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.
Designing and developing robust backend systems for cuffless blood pressure monitoring technology. Deep expertise in Java/Kotlin and AWS cloud services required. Equity program, competitive compensation.
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.
Developing KPI tracking tools for boutique retail excellence. Global environment navigation and team support motivation needed. 7 weeks annual vacation, sports activity financial support.
Developing automated characterization tests for IC blocks and lab infrastructure. 3+ years electronics development and high-precision analog/RF measurements required. Python/C scripting, Altium PCB design.
Developing sub-GHz and 2.4 GHz RF transceiver reference designs for IoT hardware. 3-5 years hands-on hardware design experience required. Company car for private use.
Hands-on support for Semtech RF transceiver silicon and hardware solutions. 3-5 years RF and embedded electronics experience required. Professional development and pay-for-performance culture.
School pickups, homework help, and dinner prep for a school-aged child. Driving license essential, EU passport or Swiss work permit. 4-day work week, 6 weeks vacation.
Defining software and data strategy for cuffless blood pressure monitor technology. Proven leadership in subscription-based, data-heavy businesses required. Equity program participation.
Begutachtung von Fahrzeugschäden und Berechnung von Reparaturkosten für einen Versicherer mit 1,4 Mio. Kunden. Fachausweis als Automobil-Mechatroniker/in oder gleichwertige Ausbildung mit 5 Jahren Erfahrung erforderlich. Französisch als Muttersprache, flexible Arbeitsmodelle.
Leading radio SoC products from concept to market, driving IC design projects. 5+ years microelectronics experience required. 4-day work week, company car for private use.
Pre-silicon RTL verification at block and SoC levels for LPWAN IoT solutions. UVM-based verification methodologies and SystemVerilog proficiency required. Collaboration with design and architecture teams.
Defining and auditing quality processes for biopharmaceutical products, including product integrity testing. 2+ years in pharma with GMP/regulatory familiarity required. French/English proficiency, Veeva Vault experience a plus.