Designing and executing analytical methods for Oligonucleotides in drug substance and product development. Strong Oligonucleotide analytics experience required. Performance-based bonus, global recognition programs.
Designing and executing analytical methods for Oligonucleotides in pharmaceutical R&D. Prior experience in oligonucleotide analytics required. Performance-based bonus, global recognition programs.
Defining product strategy and roadmap for AI-driven pharma cold chain operations. Proven pharma supply chain product management experience required. Hybrid workplace, flexible hours.
Method validation and stability studies for biological drugs at a biopharmaceutical company. MSc/PhD and experience with HPLC, ELISA, and CMOs required. 4-day work week, personal development budget.
Global pharmacovigilance process development and regulatory reporting for oncology therapies. 10+ years in PV with leadership experience required. EU QPPV compliance, advanced degree in Medicine or Pharmacy.
Advancing 3D-Electron Diffraction applications for pharmaceutical compounds. Expertise in structure determination using 3D-ED required. Access to advanced technologies, global community.
Leading calibration for drug substance at global healthcare innovator. Developing and implementing calibration procedures, ensuring regulatory compliance. Collaboration with cross-functional teams, maintaining records and documentation.
Global patient safety surveillance for oncology therapies, leading a team and designing core processes. Advanced degree and 12+ years in PV, with 6+ years people management, required. Focus on process quality and regulatory document consultation.
Developing Asset Administration Shell (AAS) solutions for production process optimization at a global healthcare company. Master's degree enrollment in digitalization or engineering required. 12-month internship with 50% salary.
Hands-on in vivo research support, including compound administration and sample collection for drug discovery. Bachelor's degree with 7+ years of in vivo study experience required. LTK1 certification or equivalent needed. Daily clinical observations, study design contributions.
Hands-on in vivo research support, including compound administration and sample collection for drug discovery. Bachelor's degree with 7 years of in vivo studies experience required. LTK1 Certification or equivalent needed. Study design contribution, clinical observations, and recent PhDs considered.
Leading a drug discovery biology lab for oncology therapeutics. Ph.D. in cancer biology or related field required. Performance-based bonus, long-term equity awards.
Launch preparation for daraxonrasib and future GI compounds in oncology. 8+ years biotech/pharma marketing experience in European markets required. Collaboration with cross-functional teams, project management capabilities.
Developing and validating in vitro cell culture assays for therapeutic projects. Apprenticeship as biology laboratory technician required. Delivering high-quality data for regulated and non-regulated toxicology assays.
Designing and optimizing in vitro toxicology assays for drug safety prediction. Master's degree and PhD in immunology with 2+ years postdoctoral experience required. Support in vitro predictive safety model development.
Formulating integrated immunosafety strategies and championing scientific validation of predictive immunological biomarkers. PhD in immunology-related field and strong industry focus on in vitro/in vivo human immunology required. Upgrading predictive cell models (2D, 3D, microphysiological systems), 4-week workation option.
Developing advanced biomarker assays and implementing epigenetics/gene expression signatures for pharmaceutical research. Deep proficiency in molecular biology techniques and NGS platforms required. Hands-on laboratory work with digital tools in a 500+ employee life sciences organization.
Defining the 'Golden Form' for drug candidates through solid-state characterization and crystallization. Ph.D. in Pharmaceutical Sciences, Chemistry, or Material Science required. Personal and professional thriving, culture of curiosity.
Leading quantitative clinical pharmacology for drug development programs using Model-Informed Drug Development (MIDD) approaches. 5+ years in pharma/biotech quantitative clinical pharmacology required. Personal expression encouraged, open dialogue fostered.
Unifying outsourced drug discovery workflows with premier CROs and tech partners. Minimum 5 years managing external partnerships in pharma required. Personal and professional thriving, open dialogue encouraged.
Designing specialized oral formulations to maximize drug exposure for novel synthetic molecules. PhD in Pharmaceutical Technology and 8+ years industry experience required. Technical network establishment, global strategy development.
Developing integrated hematology and safety biomarker strategies with wet-lab assay execution for clinical candidate selection. DVM (PhD/specialization) or PhD in relevant science required. Focus on optimizing lab processes and mentoring scientific talent.
Developing and validating pathology investigations using computational approaches for Roche. Board-certified veterinary pathologist with toxicologic pathology experience required. Culture of curiosity, personal expression, and open dialogue.
Designing and optimizing therapeutic siRNAs for various disease targets, integrating computational and empirical approaches. Deep understanding of RNAi mechanism and siRNA profiling required. Focus on AI engineer collaboration and advanced chemical modification patterns.
Developing and validating bioanalytical methods with HPLC and mass spectrometry for small molecules, peptides, and oligonucleotides. MSc or PhD in bioanalysis or related field required. Automation and digitalization initiatives to increase sample throughput.
Conducting forensic chemistry studies with light microscopy, FTIR, and Raman spectroscopy. Bachelor's or Master's degree in a science field required. Agile career path, dynamic work culture.
Supporting purchasing of materials, tooling, and equipment for over 35 aircraft types. Monitoring internal and external loan tools required. Tripartite internship agreement, English proficiency needed.
Developing and validating quantitative LC-MS/MS methods for drug candidates and biomarkers. Advanced analytical techniques and computerized data acquisition systems experience required. Support for non-clinical PK/TK and exploratory clinical studies.
Leading clinical pharmacology and MIDD strategies for drug development. Quantitative clinical pharmacology expertise required. Focus on computational methodologies and regulatory approvals.
Purchasing aircraft parts and tooling for line maintenance supporting 35+ aircraft types. Proven purchasing and warehouse experience with aircraft parts handling required. Professional and personal development opportunities.