Statistical lead for oncology and infectious disease trials, guiding clinical development plans and regulatory submissions. 15+ years pharma experience with leadership in health authority responses required. Annual bonus and equity.
Leading statistical programming for infectious disease clinical trials, managing SAS deliverables and regulatory compliance. 15+ years of pharmaceutical programming experience required. Annual bonus and equity offered.
Global patient engagement and advocacy for biotech, embedding patient insights into strategic decisions. Minimum 10 years experience in biotech/pharma patient engagement required. People leadership experience with talent coaching and development.
Global quality strategy for packaging, labeling, serialization, storage, and distribution at a biotech firm. 10+ years pharmaceutical QA experience with commercial supply focus required. Flexible hours, vacation account, digital learning.
Driving business development for high-performance glass applications at a global glass manufacturer. Extensive business development or technical sales experience required. Hybrid work, flexible hours.
Managing on-premise and hybrid IT infrastructure services, including compute, storage, and datacenter facilities, for a biotechnology firm. ITIL processes knowledge required. Flexible hours, vacation account, and digital learning opportunities.
Overseeing WAN, LAN, WLAN, VPN, and firewall services for a biotechnology company developing cancer and infectious disease treatments. IT Service Management and ITIL process knowledge required. Flexible hours, vacation account, and digital learning.
Protein pipeline development and analytical coordination for biotech firm. 10+ years biotech/pharma experience with mAbs analytical CMC required. Flexible hours, vacation account.
Computational neuroepigenomics research at a cell nucleus biology institute. Multi-model data integration and machine learning feature prediction required. Supplementary pension scheme, advanced training.
Leading biostatistics for oncology and infectious disease trials, from Phase I-IV. 5+ years leadership experience required. Annual bonus and equity.
Statistical programming for clinical trials in oncology and infectious diseases. Advanced degree and 5+ years in pharma/CRO required. Collaboration with global programming standard library development.
Technical leadership for upstream/downstream processing and harmonization efforts at a global biotechnology firm. 6+ years of experience in bioprocessing and chromatography required. Flexible hours, vacation account, and digital learning opportunities.
Statistical lead for oncology/infectious disease clinical trials, ensuring accuracy for regulatory submissions. 8 years of pharma/CRO experience with leadership required. Annual bonus and equity offered.
Financial modeling and valuation for global M&A transactions at bulge bracket investment bank. Corporate finance specialization and prior investment banking experience required. Consultation for life situations, mental health awareness trainings.
Ensuring IT system compliance with global health authority regulations for a biotechnology firm. 5+ years pharmaceutical industry and regulated IT quality experience required. Flexible hours, vacation account, digital learning.
Digitalizing quality engineering processes for global medication use, ensuring GMP data integrity. Bachelor's degree and 3-5 years in GMP quality engineering required. Flexible working hours, hybrid work, and public transport access.
Optical coating simulations and AR waveguide design for high-volume production. 7+ years thin film experience and simulation tool proficiency required. Flexible hours, company pension, and talent development.
Owning specific L2C sub-processes for a biotechnology company, driving operational excellence with S/4HANA implementations. 5+ years in multinational L2C/O2C environments required. Flexible hours, vacation account.
Analyzing pharmacovigilance and medical data for benefit-risk assessments at a biotech firm. Master's degree and SQL/Python or R proficiency required. Flexible hours, vacation account.
SAP S/4HANA finance process integration for biotech, supporting end-to-end pharma processes. 5+ years SAP finance integration experience required. Collaboration with IT and business leads, documentation review.
Overseeing GxP-compliant pharmaceutical manufacturing operations globally and aligning with clinical objectives. Extensive GxP and pharmaceutical manufacturing experience required. Flexible hours, vacation account, digital learning.
Developing AR waveguide and component concepts with Python-based optical simulation tools. MS in Optical Engineering or equivalent experience required. Flexible working hours, active health management.
Translating corporate strategy into inspiring messaging for a biotech firm. Strategic thinking and business-critical situation management required. Flexible hours, vacation account, and leadership development.
Analyzing business demand and aligning core capabilities with Enterprise Architects for a biotech firm. Proven track record in customer engagement systems, Veeva Vault knowledge required. Flexible hours, vacation account.
Practical research in CRISPR/Cas genome editing, NGS, and gene network modeling for epigenetics and RNA biology. Current Bachelor's or Master's student status essential. Access to lectures and seminars by leading scientists.
Developing sourcing strategies and supply pipelines for used, new, and surplus batteries on a B2B marketplace for battery reuse/recycling. Comfort with battery fundamentals and B2B agreement negotiation skills essential. Structured tracking in CRM and sourcing tools.
Developing supply partnerships for used EV and energy storage batteries on a B2B marketplace. 3-8+ years in sourcing or procurement for battery/industrial supply chains required. Flexible working hours, hybrid remote model.
Leading analytical project strategy for antibody development across interdisciplinary teams. 10+ years biotech/pharma industry experience, strong analytical CMC background required. Flexible hours, vacation account.
Defining rendering system vision and leading a 3D programming team for original gaming experiences at a global game developer. Leadership in 3D environments and excellent C/C++ real-time rendering skills required. Relocation financial support, accommodation search, and visa assistance provided.
Designing MAH/Sponsor process landscapes and advising on complex GMP matters in pharmaceutical manufacturing. 3+ years experience in GMP Compliance, QMS, and MAH/Sponsor processes required; advanced QM/RA certifications a plus. Vacation account, flexible hours.