Medical safety expertise for oncology drug development, including clinical trial protocol contributions and investigator training. MD/PhD and extensive drug safety experience required. Annual bonus and equity.
Steering AR products from idea to out-phasing, coordinating sub-projects, and ensuring alignment across initiatives. Several years of product ownership experience in complex technical environments required. Hybrid work, flexible hours, and talent development opportunities.
Analyzing SaaS recurring revenue and customer movements for real estate software. 2-4 years FP&A or controlling experience required. Hybrid work, BI tool development opportunities.
Developing and validating cell-based and immunoassays for potency in biotech product lifecycle management. 5+ years regulated industry experience required, managerial experience a plus. Flexible hours, digital learning platform.
Selling advanced endotherapy devices to hospitals and healthcare professionals. 2-3 years hospital sales experience required. 30 days holidays, subsidized employee restaurant.
Driving digitalization of quality processes for global medication safety, with GMP-compliant data integrity focus. Several years of experience digitalizing quality in regulated environments required. Hybrid work, flexible hours, talent development.
Leading statistical programming for oncology clinical trials, managing internal teams and external vendors. Oncology experience required. Annual bonus and equity offered.
Leading global audits of clinical investigator sites and vendors for a biotech company. 6 years clinical auditing experience required. Oversight of contracted auditors and resource scheduling.
Leading global safety strategy for new marketing authorizations, including BLA and MAA. Expertise in safety surveillance, signal detection, and risk management required. Focus on scientific excellence and compliance in a biotechnology firm.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Defining validation strategies for clinical systems at a biotech firm. 8+ years in validation/quality, ideally pharma/biotech, required. Focus on regulatory compliance and computer system lifecycle.