Developing commercialization strategies for novel targeted therapies in RAS-addicted cancers, with cross-functional team collaboration. 12+ years biotech/pharma experience in oncology marketing and European product launches required. Focus on novel targeted therapies for RAS-addicted cancers.
Leading strategy for clinical regulatory submissions for rare disease therapies. 8-10 years regulatory medical writing experience leading major US/EMA submissions required. Conference attendance opportunity.
FP&A for balance sheet and cash flow at global healthcare manufacturer with 110,000+ employees. Experience with SAC Planning or similar financial reporting tools preferred. Monthly sales reporting and dashboard creation for pharmaceutical operations.
Foundational content AI services and core platform indexing for AEM cloud services. Solid Java programming and experience with AI/ML systems required. Accessible recruiting process with disability accommodations.
Structural biology modeling and deep learning software development for de novo antibody design at global healthcare firm. Proficiency in Python and MLOps frameworks like Hydra or Weights & Biases required. Lab-in-the-loop research environment with public computational portfolio preferred.
Converting engineering data into manufacturing bills of material for business aircraft cabin completions. Proficiency in PDM/PLM systems and 3D CAD software required. Access to latest aviation manufacturing technologies and tools.
Product development projects within a multinational pharmaceutical and diagnostics environment. Current enrollment in a Bachelor's or Master's degree program required. Dedicated obstacle removal support and structured career pathing.
Financial oversight for branch offices and legal entities exporting medicines to 80+ countries. Proficiency in Microsoft Power Platform and Citizen Development project delivery required. Inclusive work environment with reasonable accommodation support.
Directing and producing cinematic brand films and global shoots for a pharmaceutical company with 76,000+ employees. Extensive portfolio in high-impact visual storytelling and narrative concept development required. Global travel for on-site production, inclusive workplace environment.
Design and execution of observational studies to inform clinical development and regulatory strategy at global pharmaceutical manufacturer. 2-4 years of healthcare or real-world data research experience required. Cross-functional collaboration across development and pharma teams, statistical software application.
Financial oversight of pharmaceutical export transactions and contract reviews for global distribution markets. Proficiency in Microsoft Power Platform and accounting experience required. Reasonable accommodation for recruitment and disability provided.
Quality oversight for small-molecule drug trials and CRO collaboration at biotech with 1,200+ employees. Extensive GCP auditing and health authority interaction experience required. 40-hour week, 25-30 days vacation.
Global product launch strategy and advocacy leadership for pharmaceutical franchises across international markets. Proven success in large-scale, geographically dispersed team management required. Reasonable accommodation for recruitment and disability provided.
Hands-on laboratory testing and sample preparation for parenteral dosage forms at global CDMO. Degree in Pharmaceutical Sciences and basic laboratory environment familiarity required. 40-hour week, inclusive workplace culture.
Global brand standards and design quality oversight for a network of pharmaceutical production and research facilities. University-level Master’s Degree in Architecture and strong conceptual design skills required. High-level stakeholder management across international sites, focus on corporate identity consistency.
Drug substance lifecycle management and technology transfers to global CDMO networks for biopharmaceutical manufacturing. Seasoned CMC leadership experience and PhD in Chemistry or related field preferred. Global matrix team collaboration, 30 days vacation, and flexible hybrid work model.
Global manufacturing roadmap design for small molecule, large molecule, and device technologies at healthcare firm with 100,000+ employees. 15+ years pharmaceutical or biotech leadership experience required. Cross-functional collaboration with technical development and engineering teams.
Regional reputation management and executive visibility for oncology pipeline at clinical-stage biotech. 10 years healthcare communications and multi-market leadership experience required. Cross-functional stakeholder management in 500+ employee organization.
Analytical method transfers to CDMO networks for commercial manufacturing of life-changing healthcare solutions. Advanced degree and 7+ years industry experience in analytical procedure lifecycles required. Global collaboration across manufacturing sites with 30 days vacation.
Consulting clients on IRT system setups and authoring user requirement documents for clinical research protocols. Mandatory IRT system design experience and SQL knowledge required. Global project scope with 5-person cross-functional team coordination.
Long-term revenue forecasting and patient journey mapping for new drug programs at pharmaceutical firm with 75,000+ employees. Minimum 10 years of biotech or pharmaceutical industry experience required. Advanced degree and multilingual skills preferred.
Long-term revenue forecasting and patient journey mapping for new drug programs at global pharmaceutical manufacturer. Minimum 10 years of biotech or pharma industry experience required. Advanced degree or MBA strongly preferred.
High-touch technical support for executives and GxP-regulated applications at oncology-focused biotech firm. Proficiency in Windows 11, Intune, and MDM troubleshooting required. Small team environment with systems lifecycle management focus.
Testing liquid and lyophilized drug product samples using pH, osmolality, and UV-Vis analytical methods. Basic laboratory skills and wet lab techniques required. High-performance compensation programs, agile career paths.
Go-to-market strategy and value proposition development for drug substance manufacturing platforms at global CDMO. Extensive strategic marketing experience in pharma or biotech sectors required. Global cross-functional team leadership, 30 days vacation.
Daily and weekly line maintenance checks including release to service for civil aviation fleets. Valid EASA Part-66 license with A320 and B737 or B757/B767 type ratings required. Global deployment opportunities, shift-based work in high-security hangar environments.
ETL pipeline design and MongoDB schema implementation for FAIR data curation at pharmaceutical firm with 10,000+ employees. Proficiency in Python scripting and ETL orchestration required. Partial home office, 30 days vacation.
Strategic planning and project oversight for the Head of Clinical Supply Services at a global pharmaceutical firm. Over 5 years of industry experience and a background in strategic consulting preferred. High-level stakeholder connectivity, cross-functional initiative management.
Global commercialization and lifecycle management for rare disease therapies at pharmaceutical firm with 75,000+ employees. 15 years of commercial leadership and proven product launch track record required. Flexible hybrid work, inclusive culture with reasonable accommodation support.
Global data privacy liaison and AI usage advisory for information governance at healthcare firm with 100,000+ employees. Minimum 5 years People & Culture experience and data security mastery required. Hybrid work model, 40-hour week.