You are a Category and sourcing subject matter expert in External Manufacturing of pharmaceutical productsConducting market and internal analysis to develop strategies, best practices, and guidance on tactical plans for how Roche should source and negotiate for third party goods and services in order to satisfy stakeholder requirements and maximize the value for RocheYou are a Procurement delivery practitioner delivering and executing sourcing strategies and major initiatives by leveraging spend, category know-how, robust sourcing, negotiation, contracting, supplier management methodologies and project management skills and/or supporting team members by coaching them and enhancing their skills and knowledgeYou develop content and automation, translating sourcing strategy into content and automated buying channels guidelines, best practices and communication materials that improve business adoption, satisfaction, and overall efficiency Deep expertise in CDMO sourcing for Drug Product and Finished Goods Manufacturing, with strong understanding of global market dynamics and cost drivers Proven experience in strategic sourcing and complex contract negotiations, including long-term CDMO agreements and capacity modelsStrong knowledge of GMP and regulatory requirements (e.g., FDA, EMA) and their impact on supplier selection and contractingDemonstrated ability to develop and execute category strategies aligned with business needs, supply security, and value deliveryExperience in cross-functional stakeholder management, effectively collaborating with Quality, Regulatory, and Technical Operations in a global environment Solid track record in supplier relationship and performance management, driving continuous improvement and risk mitigationProficiency in procurement tools (e.g., SAP Ariba) and data-driven decision making, including translating strategies into automation and buying channel guidanceExcellent communication and influencing skills in English, with the ability to simplify complex topics and support team capability buildingYou have an expert understanding of the CDMO market for Drug Product and Finished Goods ManufacturingYou have a good understanding about the GMP and regulatory requirements and their impact on CDMO Procurement StrategiesYou have very good communication skills, especially in English and you are an expert in pro-active stakeholder management, being used to work in a remote environment World-renowned pharmaceutical company Internal career opportunities Ihr Kontakt Referenznummer 871308/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Act as Analytical SME / Analytical Project Lead (APL), driving development of analytical control packages for synthetic molecules (APIs, intermediates, IPCs)Develop and optimize analytical methods using advanced techniques (HPLC, UHPLC, MS, GC).Contribute to process development analytics, including modern approaches like modeling and simulationCoach and support technicians and junior scientists, acting as a central project contactOversee laboratory activities and manage external testing with CDMOs/CLOsCollaborate cross-functionally with R&D, Regulatory, and Quality teams to ensure smooth project executionAuthor, review, and approve regulatory documents and dossiers (e.g., QIMPD, NDA) ensuring compliance and data integrity Advanced degree (Master’s/PhD) in Chemistry, Pharmacy, or related fieldSolid experience in analytical development of synthetic drug substancesDeep expertise in liquid chromatography (HPLC/UHPLC) and detection methods (MS, UV, fluorescence, CAD)Strong knowledge of analytical chemistry techniques (chromatography, titration, physicochemical methods)Proven leadership skills in project coordination, technical supervision, and mentoringStrong digital and analytical mindset, including data analysis and statistical evaluationExcellent communication skills in English with strong cross-functional collaboration abilities Opportunity to lead high-impact analytical development activities across clinical and commercial drug projectsExposure to cutting-edge analytical technologies within a global pharma R&D environmentStrong potential for contract extension and growth within a world-class technical development organization Ihr Kontakt Referenznummer 879651/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
You are a Category and sourcing subject matter expert in External Manufacturing of pharmaceutical products Conducting market and internal analysis to develop strategies, best practices, and guidance on tactical plans for how Roche should source and negotiate for third party goods and services in order to satisfy stakeholder requirements and maximize the value for Roche You are a Procurement delivery practitioner delivering and executing sourcing strategies and major initiatives by leveraging spend, category know-how, robust sourcing, negotiation, contracting, supplier management methodologies and project management skills and/or supporting team members by coaching them and enhancing their skills and knowledge You develop content and automation, translating sourcing strategy into content and automated buying channels guidelines, best practices and communication materials that improve business adoption, satisfaction, and overall efficiency Deep expertise in CDMO sourcing for Drug Product and Finished Goods Manufacturing, with strong understanding of global market dynamics and cost drivers Proven experience in strategic sourcing and complex contract negotiations, including long-term CDMO agreements and capacity models Strong knowledge of GMP and regulatory requirements (e.g., FDA, EMA) and their impact on supplier selection and contracting Demonstrated ability to develop and execute category strategies aligned with business needs, supply security, and value delivery Experience in cross-functional stakeholder management, effectively collaborating with Quality, Regulatory, and Technical Operations in a global environment Solid track record in supplier relationship and performance management, driving continuous improvement and risk mitigation Proficiency in procurement tools (e.g., SAP Ariba) and data-driven decision making, including translating strategies into automation and buying channel guidance Excellent communication and influencing skills in English, with the ability to simplify complex topics and support team capability building You have an expert understanding of the CDMO market for Drug Product and Finished Goods Manufacturing You have a good understanding about the GMP and regulatory requirements and their impact on CDMO Procurement Strategies You have very good communication skills, especially in English and you are an expert in pro-active stakeholder management, being used to work in a remote environment World-renowned pharmaceutical company Internal career opportunities Ihr Kontakt Referenznummer 871308/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Perform all pull (retrieval, labelling and documentation) activities for stability studies Login and receive samples in LIMS Close collaboration with different departments Perform all staging (Packaging, labelling, documentation) activities Collect and keep updated data in LES (Laboratory Execution System) system Organize storage of boxes in stability chamber in close collaboration with different departments Support the improvement of the sample management process Ensure safety and health protection by following lab and safety instructions and all cGMP regulations Perform other duties as assigned A degree in e.g.
Act as Analytical SME / Analytical Project Lead (APL), driving development of analytical control packages for synthetic molecules (APIs, intermediates, IPCs) Develop and optimize analytical methods using advanced techniques (HPLC, UHPLC, MS, GC).Contribute to process development analytics, including modern approaches like modeling and simulation Coach and support technicians and junior scientists, acting as a central project contact Oversee laboratory activities and manage external testing with CDMOs/CLOs Collaborate cross-functionally with R&D, Regulatory, and Quality teams to ensure smooth project execution Author, review, and approve regulatory documents and dossiers (e.g., QIMPD, NDA) ensuring compliance and data integrity Advanced degree (Master’s/PhD) in Chemistry, Pharmacy, or related field Solid experience in analytical development of synthetic drug substances Deep expertise in liquid chromatography (HPLC/UHPLC) and detection methods (MS, UV, fluorescence, CAD) Strong knowledge of analytical chemistry techniques (chromatography, titration, physicochemical methods) Proven leadership skills in project coordination, technical supervision, and mentoring Strong digital and analytical mindset, including data analysis and statistical evaluation Excellent communication skills in English with strong cross-functional collaboration abilities Opportunity to lead high-impact analytical development activities across clinical and commercial drug projects Exposure to cutting-edge analytical technologies within a global pharma R&D environment Strong potential for contract extension and growth within a world-class technical development organization Ihr Kontakt Referenznummer 879651/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
We maintain close relationships with customers across all industries and therefore can provide engineering specialists with exciting projects and attractive job opportunities, drawing on your personal interests and experience. As your professional companion, we support you throughout the entire process, from the first contact to the first day on your new job – all this completely free of charge.
We maintain close relationships with customers across all industries and therefore can provide engineering specialists with exciting projects and attractive job opportunities, drawing on your personal interests and experience. As your professional companion, we support you throughout the entire process, from the first contact to the first day on your new job – all this completely free of charge.
Register with us and reap the benefits of interesting job offers that match your skills and experience. Support the development and implementation of global and regional pricing guidance for pipeline and marketed products Conduct pricing analyses including external price benchmarking, international reference pricing and scenario modelling Monitor pricing and reimbursement trends in key markets and summarize potential risks and opportunities Assist in the preparation of pricing recommendations, business cases, and materials for internal governance forums Support launch pricing activities including early price guidance, forecasting, and alignment with regional teams Maintain pricing data accuracy across internal systems and dashboards in collaboration with global and local stakeholders Contribute to pricing tools, reports, and analytics to support decision making and long range planning Provide pricing support to affiliates and cross functional teams on standard pricing related questions and processes University degree in business, economics, finance, life sciences or a related field Initial experience in pricing, market access, finance, consulting, or analytics within healthcare or life sciences Good understanding of pharmaceutical pricing and reimbursement concepts, with interest in global pricing dynamics Strong analytical skills and ability to work with data, models, and financial assumptions Clear communication skills and ability to collaborate effectively in cross functional and international teams Strong attention to detail, structured thinking, and willingness to learn complex pricing systems and processes Proficiency in Excel and PowerPoint; experience with pricing or analytics tools is a plus A very renowned company Flat hierarchies Overtime compensation Ihr Kontakt Referenznummer 871577/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Register with us and reap the benefits of interesting job offers that match your skills and experience. Support the development and implementation of global and regional pricing guidance for pipeline and marketed productsConduct pricing analyses including external price benchmarking, international reference pricing and scenario modellingMonitor pricing and reimbursement trends in key markets and summarize potential risks and opportunitiesAssist in the preparation of pricing recommendations, business cases, and materials for internal governance forumsSupport launch pricing activities including early price guidance, forecasting, and alignment with regional teamsMaintain pricing data accuracy across internal systems and dashboards in collaboration with global and local stakeholdersContribute to pricing tools, reports, and analytics to support decision making and long range planningProvide pricing support to affiliates and cross functional teams on standard pricing related questions and processes University degree in business, economics, finance, life sciences or a related fieldInitial experience in pricing, market access, finance, consulting, or analytics within healthcare or life sciencesGood understanding of pharmaceutical pricing and reimbursement concepts, with interest in global pricing dynamicsStrong analytical skills and ability to work with data, models, and financial assumptionsClear communication skills and ability to collaborate effectively in cross functional and international teamsStrong attention to detail, structured thinking, and willingness to learn complex pricing systems and processesProficiency in Excel and PowerPoint; experience with pricing or analytics tools is a plus A very renowned companyFlat hierarchiesOvertime compensation Ihr Kontakt Referenznummer 871577/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Developing a phase-appropriate control strategy for drug substances and drug products Collaborating effectively with stakeholders across various departments Coordinating comprehensive analytical activities, which involves generating physical and chemical data for materials, developing/improving and validating analytical test methods or other analytical controls and ensuring thorough documentation, timely delivery and adherence to quality standards Coaching technicians and junior scientists on project work and serving as a central point of contact for project-related information Conduct work in compliance with cGMP where applicable, safety, and regulatory requirements Supervise internal laboratory activities and / or testing activities at CLOs/CDMOs Plan and document experiments/results independently and prepare for regulatory submissions such as IND and NDA A Master’s or Ph.D. in chemistry, pharmacy, or a related field, with at least three years of professional experience in analytical development of drug substances or drug products for small moleculesExpertise in key analytical techniques such as High-Performance Liquid Chromatography (HPLC), Ultra-Performance Liquid Chromatography (UPLC)Proven experience in developing and validating ICH-compliant analytical methodsProficiency in degradation and stability studies for small molecules, including forced degradation and impurity profilingUnderstanding of key requirements for drug substances and drug product specifications Excellent command of the English languageA strong quality mindset and excellent attention to detail. Digital savviness to support digital transformation initiatives; familiarity with statistical analysis of analytical data is also advantageousOpen-minded, goal-oriented, and able to work in a fast-developing environment.
Developing a phase-appropriate control strategy for drug substances and drug products Collaborating effectively with stakeholders across various departments Coordinating comprehensive analytical activities, which involves generating physical and chemical data for materials, developing/improving and validating analytical test methods or other analytical controls and ensuring thorough documentation, timely delivery and adherence to quality standards Coaching technicians and junior scientists on project work and serving as a central point of contact for project-related information Conduct work in compliance with cGMP where applicable, safety, and regulatory requirements Supervise internal laboratory activities and / or testing activities at CLOs/CDMOs Plan and document experiments/results independently and prepare for regulatory submissions such as IND and NDA A Master’s or Ph.D. in chemistry, pharmacy, or a related field, with at least three years of professional experience in analytical development of drug substances or drug products for small molecules Expertise in key analytical techniques such as High-Performance Liquid Chromatography (HPLC), Ultra-Performance Liquid Chromatography (UPLC) Proven experience in developing and validating ICH-compliant analytical methods Proficiency in degradation and stability studies for small molecules, including forced degradation and impurity profiling Understanding of key requirements for drug substances and drug product specifications Excellent command of the English language A strong quality mindset and excellent attention to detail. Digital savviness to support digital transformation initiatives; familiarity with statistical analysis of analytical data is also advantageous Open-minded, goal-oriented, and able to work in a fast-developing environment.