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.
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.
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.
Leading teams in assessing financial statements and issuing auditor's reports at a global professional services firm. Strong knowledge of accounting and financial reporting standards essential. Focus on team development and client engagement.
Designing advanced wireless communication algorithms for high-end semiconductors at a mixed-signal chip supplier. Master's or PhD in Electrical/Computer Engineering with expert communication theory knowledge required. Algorithm prototyping using MATLAB, Python, C/C++.
Managing daily building operations, security, and maintenance technician coordination for an engineering office. Proficiency in MS Office and SAP, with administrative organization and filing experience required. Flexible working pattern.
Preparing product quality reviews and regulatory documentation for therapies in GI, oncology, and rare diseases. 3-5 years biotech/pharma manufacturing experience with eCTD license review essential. 28 days PTO, sport/fitness contribution, preventive healthcare support.
Leading Lean/Six Sigma projects and designing future factory processes for biopharmaceutical production. Master's degree in technical fields and 8+ years manufacturing/operations experience required. 28 days paid time off, Sport/Fitness abonnement contribution, preventive healthcare support.
Leading small molecule API manufacturing sciences, applying mechanistic modelling for batch/continuous platforms in biopharmaceutical production. Master's in Chemical/Process/Pharm Engineering and 5+ years small-molecule production experience in cGMP required. Work across both batch and continuous manufacturing platforms.
Kundenberatung zu Brillen, Kontaktlinsen, Hörsystemen im drittgrößten Augenoptik-Unternehmen. Freude am Umgang mit Menschen und Gespür für Mode/Trends erforderlich. 13. Gehalt, SBB-Generalabonnement, Mitarbeiteraktien.
RF front end design and optimization for analog/mixed-signal semiconductors powering high-end consumer and industrial tech. 7+ years semiconductor industry experience with LNA, mixer, filter, PA expertise needed. Hybrid working model, 100% salary during sick leave.
Design, simulate, and optimize radio circuits and matching networks for semiconductor products. Hands-on expertise in LNAs, mixers, filters, and EM simulation tools (HFSS, EMX) essential. Loyalty bonus scheme, 100% salary during sick leave.
Strategic tax consulting and compliance for high-profile corporate clients at an international tax advisory firm. Swiss tax expert diploma preferred, fluent French and English needed. Diverse, international work environment.
Producing and testing precise time distribution systems for communication networks. Federal Certificate in electronics/electrotechnics or equivalent, industrial production experience needed. Awarding for implementing new ideas.
Customer assistance, product packaging, and merchandise restocking at a crystal and jewelry brand. Retail experience preferred, with flexibility for Friday and Saturday shifts needed. Swarovski product discounts.
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.
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.
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.
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.