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Consulting Project Team Lead - Investor
ClearView Healthcare Partners - London, United KingdomIndexed from Greenhouse Benefit evidence checked Jun 7, 2026posted 218 days agoWhy we showed this
Role: semantic matchUnspecified Finance From the posting source - Senior From the posting source Salary not disclosed Inferred from posting 401(k) reportedConsulting Project Team Lead - Investor London, United Kingdom Company Overview ClearView Healthcare Partners is a premier life sciences strategy consulting firm headquartered in Boston, with offices in San Francisco, New York City, London, Zurich and Gurgaon. Serving clients in the biopharmaceutical, medical device, and diagnostic spaces, we provide world-class strategic decision-making support across a diverse range of business issues. Our goal is to inform actionable recommendations that allow companies to achieve their business objectives. *We are not accepting any agency submissions for this position at this time The Investor pillar is dedicated to creating best practices and frameworks for buy-side and sell-side due diligence teams while advancing the firm's expertise in valuation strategies and deal-making within the healthcare sector. The team has extensive experience conducting diligences with our clients to maximize research value and provide strategic insights. Role Overview - Manages anywhere from 2 to upwards of 3 projects of varying complexity at a time depending on experience in the role. - Lead a broad range of typical ClearView Investor project types and should be able to support any situation and help instill order and structure to a project situation even if unfamiliar project type or content area. - Exhibits exceptional project management skills including raising issues to leadership early, designing impactful internal and external agendas and avoiding 'fire drills' with teams. - Elevates quality, clarity and simplicity of team output with early and clear direction, hypothesis-based thinking, simplification of storylines, impact of visuals and pithiness of writing. -
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Associate Director, Discovery Biology – Protein Homeostasis TRC
Bristol Myers Squibb - San Diego - CA - USIndexed from Workday Benefit evidence checked Jun 7, 2026posted 103 days agoWhy we showed this
Employer: "bristol"Employer: "myers"+1
Unspecified Other - Staff Plus From the posting source Salary not disclosed Equity Inferred from posting 401(k) reportedAssociate Director, Discovery Biology – Protein Homeostasis TRC San Diego - CA - US posted: Posted 30+ Days Ago
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Institutional & Specialty Sales Consultant - Stroke/Thrombosis - Burlington, VT
Bayer - Burlington,Vermont,United States | Residence Based,Vermont,United StatesIndexed from Eightfold Benefit evidence checked Jun 7, 2026posted 71 days agoWhy we showed this
Role: semantic matchUnspecified Data From the posting source - Mid From the posting source Salary not disclosed Inferred from posting 401(k) reportedInstitutional & Specialty Sales Consultant - Stroke/Thrombosis - Burlington, VT Burlington,Vermont,United States | Residence Based,Vermont,United States
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Pharmacovigilance Specialist- Consumer Engagement
Nestle - Country PhilippinesIndexed from Successfactorsposted 71 days agoWhy we showed this
Role: semantic matchUnspecified Healthcare From the posting source - Mid From the posting source Inferred from posting 4 wk leave Inferred from posting 4 wk non-birth leave Salary not disclosedPharmacovigilance Specialist- Consumer Engagement Country Philippines Position Summary As a Specialist, Pharmacovigilance , you will play a critical role in ensuring the safety and compliance of Nestle's VMS, Cosmetic, and OTC products You will manage adverse event case reviews, documentation, assessments, and MedWatch submissions in line with FDA regulatory guidelines. This position also supports Medical Nutrition products, collaborates with Medical Affairs, and contributes to product lifecycle improvements through scientific analysis and hypothesis generation. You will work closely with cross-functional teams including Regulatory & Scientific Affairs, Medical Affairs, Quality, and Consumer Engagement Services, reporting directly to the Pharmacovigilance Manage Key Responsibilities Review and assess adverse events daily for NHSc VMS brands in compliance with DSCPA. Conduct follow-up intakes with consumers and healthcare entities via phone, mail, or electronic channels, ensuring accurate documentation. Complete serious adverse event narratives using MedWatch Form 3500A and report to FDA within 15 days. Code adverse events by System Organ Classification in Salesforce for trend analysis. Initiate product reviews or investigations based on hypotheses or events of concern. Maintain up-to-date knowledge of FDA guidelines, regulatory requirements, and internal procedures. Stay informed on nutrients, ingredients, and structure-function claims. Perform other duties as assigned. Key Relationships NHSc US Regulatory Operations & Compliance team Regulator
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Hungarian
Bristol Myers Squibb - Location not specifiedIndexed from Custom Benefit evidence checked Jun 7, 2026posted 79 days agoWhy we showed this
Employer: "bristol"Employer: "myers"+3
Unspecified Other - Mid From the posting source Salary not disclosed Equity Inferred from posting 401(k) reportedHungarian Country | Hungary - BMS Careers Kiemelt lehetőségek Magyarországon > Sokszínűség és befogadás > Munkatársaink fejlődésének támogatása > Miért különleges a […]" /> Skip to content Career Areas Career Stories Join Talent Community BMS.com BMS.com Candidate Login HUN Careers Global Core Languages English Americas Argentina Spanish Brazil Portuguese Canada English / French Chile Spanish Colombia Spanish Peru Spanish United States English Mexico Spanish Asia Pacific Australia English China Simplified Chinese India English Japan Japanese Korea Korean Taiwan Traditional Chinese Europe Austria German Belgium English / Dutch / French Czechia English Denmark Danish Finland Finnish France French Germany German / English Greece Greek Hungary Hungarian Ireland English Italy Italian Luxembourg English Netherlands Dutch / English Norway Norwegian Poland Polish / English Portugal Portuguese Romania Romanian Spain Spanish Sweden Swedish Switzerland German / French / English United Kingdom English Middle East Israel English Turkey Turkish Careers Home Life at BMS Life at BMS Inclusion & Diversity Developing Our People Awards & Recognitions Our Benefits QUICK LINKS Global Patient Week Our Stories Sustainability Commitments Career Areas Career Areas Research & Development Global Product Development & Supply Commercial & Access Corporate Contract Positions Military and Veterans RayzeBio QUICK LINKS Advanced Degree Programs Areas of Focus In the Pipeline Our Medicines Student Opportunities Student Opportunities Internships & Co-ops Leadership Development Programs Advanced Degree Programs QUICK LINKS BMS on Handshake Events How We Recruit Career Stories Search Jobs Search this site Join Talent Community BMS.com Candidate Login HUN Careers Global Core Languages English Americas Argentina
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Principal Scientist - Cell Therapy Translational Research
Bristol Myers Squibb - Seattle 400 Dexter - WA - USIndexed from Workday Benefit evidence checked Jun 7, 2026posted 93 days agoWhy we showed this
Employer: "bristol"Employer: "squibb"+1
Unspecified Data From the posting source - Staff Plus From the posting source Salary not disclosed Equity Inferred from posting 401(k) reportedPrincipal Scientist - Cell Therapy Translational Research Seattle 400 Dexter - WA - US posted: Posted 21 Days Ago
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Account Manager, Coronary Therapies (South Wales, Bristol & surrounding areas)
Boston Scientific - Additional Posting Location(s) United Kingdom-Cardiff|United Kingdom-Bristol|United Kingdom-Swindon|United Kingdom-Swansea|United Kingdom-Oxford|United Kingdom-GloucesterIndexed from Successfactors Benefit evidence checked May 7, 2026posted 71 days agoWhy we showed this
Title: "bristol"Role: semantic matchUnspecified Sales From the posting source - Senior From the posting source Resolvable source Verified parental leave: 8 wksource Resolvable source Verified non-birth-parent leave: 8 wksource Salary not disclosed Equity Inferred from posting 401(k) reportedAccount Manager, Coronary Therapies (South Wales, Bristol & surrounding areas) Additional Posting Location(s) United Kingdom-Cardiff|United Kingdom-Bristol|United Kingdom-Swindon|United Kingdom-Swansea|United Kingdom-Oxford|United Kingdom-Gloucester Additional Locations: Additional Posting Location(s) United Kingdom-Cardiff|United Kingdom-Bristol|United Kingdom-Swindon|United Kingdom-Swansea|United Kingdom-Oxford|United Kingdom-Gloucester Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions. About the role As an Account Manager (AM), you will take responsibility for managing the full end-to-end sales process for assigned customer segments. You will identify and capitalise on commercial opportunities in the region, develop account plans across your customer base, and drive the execution of both regional and local sales strategies. The primary purpose of this role is to accelerate business growth, expand BSC's market share, and secure strong product positioning, engaging both clinical and economic stakeholders through targeted commercial activity. This is a permanent role within the UK South team, representing the Coronary Therapies portfolio. The territory is expected to broadly cover areas such as the Bristol region, Gloucestershire, Wiltshire, Oxfordshire and South Wales. You will sit within the Inte
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Simplified Chinese
Bristol Myers Squibb - Location not specifiedIndexed from Custom Benefit evidence checked Jun 7, 2026posted 79 days agoWhy we showed this
Employer: "bristol"Employer: "squibb"+3
Unspecified Other - Mid From the posting source Salary not disclosed Equity Inferred from posting 401(k) reportedSimplified Chinese Country | China - BMS Careers 职位机会 > 多元和包容 > 职业发展优势 > 中国大陆的办公地点 > 职场生活 > 企业成就 > 与我们共事 我们有明确的目标和包容的文化,您有机会在擅长的领域从事 顶尖的工作,这些是让您在职业抉择中选择百时美施贵宝的重 要理由。查看我们的最新奖项和荣誉,深入了解我们如何确保员工在职场内外都能取得成功。 职位机会 商业和准入 医学事务 研发 查看所有职位(中国) 查看所有职位(全球) 多元和包容 我们的员工来自全球,致力于打造敏捷、具有创新精神且有责任 感的高绩效文化。 职业发展优势 我们致力于营造能充分发挥每一位员工潜力的工作环境,鼓励员工追求创新想法,强化职业技能并获得宝贵经验,从而打造个人职业生涯。我们始终致力于培养员工,不断追求卓越,开拓进取, 这对于我们自身发展以及保持在生物制 药领域的领导地位至关重要。 数字化学习 无论何时,您都可以获取海量的在线资料,学习并掌握所需要的专业技能。通过LinkedIn Learning提供的各种专业学习和发展资源,您可以在我们庞大的资源库中获得多方面专业性内容,并附有多种语言版本。 发展课程 领导力与管理课程:员工是公司宝贵的财富和资源,我们十分重视对员工的培养和发展。公司鼓励员工努力学习专业知识, 不断提升,同时也为员工提供多维度的线下课程(比如BMS全球通用的领导力课程以及中国区领导力发展课程)和一些定制化的人才培养项目(比如ELP ,RISING ,MCP等)以提升其所需的知识、技能和能力,从而提高绩效和管理技能,实现员工和公司的共同成长。 培养管理者能力: 我们通过向新任或经验丰富的管理者和高级领导者提供虚拟学习和课堂学习,致力于推动管理者和高级领导的成长。 工作经验 我们认为,员工通过实践经历能够获得更多经验。依靠团队和同事间的互相帮助,有助于帮助你面对工作中的挑战,同时最大程度获得提升与进步。 团队协作 我们的工作极具挑战性,您不会独自面对一切难题。您会与经验更丰富的同事展开团队协作,通过向其征询建议,会帮助您不断前进。 除了日常的指导和支持,多元化和包容性组织的成员可与全球范围内的员工一同接受导师制的培养发展。 中国大陆的办公地点 上海市闵行工厂 上海市会德丰国际广场 查看所有职位 职场生活 患者信任我们,我们信任您。我们提供完善的薪酬福利体系,可充实员工需求,为员工增权赋能,并使他们爱岗敬业。 […]" /> Skip to content Career Areas Career Stories Join Talent Community BMS.com BMS.com Candidate Login CHN Careers Global Core Languages English Americas Argentina Spanish Brazil Portuguese Canada English / French Chile Spanish Colombia Spanish Peru Spanish United States English Mexico Spanish Asia Pacific Australia English China Simplified Chinese India English Japan Japanese Korea Korean Taiwan Traditional Chinese Europe Austria German Belgium English / Dutch / French Czechia English Denmark Danish Finland Finnish France French Germany German / English Greece Greek Hungary Hungarian Ireland English Italy Italian Luxembourg English Netherlands Dutch / English Norway Norwegian Poland Polish / English Portugal Portuguese Romania Romanian Spain Spanish Sweden Swedish Switzerland German / French / English United Kingdom English Middle East Israel English Turkey Turkish Careers Home Life at BMS Life at BMS Inclusion & Diversity Developing Our People Awards & Recognitions Our Benefits QUICK LINKS Global Patient Week Our Stories Sustainability Commitments Career Areas Career Areas Research & Development Global Product Development & Supply Commercial & Access Corporate Contract Positions Military and Veterans RayzeBio QUICK LINKS Advanced Degree Programs Areas of Focus In the Pipeline Our Medicines Student Opportunities Student Opportunities Internships & Co-ops
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Japanese
Bristol Myers Squibb - Location not specifiedIndexed from Custom Benefit evidence checked Jun 7, 2026posted 79 days agoWhy we showed this
Employer: "squibb"Employer: "myers"+3
Unspecified Other - Mid From the posting source Salary not disclosed Equity Inferred from posting 401(k) reportedJapanese Country | Japan - BMS Careers キャリア採用 > 新卒採用 ダイバーシティ&インクルージョン > ダイバーシティ&インクルージョン活動への取り組み > ダイバーシティ活動へのサポート > スポンサーシップ活動 > I私たちのバリュー > 人材育成 > 社員を支援する制度 > キャリア開発制度> 採用情報 ブリストル マイヤーズ スクイブには、深刻な病気を抱える患者さんを助けるという使命の下、業界の最前線で活躍するチームの一員となり、プロとして学び成長する環境が整っています。素晴らしい仲間と共に素晴らしい仕事をするという経験は、どこでも得られるものではありません。 もっと詳しく知る キャリア採用 現在募集中の中途採用へのご応募はこちらよりお進みください。 本社または、愛知工場を希望される方 > 臨床開発部門でのキャリアにご興味の方は、こちらより職種紹介をぜひご確認ください。 障がい者採用 現在募集中の障がい者採用へのご応募はこちらよりお進みください 本社または、愛知工場を希望される方 新卒採用 2028年4月入社の方 Internship(文理不問)への応募はこちら ダイバーシティ&インクルージョン ブリストル マイヤーズ スクイブは、人材こそが最大の財産であると考えます。性別や国籍、年齢だけでなく、個々の価値観や考え方、性格の多様性を受け入れ、一人ひとりの人材を活かす「ダイバーシティ」はもちろん、一人ひとりが自分らしく組織に参加・貢献できる機会を提供し、イノベーションや相互成長を促す「インクルージョン」の推進にも取り組んでいます。 より良く、より柔軟に、より多様性ある企業へ 性差による障壁を取り除く: 出産や育児などのライフイベントを乗り越え、性別に関わりなく活躍できる環境を整えています。 年齢による障壁を取り除く: 若年層従業員の早期育成や、シニア従業員の活躍の場を広げる施策、シニアの知見・能力を活用するための定年後再雇用プログラムを推進しています。 […]" /> Skip to content Career Areas Career Stories Join Talent Community BMS.com BMS.com Candidate Login JPN Careers Global Core Languages English Americas Argentina Spanish Brazil Portuguese Canada English / French Chile Spanish Colombia Spanish Peru Spanish United States English Mexico Spanish Asia Pacific Australia English China Simplified Chinese India English Japan Japanese Korea Korean Taiwan Traditional Chinese Europe Austria German Belgium English / Dutch / French Czechia English Denmark Danish Finland Finnish France French Germany German / English Greece Greek Hungary Hungarian Ireland English Italy Italian Luxembourg English Netherlands Dutch / English Norway Norwegian Poland Polish / English Portugal Portuguese Romania Romanian Spain Spanish Sweden Swedish Switzerland German / French / English United Kingdom English Middle East Israel English Turkey Turkish Careers Home Life at BMS Life at BMS Inclusion & Diversity Developing Our People Awards & Recognitions Our Benefits QUICK LINKS Global Patient Week Our Stories Sustainability Commitments Career Areas Career Areas Research & Development Global Product Development & Supply Commercial & Access Corporate Contract Positions Military and Veterans RayzeBio QUICK LINKS Advanced Degree Programs Areas of Focus In the Pipeline Our Medicines Student Opportunities Student Opportunities Internships & Co-ops Leadership Development Programs Advanced Degree Programs QUICK LINKS
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Consulting Project Team Lead - Pricing & Market Access
ClearView Healthcare Partners - London, London, United KingdomIndexed from Greenhouse Benefit evidence checked Jun 7, 2026posted 218 days agoWhy we showed this
Role: semantic matchUnspecified Other - Senior From the posting source Salary not disclosed Inferred from posting 401(k) reportedConsulting Project Team Lead - Pricing & Market Access London, London, United Kingdom Company Overview ClearView Healthcare Partners is a premier life sciences strategy consulting firm headquartered in Boston, with offices in San Francisco, New York City, London, Zurich and Gurgaon. Serving clients in the biopharmaceutical, medical device, and diagnostic spaces, we provide world-class strategic decision-making support across a diverse range of business issues. Our goal is to inform actionable recommendations that allow companies to achieve their business objectives. *We are not accepting any agency submissions for this position at this time Our Pricing and Market Access (P&MA) practice integrates strategic consulting with deep industry knowledge to optimize both launch and long-term pricing strategies. The P&MA practice supports pharmaceutical, biotech, and medtech clients by bridging product goals with market-specific evidence requirements, payer expectations, and competitive threats, ensuring successful commercialization globally. Role Overview - Manages anywhere from 2 to upwards of 5 projects of varying complexity at a time depending on experience in the role. - Lead a broad range of typical ClearView P&MA project types and should be able to support any situation and help instill order and structure to a project situation even if unfamiliar project type or content area. - Exhibits exceptional project management skills including raising issues to leadership early, designing impactful internal and external agendas and avoiding 'fire drills' with teams. - Elevates quality, clarity and simplicity of team output with early and clear direction, hypothesis-based thinking, simplification of storylines, impact of visuals and pithiness of
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Account Manager, Coronary Therapies (South Wales, Bristol & surrounding areas)
Boston Scientific Corporation - Swindon, United Kingdom | United Kingdom-Gloucester, United Kingdom-Swansea, United Kingdom-Oxford, United Kingdom-Cardiff, United Kingdom-Swindon, United Kingdom-BristolIndexed from Eightfold Benefit evidence checked Jun 7, 2026posted 71 days agoWhy we showed this
Title: "bristol"Role: semantic matchUnspecified Sales From the posting source - Senior From the posting source Salary not disclosed Equity Inferred from posting 401(k) reportedAccount Manager, Coronary Therapies (South Wales, Bristol & surrounding areas) Swindon, United Kingdom | United Kingdom-Gloucester, United Kingdom-Swansea, United Kingdom-Oxford, United Kingdom-Cardiff, United Kingdom-Swindon, United Kingdom-Bristol
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Quality Assurance Manager - Medical Devices
AbbVie Inc. - Sligo, SO, IrelandIndexed from Smartrecruiters Benefit evidence checked May 7, 2026posted 74 days agoWhy we showed this
Role: semantic matchUnspecified Healthcare From the posting source - Senior From the posting source Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Equity Inferred from posting 401(k) reportedQuality Assurance Manager - Medical Devices Sligo, SO, Ireland Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: AbbVie invites you to join our cutting-edge pharmaceutical facility in Sligo, nestled in a region known for its vibrant community and scenic beauty. Embrace an opportunity to grow your career while contributing to meaningful innovations that enhance global health. An exciting role has opened up on our Ballytivnan site in Sligo. We are currently looking for a Quality Manager overseeing the Medical Device Quality team, reporting to the Quality Site Head. You will oversee the whole quality function for the medical device business on site. You'll ensure compliance with quality standards and regulatory requirements, leading a dedicated team of quality professionals. Responsibilities Quality Assurance & Control: Oversee testing of raw materials, manufacturing quality control, and product validation. Team Leadership: Manage and lead a team responsible for compliance and quality oversight. Regulatory Compliance: Ensure adherence to corporate and regulatory requirements. Performance Reporting: Report on the performance of the quality management system to senior management. Issue
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Institutional & Specialty Sales Consultant - Stroke/Thrombosis | Flushing, NY
Bayer - Queens,New York,United States | Residence Based,New York,United StatesIndexed from Eightfold Benefit evidence checked Jun 7, 2026posted 71 days agoWhy we showed this
Role: semantic matchUnspecified Data From the posting source - Mid From the posting source Salary not disclosed Inferred from posting 401(k) reportedInstitutional & Specialty Sales Consultant - Stroke/Thrombosis | Flushing, NY Queens,New York,United States | Residence Based,New York,United States
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Consulting Project Team Lead - Investor (Multiple offices)
ClearView Healthcare Partners - New York, New York, United States, Boston, Massachusetts, United States, San Francisco, California, United StatesIndexed from Greenhouse Benefit evidence checked Jun 7, 2026 Comp disclosed in postingposted 218 days agoWhy we showed this
Role: semantic matchUnspecified Finance From the posting source - Senior From the posting source Salary not disclosed From the posting source Inferred from posting 401(k) reportedConsulting Project Team Lead - Investor (Multiple offices) New York, New York, United States, Boston, Massachusetts, United States, San Francisco, California, United States Company Overview ClearView Healthcare Partners is a premier life sciences strategy consulting firm headquartered in Boston, with offices in San Francisco, New York City, London, Zurich and Gurgaon. Serving clients in the biopharmaceutical, medical device, and diagnostic spaces, we provide world-class strategic decision-making support across a diverse range of business issues. Our goal is to inform actionable recommendations that allow companies to achieve their business objectives. *We are not accepting any agency submissions for this position at this time The Investor pillar is dedicated to creating best practices and frameworks for buy-side and sell-side due diligence teams while advancing the firm's expertise in valuation strategies and deal-making within the healthcare sector. The team has extensive experience conducting diligences with our clients to maximize research value and provide strategic insights. Role Overview - Manages anywhere from 2 to upwards of 3 projects of varying complexity at a time depending on experience in the role. - Lead a broad range of typical ClearView Investor project types and should be able to support any situation and help instill order and structure to a project situation even if unfamiliar project type or content area. - Exhibits exceptional project management skills including raising issues to leadership early, designing impactful internal and external agendas and avoiding 'fire drills' with teams. - Elevates quality, clarity and simplicity of team output with early and clear
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Pharmacovigilance Scientist
Tonix Pharmaceuticals Holding Corp - Berkeley Heights, NJIndexed from Greenhouse Benefit evidence checked Jun 13, 2026 Comp disclosed in postingposted 142 days agoWhy we showed this
Role: semantic matchUnspecified Healthcare From the posting source - Mid From the posting source $124K-$170K From the posting source Equity Inferred from posting 401(k) reportedPharmacovigilance Scientist Berkeley Heights, NJ Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8 mg) is the first new treatment for fibromyalgia in adults in more than 15 years. Tonix's CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® Symtouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is investigating TONMYA® in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti- Borrelia OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. In addition, the Company is progressing TNX-2900 (intranasal potentiated oxytocin), which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. To learn more, visit www.tonixpharma.com and follow the Company on LinkedIn and X . *Tonix's product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication. Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property of their respective owners. Position Overview Tonix is seeking an experienced Pharmacovigilance Scientist
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Senior Analyst - Store Brand
Perrigo - LondonIndexed from Successfactors Benefit evidence checked Jun 7, 2026posted 71 days agoWhy we showed this
Role: semantic matchUnspecified Marketing From the posting source - Senior From the posting source Salary not disclosed Equity Inferred from posting 401(k) reportedSenior Analyst - Store Brand London At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All . We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone , we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo . We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging. Join us on our One Perrigo journey as we evolve to win in self-care. Description Overview Perrigo, a leading global healthcare provider, is recruiting for a Storebrand Manager in the North Europe Cluster, based in London. The role focuses on shaping and strengthening Perrigo's UK Storebrand portfolio across key OTC categories including Pain, Sleep, Upper Respiratory, Gastro, and Nicotine Replacement Therapy (NRT). This role plays a critical part in defining the future UK Storebrand portfolio. Using customer, market, and internal data, the Storebrand Manager will identify and evaluate growth opportunities and progress initiatives through the Stage‑Gate process in close collaboration with Commercial, Value Chain, and Global teams. The role also ensures strong execution of approved initiatives and reports direct
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Senior Director, Commercial, UK
Revolution Medicines - Remote (UK)Indexed from Greenhouse Benefit evidence checked Jun 7, 2026posted 116 days agoWhy we showed this
Role: semantic matchRemote From the posting source Sales From the posting source - Director Plus From the posting source Salary not disclosed Equity Inferred from posting 401(k) reportedSenior Director, Commercial, UK Remote (UK) Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: The Senior Director, Commercial, UK is responsible for defining and executing the local commercial strategy for oncology products. This role is accountable for building the commercial organization, driving launch and growth performance, and ensuring strong alignment across Medical Affairs, Market Access, and other key functions. The incumbent needs to proactively recognize and address relevant systemic (e.g. health care structures, competitors, data gaps, diagnostic challenges, missing advocacy) and HCP related opportunities (e.g. therapeutic gaps, differentiation, economical attributes, clear messaging of patient- and physician relevant benefits). The Senior Director Commercial will further oversee the generation of insights from the therapeutic field, and translate these insights into a comprehensive, cross-functional strategy. Supporting a clear positioning and aligned communication approach, the incumbent will in addition secure the development and implementation of tactics and tools for the field force to effectively address customer needs. Responsibilities: - Act as the Commercial Lead
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Junior Consultant - Pharma
IQVIA - Kampenhout, BelgiumIndexed from Workday Benefit evidence checked Jun 13, 2026posted 75 days agoWhy we showed this
Role: semantic matchUnspecified Data From the posting source - Entry From the posting source Salary not disclosed Equity Inferred from posting 401(k) reportedJunior Consultant - Pharma Kampenhout, Belgium posted: Posted 3 Days Ago
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Institutional & Specialty Sales Consultant - Stroke/Thrombosis - Richmond, VA
Bayer - Richmond,Virginia,United StatesIndexed from Eightfold Benefit evidence checked Jun 7, 2026posted 71 days agoWhy we showed this
Role: semantic matchUnspecified Data From the posting source - Mid From the posting source Salary not disclosed Inferred from posting 401(k) reportedInstitutional & Specialty Sales Consultant - Stroke/Thrombosis - Richmond, VA Richmond,Virginia,United States
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Executive Director, Global Patient Safety Quality and Compliance - Pharmacovigilance
Revolution Medicines - Redwood City, California, United StatesIndexed from Greenhouse Benefit evidence checked Jun 7, 2026 Comp disclosed in postingposted 134 days agoWhy we showed this
Role: semantic matchUnspecified Healthcare From the posting source - Director Plus From the posting source $265K-$331K From the posting source Equity Inferred from posting 401(k) reportedExecutive Director, Global Patient Safety Quality and Compliance - Pharmacovigilance Redwood City, California, United States Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: We are seeking a skilled and experienced Executive Director (ED) of Global Patient Safety (GPS) Quality and Compliance to join our dynamic team. The ED GPS Quality and Compliance is responsible for the strategy, development, oversight, and execution of the pharmacovigilance quality management system (PV-QMS) within the organization. This role ensures the safety of patients and the overall positive benefit-risk of RevMed pharmaceutical products by driving compliance with global pharmacovigilance regulations and fostering a culture of safety and vigilance. The responsibilities of this role include oversight of the PV-QMS , PV training strategy, PV controlled documentation, inspection and audit management, ensuring inspection readiness, Corrective Action Preventive Action (CAPA) management, Quality Assurance (QA), and maintenance of Good Clinical Practice (GCP), and Good Pharmacovigilance Practices (GVP) in partnership with GPS management, QA, and staff. The ED of GPS Quality
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Senior Manager, Commercial Regulatory Affairs
Revolution Medicines - Redwood City, California, United StatesIndexed from Greenhouse Benefit evidence checked Jun 7, 2026 Comp disclosed in postingposted 134 days agoWhy we showed this
Role: semantic matchUnspecified Operations From the posting source - Senior From the posting source $164K-$205K From the posting source Equity Inferred from posting 401(k) reportedSenior Manager, Commercial Regulatory Affairs Redwood City, California, United States Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: Revolution Medicines is seeking a Senior Manager, Commercial Regulatory Affairs to partner closely with the cross-functional teams to ensure that all promotional and medical communication strategies are compliant with applicable regulations, industry standards, and internal policies. This role will help enable successful product commercialization while upholding regulatory integrity and scientific accuracy. As part of the Regulatory Affairs function, the Senior Manager will work under supervision to provide strategic regulatory advice on advertising/promotion and medical materials to the US organization for assigned products in accordance with business goals and objectives, FDA regulations/guidances, pharma guidelines, and company policy. The position can be based at our Redwood City, CA site in a hybrid work schedule (preferred) or remote-based with quarterly and as needed travel. Required Skills, Experience and Education: - Serves as a primary or secondary regulatory advertising and promotion reviewer for assigned products on
- posted 74 days ago
Why we showed this
Title: "bristol"Role: semantic matchAssociate Financial Operations Analyst (Bristol) Bristol, UK Associate Financial Operations Analyst (Bristol) Bristol, UK Posted Wednesday, May 27, 2026 Associate Financial Operations Analyst (Central Bristol) More than a mission, C2FO is a better financial system changing the way every business gains access to the working capital they need to thrive. At C2FO, everyone is an employee-owner which means we're all invested in our work and team members. We're a company of team players and self-starters finding new and innovative ways to get things done. If you're excited to learn, grow, and leave your mark on our fast-growing organization, C2FO may be the place for you. About C2FO Headquartered in Kansas City, USA, C2FO has more than 400+ employees worldwide, with operations throughout North America, Europe, India, Asia Pacific, and Australia. C2FO is the world's largest on-demand working capital platform. Our mission is to ensure every business has the capital needed to thrive and we have delivered more than $500+ billion in funding to businesses since our founding. How do we do this? By providing fast, flexible, and equitable access to low-cost capital through our easy-to-use platform. We provide technology with a human touch, giving our customers the direct support they need and ensuring our team members have the tools, resources, and work environment they need to deliver on our promise to customers. With the C2FO platform, businesses worldwide have more working capital to fuel their growth, create jobs and develop new products. Benefits At C2FO, we take care of our
- posted 71 days ago
Why we showed this
Role: semantic matchTubing Inspector/Cutter Trenton, GA Expected Travel: Requisition ID: 13858 About Teleflex Incorporated As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare. Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ - trusted brands united by a common sense of purpose. At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com. OEM - Teleflex Medical OEM is a leading global provider of product development and production services for medical device manufacturers. We set ourselves apart with deep expertise, decades of experience, a dedication to design for manufacturability, and extensive, in-house capabilities, which include engineering, regulatory services, material selection and formulation, prototyping, manufacturing, assembly and packaging. We deliver industry-changing innovations and next-generation solutions for extrusions; diagnostic and interventional catheters; balloons and balloon catheters; sheath/dilator sets; specialty sutures, braids and fi
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Consulting Project Team Lead - Launch & Commercialization (Multiple offices)
ClearView Healthcare Partners - Boston, Massachusetts, United States, New York, New York, United States, San Francisco, California, United StatesIndexed from Greenhouse Benefit evidence checked Jun 7, 2026 Comp disclosed in postingposted 158 days agoWhy we showed this
Role: semantic matchUnspecified Other - Senior From the posting source Salary not disclosed From the posting source Inferred from posting 401(k) reportedConsulting Project Team Lead - Launch & Commercialization (Multiple offices) Boston, Massachusetts, United States, New York, New York, United States, San Francisco, California, United States Company Overview ClearView Healthcare Partners is a premier life sciences strategy consulting firm headquartered in Boston, with offices in San Francisco, New York City, London, Zurich and Gurgaon. Serving clients in the biopharmaceutical, medical device, and diagnostic spaces, we provide world-class strategic decision-making support across a diverse range of business issues. Our goal is to inform actionable recommendations that allow companies to achieve their business objectives. *We are not accepting any agency submissions for this position at this time Our Launch and Commercialization (L&C) Team brings specialized expertise and end-to-end support that turns innovative drugs from ideas into market success stories. Powered by our deep knowledge of market dynamics, clinical insights, and commercialization understanding, we craft tailored launch strategies and customer engagement strategies that deliver sustained results for clients. With proven results from launching over 100+ new molecular entities and indications, ClearView Launch and Commercialization is where impact meets innovation. Project Lead (PL) Role Overview Responsibilities - Manage between 2 to 5 projects at once and all corresponding responsibilities at any given time. - Lead a broad range of typical ClearView project types and should be able to support any situation and help instill order and structure to a project situation even if unfamiliar project type or content area. - Exhibit exceptional project management skills including raising issues to leadership early, designing impactful internal and
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