Who we are Together we re on a mission to make good health more affordable and accessible to help millions around the world enjoy healthier lives It s a mission that bonds our people across nearly 60 countries and a rich diverse variety of nationalities and backgrounds Working here means working with the world s leading manufacturer of generic medicines and the proud producer of many of the products on the World Health Organization s Essential Medicines List Today at least 200 million people around the world take one of our medicines every single day An amazing number but we re always looking for new ways to continue making a difference and new people to make a difference with The opportunity The Scientific Writer is responsible for providing high-quality writing support and project management of scientific communication projects in compliance with good publication practices This includes abstracts congress presentations and manuscript for peer reviewed medical journals The role requires strong scientific knowledge excellent writing skills and the ability to translate complex clinical data into clear accessible content tailored to healthcare professionals HCPs patients and other stakeholders both external and internal How you ll spend your day Scientific Knowledge Possess the ability to understand a therapeutic area and product strategy to ensure scientific communication objectives are met Learns quickly to understand a new therapeutic area and the ability to adapt work across multiple therapeutic areas Translate complex scientific information and clinical trial data into content that meets the needs of various audiences including HCPs and patients Medical Writing and Publication Management An ability to write key scientific communication deliverables such as abstracts posters presentations and manuscripts Collaborate with Scientific Communication Leads and Therapeutic Area Leads to ensure global content is relevant up-to-date and aligned with evolving data Maintain robust version control and document tracking to ensure transparency audit-readiness and traceability in Teva s publication tracking tool Ability to adapt writing style for varied audiences such as specialist healthcare professionals patients nurses patients caregivers and other stakeholders Monitor scientific literature and new publications for impact on existing content and update accordingly Collaboration Review Ability to establish relationships with authors external experts and clinical trial investigators to ensure efficient development of high-quality publications Work cross-functionally with Medical Affairs Clinical Development Safety and other teams internally and externally to gain input and approval of scientific communication deliverables Support localization or adaptation of global content to meet regional or market-specific regulatory and cultural needs Quality Compliance Understand and apply knowledge of Good Publication Practices such as ICMJE Guidelines related to the development of scientific communication deliverables Follow internal SOPs style guides and established workflows to ensure consistency and compliance Conduct peer reviews of content developed by other writers to uphold high quality standards Innovation Continuous Improvement Participate in initiatives to enhance the content development process including use of AI tools structured content libraries and digital asset management systems Support the development of derivative content assets such as field medical affairs materials congress preparation content and other digital assets Your experience and qualifications Education Advanced degree PharmD PhD MD or Master s in Life Sciences or related field required Language English Professional level competency Experience 10-12 years of experience in medical writing medical information or scientific communications within the pharmaceutical biotech or medical device industry Experience with medical publication writing scientific literature analysis and congress content preparation Knowledge of Good Publication Practices and ICMJE Guidelines Familiarity with publication management systems e g Datavision Pubstrat Komodo and publication workflows Teva s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva s global policy that equal employment prospect be provided without regard to age race creed color religion sex disability pregnancy medical condition sexual orientation gender identity or expression ancestry veteran status national or ethnic origin or any other legally recognized status entitled to protection under applicable laws We are committed to a diverse and inclusive workplace for all If you are contacted for a job opportunity please advise us of any accommodations needed to support you throughout the recruitment and selection process All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience