Leading clinical development strategies and managing physicians for novel oncology drugs. At least 10 years of MD experience required. Work-life balance programs, employee resource groups.
Quality oversight for CMOs, including disposition documentation and cGMP compliance. Strong technical expertise in deviation resolution and risk assessments required. 4-day work week, company car for private use.
Managing European IP for small/large molecule patents and EP oppositions. Patent litigation experience preferred. Work-life balance programs, employee resource groups.
Leading EU demand planning for a global biopharma company, managing a team of planners. 10-15 years supply chain planning experience in pharma/consumer goods required. 4-day work week, company car for private use.
Updating legacy calibration documents and creating new WIs/SOPs for pharmaceutical operations. Technical discipline formation with quality or metrology domain experience required. Internship at a global biopharmaceutical company.
Manufacturing finance for a new pharmaceutical launch facility, advising on CAPEX and project accounting. Qualified accountant with strong manufacturing cost accounting knowledge required. No distinguishing benefits provided in input.
End-to-end logistics management across all modalities for major EU markets and complex Middle East distribution hubs. Minimum 15 years of experience in market supply operations or pharmaceutical logistics required. Cross-market distribution oversight, regional supply point management.
Ensuring robust manufacturing processes and technical readiness for new pharmaceutical product launches. Advanced degree in Pharmaceutical Sciences or Engineering, 8+ years pharma manufacturing experience, and French/English fluency required. International environment with global clinical trial participation.
Shaping launch excellence and growth strategies for clinical science across European markets, fostering cross-market collaboration at a clinical research organization. Over 10 years commercial operations experience with European market understanding desired. Fostering a strong S&O community, direct impact on patient outcomes.
EHS program leadership and compliance for global clinical trial operations. Fluency in French and English required. Collaboration with global EHS community and site teams.
Constructing knowledge graphs and designing query interfaces for clinical trial data at a biotech firm. MSc in Data Science or similar, with strong Python proficiency, required. Integrating machine learning techniques.
Emulating target trials using real-world datasets for global clinical trials. Master's or Ph.D. in statistics/epidemiology required; R/SAS proficiency preferred. Direct involvement with a global clinical trials team, gaining real-world data analysis experience.
EHS compliance and program leadership for new Process Unit launches at biotech firm focused on clinical trials. Relevant permits for OSD manufacturing facility required. Impacting global clinical trials through critical program leadership.
Lab equipment use for raw material and finished product analysis in GMP environment for clinical trials. Aptitude in math/science and basic English knowledge required, minors welcome. Exposure to global clinical trial processes.
Local sourcing for capital projects, equipment, and MRO/OEM within a biopharmaceutical manufacturing network. cGMP experience in biopharma or medical device industry required. Global network engagement with sister sites.
Local sourcing leadership for global clinical trials and biopharmaceutical manufacturing. cGMP experience in biopharma/med device and SAP/Ariba expertise required. Cross-functional engagement within a global manufacturing network.
Equipment validation and qualification for clinical trial operations, applying cGMP and risk-based C&Q strategies. 1+ year pharmaceutical industry experience and cGxP knowledge required. Global clinical trial focus.
Qualification and cleaning validation projects within a pharmaceutical MS&T team, applying DMAIC for process improvement. Master's or PhD student in Pharmaceuticals, with solid oral dosage forms knowledge, required. Exposure to global clinical trial context.
Troubleshooting and optimizing production equipment in pharmaceutical manufacturing. 10 years industrial maintenance experience and GMP environment knowledge required. Work in a strictly regulated GMP environment.
Leading complex multi-national clinical trials at a science-driven organization, ensuring data quality and regulatory compliance. 10+ years in clinical operations and global project management, with Director-level global trial leadership, required. Strategic leadership for global clinical programs.
Overseeing purchase order lifecycle for clinical trial supplies, including QA release. 3 years experience in supply chain operations, pharmaceutical environment, and GMP required. International collaboration in a dynamic supply chain.
Supporting automated production system development for connectivity and sensor solutions. Basic LabVIEW and C# programming skills required. Practical industrial experience, performance bonus, and diverse project exposure.
Tax advisory for diverse clients, focusing on planning, compliance, and strategy. High performance habits and feedback skills required. Working with varied clients and team members.
Führen von Bauzügen unter Einhaltung von Sicherheitsvorschriften und Arbeitsprozessen. Abgeschlossene Berufslehre (EFZ) in technischem Bereich und Führerausweis Kategorie B zwingend. Kostenloses GA 2. Klasse, 16 CHF Stundenlohnzusatz für Sonntagsarbeit.
Designing automated data pipelines and Power BI solutions for biopharmaceutical production sites. Experience in GMP and IT/OT environments required. 28 days PTO, fitness contribution, on-site cafeteria.
Building and improving integrations for cuffless blood pressure monitors. 5+ years in automation with Make, Zapier, or n8n required. Autonomous execution of technical integrations.
Quality engineering for continuous blood pressure monitor manufacturing with contract partners. ISO and FDA QSR knowledge required. Flexible work location, hybrid schedule, occasional international travel.
Leading OT automation projects for biopharmaceutical production, managing lifecycle of equipment and systems. Industrial IT/Automation OT degree and GMP environment knowledge required. 28 days PTO, sport abonnement contribution, on-site cafeteria.
Designing, simulating, and optimizing baseband and RF blocks for IoT solutions. Master's degree with 3+ years' semiconductor experience required. Collaborative engineering environment, pay-for-performance culture.
RF front end design, simulation, and optimization for semiconductors. Master’s degree and expertise in LNAs, mixers, and filters required. Collaborative engineering environment, pay-for-performance culture.