Solvias AG

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    "title": "Metrology Specialist",
    "description": "Job opening — Metrology Specialist | Solvias AG | Kaiseraugst.\n\nYour day-to-day tasks will cover:\n\n• Take ownership of core responsibilities within your area of expertise\n• Collaborate with cross-functional teams to achieve shared goals\n• Maintain quality standards and adhere to internal processes\n\nWe are looking for someone with:\n\n• Hands-on experience in laboratory equipment handling, maintenance and troubleshooting\n• Experience in GMP regulated environment is an plus\n• Strong technical interest, ideally with an affinity to IT systems\n• Excellent communication skills and team-oriented mindset\n• Relevant degree and professional experience\n• Strong communication and teamwork skills\n\nWhat we offer:\n\n• Competitive salary package\n• Flexible working arrangements\n• Career development opportunities\n\nDon't miss this opportunity — join Solvias AG and take your career further.",
    "datePosted": "2026-06-11",
    "validThrough": "2026-07-11",
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    "title": "Senior Analytical Manager Pharmacopeia Solutions",
    "description": "Solvias AG recrute un(e) Senior Analytical Manager Pharmacopeia Solutions a Kaiseraugst.\n\nAs Senior Analytical Manager for our Pharmacopeia Solutions team, you lead a laboratory group responsible for compendial and routine analytical testing, including titration, raw material testing, and water content analysis (Karl Fischer).\nYou ensure efficient, compliant, and high-quality execution of analytical activities, while driving team performance, operational excellence, and continuous improvement within a GMP-regulated environment.\nLeadership & Team Management:\n•\nLead, coach, and develop a team of scientists and laboratory personnel\n•\nEnsure effective resource allocation and capacity planning\n•\nDrive performance management, training, and career development\n•\nSupport recruitment and onboarding activities\nOperational Excellence in Pharmacopeial Testing:\n•\nOversee routine analytical testing (titration, raw material testing, Karl Fischer)\n•\nEnsure timely and reliable delivery of analytical results\n•\nOptimize workflows for high-throughput environments\nQuality, Compliance & Data Integrity:\n•\nEnsure compliance with GMP and pharmacopeial standards (Ph. Eur., USP)\n•\nMaintain strong data integrity and inspection readiness\n•\nLead audits and quality investigations\n•\nEnforce HSE standards\nProcess Improvement:\n•\nDrive continuous improvement and standardization\n•\nSupport digitalization and automation initiatives\nTechnical & Stakeholder Support:\n•\nAct as subject matter expert for pharmacopeial methods\n•\nSupport troubleshooting and client interactions\nFinancial & Strategic Contribution:\n•\nSupport budget planning and cost control\n•\nContribute to strategy and service expansion\nEducation & Background:\n•\nMSc or PhD in Chemistry, Pharmaceutical Sciences or related field\n•\nSeveral years of experience in GMP-regulated laboratories\n•\nProven leadership experience\nTechnical Skills:\n•\nParcours professionnel in pharmacopeial testing\n•\nStrong knowledge in titration, raw material testing, Karl Fischer\n•\nUnderstanding of Ph. Eur. / USP\nLeadership & Personal Skills:\n•\nStrong leadership and coaching skills\n•\nStructured, solution-oriented mindset\n•\nExcellent communication and stakeholder management\n•\nHigh quality and ownership mindset\n\nRejoignez Solvias AG et donnez un nouvel elan a votre carriere.",
    "datePosted": "2026-06-06",
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    "title": "Scientist - Analysis and Biophysical Characterization of Biomolecules - 100% - f/m/d",
    "description": "Poste a pourvoir : Scientist - Analysis and Biophysical Characterization of Biomolecules - 100% - f/m/d -- Kaiseraugst -- Solvias AG.\n\nWe are looking for a motivated analytical scientist with a background in biochemistry, analytical sciences, or a related field and a passion for optical spectroscopy. If you thrive in a GMP/ISO-regulated biopharmaceutical environment, enjoy working with precision and teamwork, and bring a hands-on, detail-oriented mindset, we'd love to hear from you.\nBecome part of our team and contribute to meaningful work in biopharmaceutical drug development -- we look forward to getting to know you!\n•\nAnalytical testing for customer projects in the area of biopharmaceutical molecules (proteins/peptides) and ATMPs (LNPs, AAVs, RNA) with focus on optical spectroscopy.\n•\nComplement with scientific knowledge for relevant techniques such as AUC, FTIR, CD, DLS, SEC/AF4-MALS, Polarimetry, nanoDSC, UV Absorbance, Fluorescence.\n•\nAnalysis of customer samples, documentation and preparation of analytical results and support/guidance in a team of ca. 12 colleagues (technicians and scientists).\n•\nResponsibility for instruments in a qualified environment including performance of periodic tests, organization of maintenance.\n•\nEnsure analytical activities align with health, safety, environmental and GMP/ISO 9001 quality standards.\n•\nSupport quality management tasks (e.g. QE, OOS, CR) and organize/execute projects adhering to GMP/ISO 9001 quality standards.\n•\nEducational background in biochemistry, analytical sciences or a related field with focus on optical spectroscopy.\n•\nIndustry experience (>2 years) in biopharmaceutical drug development environment, with a strong background in GMP/ISO-regulated analytical testing is advantageous.\n•\nStrong communication, organization and planning skills.\n•\nIndependent, detail-oriented work style and a team-oriented attitude.\n•\nProficiency in MS Word and Excel.\n•\nFluent in English (additionally German and/or French is beneficial)\n\nNe laissez pas passer cette offre -- postulez maintenant.",
    "datePosted": "2026-05-30",
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    "title": "Commercial Analyst",
    "description": "Solvias AG ouvre un poste de Commercial Analyst a Kaiseraugst.\n\nSolvias is a global provider of chemistry, manufacturing, and control (CMC) analytics to the life sciences industry. Our expert team combines decades of background with regulatory expertise across small molecules, biologics, and cell and gene therapies. Solvias offers end-to-end solutions from raw material testing to drug product release and API development for small molecules. Headquartered near Basel, Switzerland, Solvias operates six global Centers of Excellence, all adhering to the highest ISO, GMP, GLP, and FDA standards\nCommercial Analyst\nThe Commercial Analyst supports the commercial organization within a CRO environment by delivering data-driven insights on sales performance, pipeline development, and customer activity. This role is critical in managing KPIs, improving forecast accuracy, and ensuring transparent and accurate sales incentive calculations. The position works closely with Business Development, Finance, and Operations teams to drive profitable growth and optimize commercial performance.\nSales & Pipeline Analysis\n•\nAnalyze sales performance, order intake, and revenue trends across customers, projects, and therapeutic areas\n•\nMonitor and evaluate the commercial pipeline using Salesforce data (opportunities, conversion rates, cycle times)\n•\nProvide insights on business development performance and project progression\nKPI Management & Reporting\n•\nDefine, track, and report key commercial KPIs (e.g., pipeline value, win rates, revenue, margin, project lifecycle metrics)\n•\nDevelop and maintain interactive dashboards and reports in Power BI\n•\nEnsure alignment and consistency of KPIs across commercial and finance teams\nSales Incentives Management\n•\nCalculate and validate sales incentives based on defined compensation plans\n•\nTrack individual and team performance against targets\n•\nCollaborate with Finance and HR to ensure accurate and timely incentive payouts\nForecasting & Commercial Planning\n•\nDevelop and maintain sales and revenue forecasts based on pipeline data and historical trends\n•\nPartner with Business Development and Project Management teams to assess probability and timing of deals\n•\nSupport budgeting, S&OP inputs, and long-term commercial planning\nCRM & Data Governance (Salesforce)\n•\nEnsure data quality, completeness, and consistency in Salesforce CRM\n•\nSupport users in maintaining accurate pipeline and customer data\n•\nIdentify and implement improvements in CRM usage and reporting structures\nBusiness Partnering & Insights\n•\nProvide ad hoc analysis on pricing, margins, customer profitability, and project performance\n•\nSupport strategic initiatives such as account planning and portfolio optimization\n•\nTranslate complex data into clear insights and recommendations for senior stakeholders\n•\nBachelor's degree in Business Administration, Finance, Data Analytics, or related field\n•\n3-6 years of parcours professionnel in commercial analysis, sales operations, or business analytics\n•\nExperience in CDMO, pharma, biotech, or life sciences industry strongly preferred\n•\nAdvanced Excel skills (data modeling, pivot tables, complex formulas)\n•\nHands-on parcours professionnel with Salesforce CRM (reporting, pipeline analysis, data management)\n•\nExperience with Power BI is a plus (dashboard creation, data modeling, DAX)\n•\nAbility to analyze complex datasets and generate actionable insights\n•\nExperience with forecasting methodologies and KPI frameworks\n•\nStrong attention to detail and data accuracy\n•\nAbility to work cross-functionally (Business Development, Finance, Operations)\n•\nProactive mindset with strong organizational skills\n\nSaisissez cette opportunite et postulez des aujourd'hui.",
    "datePosted": "2026-05-12",
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    "title": "Associate Director ELISA / SPR / Cell-based bioassays",
    "description": "Poste a pourvoir : Associate Director ELISA / SPR / Cell-based bioassays -- Kaiseraugst -- Solvias AG.\n\nLead a high-performing analytical lab team driving cutting-edge bioanalytical CMC testing (ELISA, SPR, cell-based assays) in GMP-regulated drug development. Shape operations, inspire people, and deliver scientific excellence while partnering closely with customers and senior leadership.\n•\nLead an analytical lab operations team, focusing on providing services incl. ELISA, SPR and Cell-based bioassay testing in the context of CMC analytical drug development\n•\nPersonnel management of multiple Analytical Managers, Scientists, Lab Technicians and ensure high-performance team execution\n•\nDefine priorities across lab sub-areas, ensuring effective workload distribution\n•\nOversee laboratory capacity planning, recruitment, and career development\n•\nPromote a culture of collaboration, accountability, and operational excellence\n•\nEnsure budget adherence and cost-efficient operation of laboratories\n•\nIdentify opportunities for cost-saving and process optimization\n•\nAct as the primary liaison between the analytical team and senior leadership\n•\nRepresent the company in interactions with customers\n•\nEnsure all analytical activities align with health, safety, environmental and GMP/ISO 9001 quality standards\n•\nDrive continuous improvement initiatives to enhance compliance and efficiency\n•\nLead audit preparations and interactions, CAPA implementations\n•\nBackground in CMC bioanalytical drug development testing (ELISA, SPR, Cell-based bioassays) under GMP\n•\nEducational background in biochemistry, analytical sciences or a related field\n•\nIndustry experience (>5 years) in biopharmaceutical drug development environment, with a strong background in GMP/ISO-regulated analytical testing\n•\nProven industry leadership background\n•\nExpertise in regulatory compliance, analytical method development, and operational excellence\n•\nDemonstrated ability to drive continuous improvement in analytical workflow processes\n•\nHigh-level problem-solving, conflict resolution, and decision-making skills\n•\nStrong ability to engage with customers\n•\nStrong communication skills\n•\nFluent in English (additionally German is beneficial)\n\nPostulez des maintenant pour ce poste de Associate Director ELISA / SPR / Cell-based bioassays a Kaiseraugst.",
    "datePosted": "2026-04-30",
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    "title": "Scientist - Pharmacopeia Solutions (m/w/d)",
    "description": "As Scientist for the current position, you will act as the key liaison between the laboratory team and the Analytical Manager, ensuring seamless communication and technical alignment across all analytical operations. Your function will involve both administrative tasks as well as experimental, analytical lab work as described in detail under responsibilities.     Method Development & Validation: Independently plan and execute method development and validation projects, including the preparation and approval of all required GMP documentation (SOPs, protocols, and reports).    Analytical Execution: Perform and oversee analyses in classical CHNSO combustion and TOC analytics (including TNb, swab extraction and cleanability studies) within the framework of cleaning validations, as well as titration and potentiometric techniques (e.g., Karl Fischer, Argentometry, ISE).    Operational Support: Provide hands-on assistance and expert troubleshooting for daily laboratory operations, with a proactive approach to taking ownership of advanced analytical challenges and inquiries.    Project & Quality Management: Ensure the timely completion of projects, delivering high-quality results that meet or exceed client expectations through effective self-management and rigorous attention to detail.    Compliance & Organisation: Maintain meticulous, GMP-compliant documentation and archiving of all laboratory activities while assisting with organisational tasks to ensure smooth and efficient lab workflows.    Instrument Stewardship: Take charge of analytical instrumentation, ensuring data integrity, performing routine management/maintenance and coordinating with external suppliers as required.     Degree in chemistry, pharmacy, biology or a related field in the natural sciences   Proven hands-on experience in the analytical techniques mentioned above, including proficiency in relevant sample preparation methods.   Prior experience handling quality related topics (quality events, changes, deviations, OOS) is considered a distinct advantage.   Experience in quality events, change requests, deviations or out-of-specification process and documentation is advantageous   Proactive with a can-do attitude and very good communication skills and scientific writing skills   Advanced skills in MS Office (Word, Excel, PowerPoint) and basic experience with LIMS (e.g., LabWare) are considered a plus   Professional experience within a GMP-regulated environment is highly desirable.   Dedicated team player with a strong service-oriented mindset and a high sense of responsibility.   Fluency in English (both written and spoken) is required; knowledge of German is a beneficial asset.   ",
    "datePosted": "2026-04-23",
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    "title": "Lab IT Administrator",
    "description": "Solvias is a global provider of chemistry, manufacturing, and control (CMC) analytics to the life sciences industry. Our expert team combines decades of experience with regulatory expertise across small molecules, biologics, and cell and gene therapies. Solvias offers end-to-end solutions from raw material testing to drug product release and API development for small molecules. Headquartered near Basel, Switzerland, Solvias operates six global Centers of Excellence, all adhering to the highest ISO, GMP, GLP, and FDA standards Lab IT Administrator  Oversee the administration and functionality of laboratory systems and applications, including onboardings, regular updates and troubleshooting Collaborate with IT, Quality, and vendors to resolve complex technical issues Write and review documents related to laboratory systems and applications (for example qualifications, SOPs) Support planned changes, deviations, CAPA Support IT systems and infrastructure Ensure laboratory software and systems are functioning efficiently, performing upgrades as needed Provide technical support for laboratory personnel using scientific applications Troubleshoot common issues, offer solutions, and escalate complex issues to the IT team when required Maintain documentation on system configurations, troubleshooting guides, and procedures Monitor and check compliance laboratory systems and applications with (internal) regulations, as well as the higher-level / official regulations and guidelines (ISO 9001, GMP) Assist with customer audits and regulatory authority inspections   Excellent interpersonal and customer service skills Ability to communicate effectively with laboratory personnel to identify IT needs, provide timely IT solutions and adapt to shifting priorities Familiarity with GMP regulations, data integrity, and quality requirements Knowledge of scientific applications, such as Chromeleon, and their troubleshooting processes Experience in IT infrastructure Experience with system integration and optimization in a laboratory setting Strong organizational skills with a focus on maintaining accurate documentation ",
    "datePosted": "2026-04-01",
    "validThrough": "2026-06-30",
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