Review and update maintenance schedules based on predicate knowledge to support ongoing business operations Drive forward plans for preventative and predictive maintenance to further reduce risk to equipment and processes Support production and other departments to minimise unplanned downtime and ensure effective communication Monitor equipment performance, propose and implement improvement activities to ensure optimum performance to improve equipment reliability Effective communication and influencing of key stakeholders Own and review Standard Operating Procedures and maintain training compliance Increase cost effectiveness through energy and maintenance saving initiatives Monitor expenditure when purchasing considering costs are with a reasonable range and within the maintenance budget Ensure right first time completion of all batch, operational and supporting documentation Support non-conformances, investigations, corrective actions and action root cause analysis effectively Minimising the impact of engineering activities on site operational targets through careful planning, communication and teamwork Ensure effective management of contractors on site to ensure safe, smooth and successful execution of activities Manage and implement small projects and drive improvements Working Hours 7 shifts over the course of a 2 week period including weekends Mixture of 6am-6pm or 6pm-6am shifts Your Experience And Qualifications Do you have? HND or Degree/post graduate qualification would be beneficial but not essential Significant relevant career experience and technical know how, is essential Related equipment experience operating in a pharmaceutical, or similar highly regulated environment A mechanical engineering background is required. Multi-skilled across both electrical and mechanical would be ideal Experience of equipment performance improvement, ideally within a GMP setting Are you? A strong communicator and proficient written skills Can demonstrate excellent proactive and reactive problem solving skills Very much 'hands on' with a keen eye for detail and high quality standards to your work Self-motivated with the ability to operate autonomously or within teams If so – we would value hearing from youWhat We Can Offer 23.5 paid annual shifts leave per year Private healthcare scheme through Bupa A formal training and development programme specific to your role and department Company pension – flexible employee and employer contributions Competitive salary and shift allowance at 40% of base salary Employee assistance programme A number of health benefits including: Life Assurance, Critical Illness Insurance, Income protection Plus many other flexible benefits via salary sacrifice: Cycle to work scheme, online and in store discounts and much more Read Less
  • The opportunityAs ‘Senior Director Head of Global Strategic Insights -... Read More
    The opportunityAs ‘Senior Director Head of Global Strategic Insights - Innovation Medicines’, you will lead a team responsible for strategic insight generation, helping define the long-term strategic vision, and commercial strategy for Teva’s neurology and immunology portfolio of medicines - translating scientific innovation into long-term brand and business value.  We are seeking an experienced pharmaceutical leader and strategist who is passionate and skilled at uncovering HCP, payer, patient and competitive insights to shape product strategies and investment decisions for our key innovative medicines from pipeline to inline assets, and BD opportunities. You will develop robust global forecasts and supporting assumptions across our portfolio for key governance stage gates, partnering closely with commercial regions, finance, R&D, and BD teams. This key leadership role will be a member of the Global Product Strategy (GPS) Leadership Team, and an active member of our capability transformation in the team. This position can be based in the US (Parsippany), the Netherlands (Haarlem) or the UK. (In the UK, it can be based remotely.)  TRAVEL REQUIREMENTS Approximately up to 20% travel to support key meetings and cross-functional planning. How you’ll spend your day Lead & Inspire: Build, mentor, and empower a high-performing global insights team; foster a culture of strategic thinking, curiosity, and innovation.  Generate Strategic Insights: Deliver actionable insights from HCP, patient, payer, and competitive data to guide brand, access, and investment strategies.  Forecasting & Business Strategy: Own and align global commercial forecasts with development plans and brand strategy; challenge and validate key assumptions.  Market Intelligence: Monitor competitors, market dynamics, and therapeutic trends to identify opportunities and inform decision-making.  Cross-Functional Leadership: Partner with Global Product, R&D, BD, Pricing & Access, and regional teams to drive strategic alignment across Teva’s portfolio.  Innovation & Best Practices: Introduce new methodologies, tools, and analytics approaches to enhance decision quality and competitive advantage.  Your experience and qualifications Bachelor’s degree in Life Sciences, Data Science, or related field; advanced degree (MBA, MSc, etc.) preferred.  A minimum of 15 years in pharma/biotech, including a minimum of 10 years in Insights, Analytics, or Strategy roles.  Deep experience in Neurology and/or Immunology; launch and pipeline experience essential.  Proven success influencing senior stakeholders in a global matrix environment.  Demonstrated leadership building and developing high-performing teams.  Experience working with Tier 1 markets (U.S. or EU5).  Strong analytical, strategic, and storytelling skills.  Read Less

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