As a trainee in Development Services at Lonza, responsibilities include developing cell lines, purification processes, and conducting analytical testing. The role requires adherence to EHS rules, lab support tasks, and compliance with Good Manufacturing Practices. Fresh graduates with relevant science degrees are welcome to apply.

The role involves executing and analyzing tests related to protein characterization using various analytical techniques, ensuring compliance with regulatory guidelines, collaborating with teams, and contributing to lab support and safety training.

The Deviation Investigation Intern at Lonza will support daily tasks in a cGMP manufacturing facility, engaging in technical investigations and writing deviation reports. Responsibilities include maintaining deviation trackers, conducting root cause analyses, collaborating with SMEs, and supporting continuous improvement initiatives. This role provides hands-on experience in the biopharmaceutical industry.

The CCP5 Trainee will be responsible for the manufacture of therapeutic proteins under cGMP conditions, performing laboratory tasks and equipment monitoring, while working in clean room environments. They will learn procedures, attend ongoing training, and support manufacturing operations while maintaining high facility standards and adhering to schedules.

As a Technical Writing & Planning Intern at Lonza, you will support the Technical Writing Team and Planning team, focusing on developing and revising Master Batch Records, managing documents, and collaborating with stakeholders. The role involves gaining insights into cGMP, bioprocessing, and participating in continuous improvement projects.

The QA Manager is responsible for overseeing the Aseptic Processing Program and Environmental Monitoring within the Cell and Gene Therapy entity, ensuring compliance with US and international standards. This role requires expertise in sterility assurance, microbial control, and cleanroom management, along with reviewing policies, documentation, and supporting regulatory audits and investigations.

The Analytical Scientist will execute analytical studies in compliance with ICH guidelines and GMP principles. Responsibilities include conducting analytical testing, interpreting data, managing multiple projects, and reviewing GMP documentation. The role requires strong communication skills and the ability to lead problem-solving efforts. The candidate will become a Subject Matter Expert in their area and contribute to departmental improvement projects.

As a Senior Specialist QC at Lonza, you will supervise laboratory data review, author and review necessary documentation, interact with customers and regulatory agencies, troubleshoot analytical and microbiological methods, and lead method validations and transfers. Additionally, you will coach junior team members and participate in audits.

Assist Operational Buyer with daily tasks including reviewing orders in SAP, data entry, and supplier assessments. Conduct presentations of status updates and collaborate with teams to optimize supply chain processes. Gain exposure to compliance, cGMPs, and various data management systems.

As a QC Expert, you will supervise testing techniques and coordinate with departments for timely test results, review laboratory data, author regulatory documents, lead projects aimed at quality improvements, and coach junior team members. You will leverage your extensive QC experience to ensure compliance and resolve analytical challenges.

As a QA Specialist, you will oversee QA activities in a GMP biotech contract manufacturing facility, reviewing documents, managing compliance with regulatory standards, troubleshooting issues, and leading small projects. Your role also includes developing training and ensuring operational quality and safety.

The Analyst 1, QC is responsible for conducting various testing/analysis to support business needs, documenting results following cGMP, troubleshooting analytical methods, and assisting in equipment qualification and lab maintenance.

The Associate Department Manager, Systems QC will lead the Quality Control team, overseeing material and product testing, ensuring regulatory compliance, and fostering a high-performing team environment. Responsibilities include managing computerized QC systems, maintaining LIMS, troubleshooting system issues, developing personnel, and establishing QC policies.

The Logistics Assistant will manage daily operations, ensuring efficient workflow in shipping, receiving, and warehouse functions. Key responsibilities include handling SAP transactions, maintaining inventory accuracy, investigating logistics inquiries, and monitoring compliance. The role requires knowledge of logistics workflows, material safety, and quality systems, alongside flexibility for cross-training and supporting various warehouse tasks.

The Engineer 2, Control Systems at Lonza is responsible for the implementation and support of computerized systems in GMP manufacturing of biologics products. Key responsibilities include system maintenance, user access management, issue resolution, and ensuring compliance with regulatory requirements. The role involves collaborative support with multifunctional teams and oversight of control system policies.

As an EHS Specialist, you will support the EHS department by conducting routine inspections, managing EHS records and training, ensuring compliance with regulations, overseeing safety equipment, and assisting with waste management. You will help maintain the EHS management system and perform various administrative tasks related to EHS activities.

As a Senior Principal Scientist, you will lead multi-disciplinary projects in process development, focusing on upstream and downstream processes for biologic drug substances. You will act as a Subject Matter Expert, guide matrix teams, manage project milestones, and utilize digital tools for data analysis, all while mentoring junior scientists. Your goal is to improve process efficiency and ensure alignment across Lonza's global network.

The Process Analytics Scientist will perform analytical testing on therapeutic products, utilize high-throughput assay platforms, troubleshoot, optimize methods, and lead scientific projects. Key responsibilities include preparing protocols, ensuring compliance with regulations, and providing training to junior scientists.

The Biotechnologist will manufacture cell therapy products and media at Lonza, following cGMP regulations. Responsibilities include executing batch records, maintaining training status for GMP tasks, performing environmental monitoring, and equipment cleaning. The role requires a deep understanding of compliance, troubleshooting, and participation in continuous improvement initiatives, all while working in a clean room environment with a rotating shift schedule.

The Senior Process Engineer for MSAT (USP) will oversee the transfer of cell culture or purification stages from customers' processes to Lonza's operations, engage in technical investigations, assist with plant startup, and provide training for manufacturing operators. This role requires collaboration across departments and with customers to ensure compliance and robustness of manufacturing processes.