Drug product manufacturing and validation SME for rare disease biopharmaceuticals. Lead MSAT projects and oversee technical studies. 5+ years DP development and aseptic manufacturing expertise required. Collaborative environment, professional growth opportunities.
Procurement support and negotiation for rare disease therapies. 2 years purchasing or finance experience required. Generous time off, conference attendance.
Define and execute commercial strategy for novel targeted therapies in Switzerland. 10+ years pharmaceutical/biotech commercial leadership in oncology, including successful launches, required. Hybrid work, 4-week workation option.
Defining and executing market access strategy for novel oncology therapies in Switzerland. 10+ years of Swiss market access experience in pharma/biotech required. National and international travel, advanced degree in Life Sciences, Pharmacy, Health Economics, or Public Health.
Leading local medical strategy for novel oncology therapies in Switzerland. Advanced degree and 10+ years of oncology medical affairs experience required. Focus on scientific excellence and compliant engagement.
Driving early and late global dermatology programs, including TDP strategies and clinical pharmacology packages. Doctoral degree or MD with board certification in dermatology and 5+ years pharma/biotech experience required. Performance bonus and long-term equity awards.
Developing cost-effectiveness and budget impact models for oncology therapies. 15+ years of economic modeling experience required. Late-stage clinical oncology company context.
Global brand communications strategy for rare disease therapies. Proven healthcare comms/PR experience required. 4-day work week, personal development budget.
Developing clinical pharmacology strategies and PK/PD analyses for rare disease treatments. Ph.D. with 8 years of experience required. Support for regulatory submissions and health authority interactions.
Leading aircraft interior design projects from concept to completion for a global aviation services provider. Minimum 5 years project and budget management experience required. High-profile projects, onsite work.
Developing new auto-injector platforms and prototyping medical devices for a global pharmaceutical company. Mechanical engineering degree and plastic/metal component design experience required. Cross-functional project participation, English technical writing.
Operationalizing strategic projects for a global pharmaceutical company, driving cross-functional teams and senior leadership engagement. Complex project management and drug discovery lifecycle experience required. Performance bonus and long-term equity awards.
Integrating Data42 real world data and human genetics for target identification and patient stratification. 10+ years in human genetics and RWD analytics, including people leadership, required. Performance bonus, global recognition programs.
Translating biological insights into therapeutic and biomarker strategies for oncology programs. PhD and 4+ years of biotech/pharma translational research experience required. Performance-based bonus, global recognition programs.
Defining translational research strategies for oncology programs, driving discovery to clinical translation with cancer biology expertise. PhD and 4+ years of relevant experience required. Performance-based bonus and global recognition programs.
Strategic sourcing and contract negotiation for electromechanical components with third-party suppliers. Bachelor's degree in technical or business field required. Career planning and professional development opportunities.
Developing new neural model methodologies for screening assays and disease modeling. Master’s program enrollment in Life Sciences or related field required. Full accountability for contributions and development.
Global QMS standardization for parenteral production, closing quality systems gaps across manufacturing sites. Specialized manufacturing technology and compliance expertise required. Support for global networks, single point of contact for QMS.
Adapting biochemical and cellular profiling assays for LMW drug discovery, managing LIDO associates. 5+ years' PhD or 10+ years' BSc/MSc experience in assay development required. Fast data turnaround, SOP development, and operational excellence focus.
Developing and adapting biochemical and cellular profiling assays for LMW drug discovery. PhD or MSc with 5-10+ years’ assay development experience required. Fast data turnaround, managing LIDO associates, and SOP development.
Shaping high-impact consulting engagements for life sciences clients. 7-10 years insights and analytics experience required. Focus on Go-to-market strategy and sales force effectiveness.
Instrument qualification for GMP-regulated pharmaceutical manufacturing. Bachelor's degree or equivalent experience with lab instrument qualification and controlled document lifecycle management required. Performance-based compensation programs.
Leading global safety initiatives for neuroscience drug development programs. PhD, PharmD, or equivalent graduate healthcare professional degree required. 4-day work week, company car for private use.
Defining and governing global pharmacovigilance standards for inspection readiness. Senior leadership experience in regulated environments required. Focus on future-state PV process design and platform integration.
Global pharmacovigilance standards definition and governance for patient safety transformation. Senior leadership experience in regulated environments required. Leading future-state PV process design and platform integration.
Leading global safety initiatives for neuroscience drug development. 5+ years clinical and 7+ years drug development experience required. Training and coaching of medical safety physicians and scientists.
Automating thermal denaturation methods in cell systems for lead discovery. Master's degree in life sciences with automation and cell culture knowledge required. Career development support, career opportunities.
Building backend services and robust APIs for text-to-speech products. Backend development with TS/Node and GCP experience required. Bonus, stock options, and autonomy in a dynamic environment.
Delivering cross-platform SDK solutions for audio information platform, optimizing for faster loading. Systems thinking and end-to-end design skills required. Bonus and stock options.
Executing global, regional, and local employee donation and volunteering programs for a global pharmaceutical company. Proven track record in running engagement programs and working with NGOs required. Onboarding beneficiaries into GM&V platforms, 4-day work week.