Lonza

Lonza in Slough is seeking a Scientist for the Analytical Development team. You will perform bioanalytical techniques, critically analyse data, and support method development while maintaining equipment and safety protocols. This is a fully on-site role, fostering real time collaboration and high technical precision in medicines manufacturing. The candidate should have a Life Sciences degree, hands-on lab experience, and a proactive, collaborative approach to problem solving.

United Kingdom, Slough Job Title: Scientist - Analytical Development team Location: Slough The Role We're seeking a motivated Scientist to join our fast-growing Analytical Development team. The successful candidate will be a key member of the laboratory team contributing to the delivery of bioanalytical development stages. You will be responsible for performing a variety of bioanalytical techniques, critically interpreting and analysing data and supporting optimisation and troubleshooting of methods. The role also includes involvement in equipment maintenance, document management and safety compliance. This is a fully site based role. Working together in person supports close, real time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What You Will Get An agile career and dynamic working culture An inclusive and ethical workplace Compensation programs that recognize high performance A variety of benefits dependant on role and location The full list of our global benefits can be also found on What You Will Do Working closely with study directors, execute experiments and critically analyse and interpret data to contribute to the establishment, pre-validation and development of bioanalytical methods such as SPR, flow cytometry, ELISA, cell-based methods. Draft internal and customer ready reports. Support effective lab and department operations including equipment ownership and maintenance, documentation, buffer preparation and safety actions. Support implementation of new assay technologies/continuous improvement projects. Contribute to technical investigations/RCAs. Maintain high-quality documentation in line with quality management systems. Train more junior members of the department as required. This role is fully on-site. What We Are Looking For Degree or Master's qualification in Life Sciences or a related scientific discipline. Laboratory experience in analytical or bioanalytical techniques required. Understanding of bioanalytical methods. Strong planning and organisation to deliver work on time. Effective communication and collaboration with peers and teams outside the department to provide customers with the highest service. Logical and organised approach to problem solving. A proactive mindset with a focus on innovation, efficiency, and continuous improvement. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Reference: R77640

United Kingdom, Slough Lab Informatics Lead Location: Slough Visa and relocation support is offered for the successful candidate. The Lab Informatics Lead will lead the development and continuous improvement of LIMS/ELN solutions supporting laboratory workflows, sample tracking, scientific data integrity. This role partners with laboratory teams, IT, and external vendors to deliver scalable, compliant, and user-friendly lab information management capabilities focusing on integrating laboratory equipment with a LIMS / ELN solution. This is a fully site based role. Working together in person supports close, real time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What You Will Get An agile career and dynamic working culture An inclusive and ethical workplace Compensation programs that recognize high performance A variety of benefits depending on role and location Explore our global benefits at . What You Will Do Define and maintain the product vision, roadmap, and backlog for LIMS/ELN integration Manage connections between LIMS/ELN, CDS, and instrument interfaces Gather requirements from scientists and lab managers, translating them into user stories Lead digitalization efforts to modernize lab environments Ensure workflows support sample management, reagent tracking, and data integrity Monitor system performance and identify opportunities for improvement What We Are Looking For Degree in Biotechnology, Biochemical Engineering, Biology, or related field Experience in product ownership or business analysis Hands on experience with ELN/LIMS platforms (e.g., IDBS, Benchling, ThermoFisher SampleManager, LabVantage) Knowledge of APIs and scientific instrument connectivity Familiarity with laboratory workflows in biopharma or biomanufacturing Understanding of data integrity, FAIR principles, and laboratory digitalization About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values-Collaboration, Accountability, Excellence, Passion, and Integrity-reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Reference: R67942

United Kingdom, Slough Senior Principal Scientist, Global Process Development Location: Slough, UK The actual location of this job is in Slough, UK. Join our Global Process Development team as a senior scientific expert, where you will lead strategic process development projects and help drive technical alignment across our global Biologics network. Using your expertise in biologic drug substance process development and manufacturing, you will solve complex technical challenges, influence scientific direction and enable the delivery of innovative solutions. This role is primarily based on site. Working together in person supports close, real time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. We offer flexibility to work remotely for no more than 20% of your time. Requests are considered on a case-by-case basis, in line with business needs. What You Will Get An agile career and dynamic working culture. The opportunity to work with senior scientific experts and multidisciplinary teams across a global Biologics network. Opportunities to lead high-impact, cross functional projects and influence global technical direction. An inclusive and ethical workplace. Compensation programs that recognize high performance. A variety of benefits dependent on role and location. The full list of our global benefits can be found here: . What You Will Do Lead multidisciplinary projects that implement technology changes and drive alignment across sites, ensuring delivery to agreed milestones, scope and quality standards. Lead matrix teams across functions and locations, building strong stakeholder relationships and securing alignment to achieve successful outcomes. Provide subject matter expertise across two or more relevant areas of upstream, downstream and/or bioconjugation process development and manufacturing for biologic drug substances. Troubleshoot complex technical challenges, using data analysis, multivariate approaches and root cause analysis to identify opportunities for process improvement and optimization. Monitor technical performance across the network and identify and address areas of technical misalignment. Present technical findings and recommendations to internal and external stakeholders, influencing decisions through clear scientific and technical communication. Coach and mentor scientists in Process Development, while contributing to the scientific and technical direction of the wider organization. What we are looking for: Extensive experience in bioprocessing, with a strong background in downstream processing and biologic drug substance process development and manufacturing. A proven track record of leading complex, multidisciplinary projects and matrix teams with minimal direction. Strong subject matter expertise in at least two relevant areas of bioprocess development and manufacturing. Experience using digital tools and advanced data analysis to understand and improve bioprocess performance. Experience with multivariate data analysis, process optimization and structured root cause analysis to solve complex technical challenges. Strong communication and stakeholder management skills, with the ability to influence technical decisions and communicate effectively with both technical and non-technical audiences. BSc, MSc, BEng or MEng in a relevant scientific or technical discipline; a PhD or equivalent is preferred. Business-fluent English is required. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Reference: R78836

QC Technologist (Method Validation) Duration: 12 Month FTC Location: Slough - This is a lab based role To contribute to scientific projects by generating and documenting laboratory data from experimental work. Progressively taking ownership of the laboratory environment as experience and seniority increases. This is a fully site based role. Working together in person supports close, real time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What you will get An agile career and dynamic working culture An inclusive and ethical workplace Compensation programs that recognize high performance A variety of benefits dependent on role and location Explore our full list of global benefits: What you will do Conduct laboratory experiments and analytical testing in accordance with established procedures, with appropriate guidance and support. Plan, organise, and deliver assigned project activities to ensure work is completed accurately and within agreed timelines. Analyse, interpret, and accurately record experimental data, contributing to technical reports, data tables, and project documentation. Support troubleshooting activities and participate in out-of-specification (OOS) and laboratory investigations to help resolve technical challenges. Maintain laboratory equipment and workspaces, including routine instrument maintenance, housekeeping activities, and monitoring reagent and consumable inventory levels. Ensure compliance with company policies, quality standards, regulatory requirements, and Good Laboratory Practice (GLP/GMP) guidelines where applicable. Collaborate effectively with colleagues and cross functional teams to support the successful delivery of scientific and operational objectives. What we are looking for Degree in a scientific or quality related discipline Basic knowledge of Analytical Laboratory methods for use in protein analytics Outstanding organizational skills to manage tasks efficiently and meet deadlines Strong problem solving abilities to address and resolve challenges promptly About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Lonza in Slough is seeking a detail-oriented QC professional to join the Raw Materials team. You will perform testing of raw material samples and document results in compliance with GMP, contributing to timely batch release. The role requires experience in QC laboratories and a strong understanding of GMP systems. You will collaborate across teams, mentor junior staff, and drive continuous improvement to quality and efficiency in a fast-paced manufacturing environment.

We are seeking a motivated and detail-oriented professional to join our QC Raw Materials team. In this role, you will be responsible for delivering high-quality analytical and operational support while ensuring activities are completed within agreed timelines and in accordance with GMP requirements. Working with general guidance from senior team members, you will demonstrate a strong commitment to quality, continuous improvement, and operational excellence within a fast-paced custom manufacturing environment. As a key member of the team, you will be expected to execute work accurately and efficiently, adapt to changing priorities, and contribute to maintaining the highest standards of compliance and quality. You will also play an important role in supporting and mentoring junior colleagues, helping to foster a collaborative culture and ensure consistent performance across the department. This is a fully site based role. Working together in person supports close, real time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What you will get: An agile career and dynamic working culture An inclusive and ethical workplace Compensation programs that recognize high performance A variety of benefits dependant on role and location Perform testing of raw material samples and accurately document results in accordance with GMP requirements, approved procedures, and established timelines. Critically evaluate analytical data, identify potential issues or trends, and escalate findings to QC Management as appropriate. Review and approve data, records, and results generated by other team members, ensuring accuracy, compliance, and data integrity. Lead and support quality system activities, including the investigation and completion of Deviations, Change Controls, OOS/OOT investigations, CAPAs, and other GMP quality records. Drive continuous improvement initiatives to enhance GMP compliance, laboratory efficiency, safety, and overall quality performance. Effectively manage changing priorities, proactively communicate risks to timelines, and escalate delays or operational challenges when required. Support raw material disposition activities and collaborate with cross-functional stakeholders to ensure timely decision making. Provide guidance and mentorship to junior team members, promoting best practices and ensuring consistently high standards of work within the QC function. Champion a culture of quality, compliance, and continuous improvement, ensuring all activities are performed in accordance with GMP standards and company procedures. What we are looking for: Degree or Master's qualification in Life Sciences or a related scientific discipline. Experience working within a QC laboratory and/or GMP manufacturing environment. Previous involvement in investigations, deviations, CAPAs, and continuous improvement initiatives. Proven experience in chemical and/or biochemical testing techniques, with the ability to generate, interpret, and report analytical data accurately and effectively. Strong understanding of GMP principles and quality systems, with a track record of maintaining compliance, completing quality documentation, and adhering to regulatory requirements. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Lonza, based in the United Kingdom (Slough), seeks a Lead Scientist to drive potency ELISA and cell-based analytics. The role emphasizes bench leadership, problem solving, and delivering high-quality, data-driven solutions in a fully site-based setting. You will mentor junior scientists, introduce new technologies, and shape project directions in a fast-paced environment. The ideal candidate has strong expertise in potency ELISA, cell-based assays, and SPR/Biacore, with proven project leadership

Lead Scientist - Potency, ELISA & Cell-Based Analytics United Kingdom, Slough Job Title: Lead Scientist - Potency ELISA & Cell-Based Analytics Location: Slough The role: We're looking for a scientifically curious and technically expert Lead Scientist to join our Analytical Development team. This is a pivotal role for someone who thrives on solving complex problems, leading from the bench, and working to deliver high-quality, data-driven solutions. If you bring strong expertise in potency ELISA, cell-based assays, and/or SPR/Biacore, this is your opportunity to make a real impact in a collaborative, fast-paced environment. This is a fully site based role. Working together in person supports close, real time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What you will get: An agile career and dynamic working culture An inclusive and ethical workplace Compensation programs that recognize high performance A variety of benefits dependant on role and location Lead and deliver multiple complex analytical projects, ensuring high-quality outcomes right first time - this will include method development, establishment and (pre validation activities) Lead the implementation of new technology and customer specific methods Act as a technical expert in potency ELISA and cell-based methods and/or SPR/Biacore Design, plan and execute complex experimental strategies, translating customer needs into practical solutions Analyse and interpret data to generate robust scientific insights and process understanding Present data, troubleshoot issues, and shape project direction Mentor and coach junior scientists, building capability across the team Drive innovation and continuous improvement Lead investigations, identify risks early, and ensure timely, effective resolution What we are looking for: Degree or Master's qualification in Life Sciences or a related scientific discipline. Strong laboratory experience in analytical or bioanalytical development Proven expertise in potency ELISA and cell-based assays, including method development and troubleshooting and/or strong experience with Biacore/SPR techniques and data interpretation Proven ability to lead complex projects and influence outcomes across multiple teams and sites Confident communicator, able to translate complex data into clear, actionable insights Passion for mentoring, collaboration, and driving scientific excellence About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Lonza in Slough is seeking an R&D Lead Scientist to design and execute purification process development studies using high-throughput workflows. You will translate project objectives into clear study plans and deliverables while maintaining data integrity and safety. You will work closely with analytical, automation, bioinformatics and data science colleagues to advance technology implementation and provide scientific leadership across projects.

R&D Lead Scientist Slough, UK Join Lonza's Research & Development team in Slough and help shape the next generation of bioprocessing technologies. As an R&D Lead Scientist, you will design and execute innovative purification process studies, using high-throughput workflows and data-driven approaches to develop robust solutions for the biopharmaceutical industry. This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to develop and manufacture medicines to the highest quality and safety standards. What you will get: An agile career and dynamic working culture. The opportunity to contribute to innovative bioprocess development within a global life sciences organisation. An inclusive and ethical workplace where collaboration and new ideas are valued. Compensation programs that recognise high performance. A variety of benefits dependent on role and location. The full list of our global benefits can be found here: What you will do: Design, plan and independently execute purification process development studies, translating project objectives and scientific questions into clear study plans and deliverables. Develop, optimise and implement high-throughput workflows to accelerate process development, improve efficiency and support scalable development pipelines. Configure and operate high-throughput equipment, ensuring robust monitoring, data capture and effective troubleshooting. Analyse experimental data, draw scientifically sound conclusions and provide clear recommendations to guide process development decisions. Identify potential risks to study delivery and implement appropriate mitigation strategies while maintaining high standards of quality, data integrity and safety. Work collaboratively with analytical, automation, bioinformatics and data science colleagues, as well as purification development teams, to advance technology implementation. Provide scientific and technical leadership within projects, sharing knowledge and contributing to continuous improvement and a culture of innovation. What we are looking for: A strong scientific or engineering background in biotechnology, chemistry, chemical engineering or a related discipline, supported by a BSc/BEng or equivalent experience; postgraduate qualifications such as an MSc/MEng or PhD/EngD are advantageous. Advanced laboratory experience, with the ability to independently plan and execute complex experimental studies and translate scientific principles into practical applications. Experience developing, optimising or applying high-throughput workflows, laboratory automation or related bioprocessing technologies is highly desirable. Strong data analysis and scientific problem-solving skills, with the ability to interpret experimental results and communicate clear conclusions and recommendations. Excellent technical writing and presentation skills, with experience preparing high-quality reports and communicating scientific ideas effectively to different stakeholders. A collaborative and proactive approach, with the ability to build effective relationships across multidisciplinary teams and take ownership of deliverables. A strong commitment to quality, data integrity, laboratory safety and good laboratory practices, with an interest in the application of bioprocessing technologies within a regulated environment. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Lonza Cambridge is seeking a Lead Scientist in Cell Expression Technologies to drive R&D on CHO-based expression platforms, including advances in molecular biology and factory-scale transfer of new technologies. You will lead projects, mentor junior scientists, and spend approximately 80% of your time hands-on in the laboratory, delivering expression solutions for complex therapeutic proteins with high quality standards.

Lonza in Slough is seeking a Scientist for QC Product Testing & Stability to perform analytical testing of therapeutic protein samples in a GMP environment. You will apply HPLC, capillary electrophoresis, spectrophotometry and other methods, review data against specifications and contribute to stability studies and quality investigations. The role is site-based, requiring close collaboration with Quality Control, Quality Assurance and Manufacturing to ensure medicines meet the highest standards

Scientist - QC Product Testing & Stability Slough, United Kingdom Join Lonza's QC Product Testing & Stability team in Slough and play a key role in ensuring the quality and stability of therapeutic protein products that help improve patients' lives. This is an exciting opportunity for a laboratory-based scientist to apply analytical expertise in a regulated GMP environment while developing technical and quality assurance experience. This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What you will get An agile career with opportunities for technical and professional development. A collaborative, inclusive and ethical working environment. Competitive compensation and recognition for high performance. A comprehensive range of benefits relevant to your role and location. Opportunities to contribute to continuous improvement projects and develop mentoring experience. Perform analytical testing on therapeutic protein samples using techniques including HPLC, capillary electrophoresis, spectrophotometry and other physicochemical methods in accordance with GMP requirements, SOPs and study protocols. Review analytical data for technical accuracy, interpret results against specifications, identify trends and communicate observations to key stakeholders including Study Directors, Quality Assurance and Manufacturing. Prepare stability study protocols, testing summaries and technical reports to support product quality and stability programmes. Support investigations, deviations, CAPAs and change controls, independently leading routine quality investigations where appropriate. Mentor and support colleagues by sharing technical knowledge, providing training and promoting best laboratory practices. Contribute to laboratory operations through equipment monitoring, reagent and consumable management, housekeeping and continuous improvement initiatives. Work collaboratively across Quality Control, Quality Assurance and Manufacturing to ensure customer, regulatory and business requirements are consistently met. What we are looking for Degree in Chemistry, Biochemistry or another relevant scientific discipline, or equivalent relevant laboratory experience. Experience working within a GMP-regulated pharmaceutical or biological laboratory environment. Practical knowledge of analytical techniques such as HPLC, capillary electrophoresis, spectrophotometry or other protein characterisation methods. Understanding of cGMP principles and their application within a quality-controlled laboratory. Strong analytical and problem-solving skills with the ability to interpret data and identify trends. Excellent organisational and communication skills with the ability to prioritise work and collaborate effectively within a multidisciplinary team. A proactive mindset with a commitment to continuous learning, quality, safety and process improvement. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Lonza Slough site is seeking a Site Finance Business Partner to enable short- and long-term targets by delivering insightful financial analysis. The role covers cost transparency, product profitability, and key KPIs within production, innovation, and working capital. It requires hands-on operation, strong costing knowledge, and effective stakeholder influence in a hybrid 4-on-site/1-on-site- policy. You will manage monthly closes, outlooks, risks and opportunities with Platform Controlling,

Site Finance Business Partner Location: Slough, United Kingdom Hybrid Working Policy - 4 days on Site, 1 day WFH. The Site Finance Business Partner is a key member of the Slough Finance team. The role is responsible for enabling the Departments to reach short-and long-term targets by providing insightful analysis and recommendations in all financials aspects of the Site such as (but not limited to) cost transparency, Inventory, product profitability, key performance indicators in production, innovation, cost savings, planning cycles and net working capital. What you will get An agile career and dynamic working culture An inclusive and ethical workplace A variety of benefits tailored to your localality. Enabling the Site to reach short-and long-term targets by providing insightful analysis and recommendations in all financials aspects of the plant such as (but not limited to) cost transparency, product profitability, key performance indicators in production, innovation, cost savings, planning cycles and net working capital Managing monthly financial closing, Outlooks and Risks and Opportunities process together with Platform Controlling (Revenue to Gross Profit; balance sheet and NWC) Deliver high quality, robust, and well governed financials in support of the Business Strategy Review and Target processes. Ensure financial plans, assumptions, and outputs are accurate, consistent, clearly articulated and timely aligned with Site Leadership Investment Support for various CAPEX projects Leading process and systems improvement projects (SAP enhancements, new process and tools introductions etc.) together with local and global supply chain group, corporate accounting and global operations What we are looking for Strong business partnering skillset with an ability to influence others Professionally qualified accountant (ACCA or CIMA). Previous experience in a manufacturing finance environment is highly desirable. Hands on approach with a willingness to be actively involved in day to day operational activities. Strong knowledge and practical experience of standard costing and operational variance analysis is essential. Excellent communication and stakeholder management skills, with the confidence to influence and challenge senior business leaders. Experience supporting or leading ERP system implementations would be advantageous. Commercially minded with a proactive, problem solving approach and a focus on driving operational and financial performance. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Lonza in Slough is seeking a Senior Director, Head of Supply Chain, responsible for overseeing the end-to-end supply chain performance, ensuring reliable execution of customer programs while optimizing capacity and costs. This leadership role involves integrating customer demand into supply strategies aligned with Lonza's global network, driving excellence in planning processes and supply chain transformation. Ideal candidates possess strong experience in managing operations within regulated environments and have demonstrated leadership skills in complex settings.

The Senior Director , Head of Supply Chain for Slough is accountable for the end to end supply chain performance of the manufacturing site, ensuring reliable execution and delivery of customer programs while optimizing capacity, inventory, and cost. As a member of the Site Leadership Team, this role translates customer demand and portfolio priorities into integrated, executable supply strategies aligned with Lonza's global supply chain network. The role plays a critical part in driving planning excellence, S&OP governance, and supply chain transformation to support growth, operational excellence, and customer commitments in a highly regulated manufacturing environment. Key Responsibilities Own and lead end to end site supply chain performance, from demand planning through execution, logistics , and customer delivery. Lead the integrated site planning process, translating customer demand and portfolio priorities into executable plans across assets, materials, and workforce. Govern the site S&OP process, providing scenario analysis and recommendations on demand prioritization, capacity allocation, and financial impact. Ensure reliable supply chain execution, including planning, materials management, warehouse, and logistics operations. Optimize inventory levels, capacity utilization , and cost performance while maintaining full compliance with quality, safety, and regulatory requirements. Drive supply chain transformation initiatives, including digital planning capabilities, SAP, and advanced planning tools, to improve visibility, forecast accuracy, and performance. Develop, lead, and retain a high performing supply chain organization, ensuring strong capabilities, succession planning, and talent development. Partner closely with global supply chain, commercial, and network planning teams to integrate customer programs and support long term network strategy. Contribute to cross site, regional, or network initiatives, operational excellence programs, and special projects as required. Key Requirements Bachelor's degree in Supply Chain , Business, or a related field; MBA or advanced degree preferred. Extensive senior level experience in supply chain leadership roles within manufacturing environments. Strong experience in regulated industries such as biotech, pharmaceutical, CDMO, or chemicals. Proven track record leading site level supply chain operations and S&OP processes. Solid experience with SAP and digital planning tools across materials, scheduling, and capacity planning. Demonstrated leadership capability within complex, matrix, and multi stakeholder environments. Ability to drive transformation, change, and continuous improvement at scale. Excellent communication, influence, and stakeholder management skills. Customer focused mindset with strong business acumen and data driven decision making. At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

You will be based at our Visp site, supporting global warehouse and supply chain operations through SAP EWM solutions in a regulated GMP/ GxP environment. This role offers the opportunity to make a tangible impact on critical systems that enable reliable and compliant manufacturing. The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. What you will get: An agile career and a dynamic work culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below. Benefits in Visp: assetstream.aspx () What you will do: Design, build, and enhance SAP EWM solutions supporting warehouse and labeling operations Act as an IT business partner, translating business needs into functional specifications Lead or contribute to initiatives as a functional lead Configure and customize SAP EWM in line with global processes and governance Support testing, validation, and audit readiness in a GMP/ GxP environment Provide third level support for complex system incidents and problems Drive continuous improvement by identifying optimization and innovation opportunities What we are looking for: Proven experience with SAP EWM and solid knowledge of SAP WM and SAP MM Experience working with SAP S/4HANA EWM, embedded or decentralized Experience working with complex automated warehouse environments; exposure to AGV-integrated landscapes, robotics, or warehouse control systems (WCS/MFS) is an advantage Understanding of warehouse automation and system integration concepts Previous experience in pharmaceutical or CDMO industries is preferred Strong analytical skills with a structured approach to problem solving Ability to collaborate and communicate effectively with stakeholders in English, German fluency is highly desired. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

You will be based at our Visp site, supporting global warehouse and supply chain operations through SAP EWM solutions in a regulated GMP/ GxP environment. This role offers the opportunity to make a tangible impact on critical systems that enable reliable and compliant manufacturing. The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. What you will get: An agile career and a dynamic work culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below. Benefits in Visp: assetstream.aspx () What you will do: Design, build, and enhance SAP EWM solutions supporting warehouse and labeling operations Act as an IT business partner, translating business needs into functional specifications Lead or contribute to initiatives as a functional lead Configure and customize SAP EWM in line with global processes and governance Support testing, validation, and audit readiness in a GMP/ GxP environment Provide third level support for complex system incidents and problems Drive continuous improvement by identifying optimization and innovation opportunities What we are looking for: Proven experience with SAP EWM and solid knowledge of SAP WM and SAP MM Experience working with SAP S/4HANA EWM, embedded or decentralized Experience working with complex automated warehouse environments; exposure to AGV-integrated landscapes, robotics, or warehouse control systems (WCS/MFS) is an advantage Understanding of warehouse automation and system integration concepts Previous experience in pharmaceutical or CDMO industries is preferred Strong analytical skills with a structured approach to problem solving Ability to collaborate and communicate effectively with stakeholders in English, German fluency is highly desired. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.