Conduct hands-on lab work in protein purification and process development, ensuring quality standards under cGMP regulations, leading projects, and drafting documentation.

The QA Expert will oversee daily Quality Assurance activities, ensuring compliance with SOPs in a cGxP manufacturing environment. Responsibilities include reviewing SOPs, participating in audits, coordinating Quality systems, and leading process improvements in quality assurance.

The trainee will support the Development Services department, working on processes for the manufacture of protein therapeutics. Responsibilities include cell culture development, purification process support, conducting analytical tests, lab maintenance, and following EHS regulations under supervision. Fresh graduates and those without industry experience are encouraged to apply.

Join the Characterization team focusing on protein characterization using mass spectrometry and analytical methods. Responsibilities include executing analytical tests, analyzing data, ensuring compliance with GMP guidelines, reviewing documentation, and contributing to laboratory support. Ideal candidates have a relevant science degree, strong problem-solving skills, and can work effectively in a team.

As a Biotechnologist Trainee, you will be responsible for manufacturing therapeutic proteins in a GMP environment, performing laboratory tasks, equipment monitoring, and maintaining facility standards. You will learn procedures, demonstrate aseptic techniques, and contribute to manufacturing operations under supervision.

The Technologist 2 will support laboratory operations, ensuring compliance with EHS rules and good laboratory practices. Responsibilities include daily equipment maintenance, preparation of media and reagents, stock management, and contributing to operational efficiency while adhering to GMP requirements.

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.

The CCP5 Trainee is responsible for the manufacturing of therapeutic proteins in a GMP environment, involving equipment handling, routine tasks in clean rooms, and maintaining compliance with cGMP practices. The role requires learning procedures, basic troubleshooting, and teamwork to support manufacturing operations, with daily supervision and opportunities for training.

The QA Trainee will support Quality Assurance activities in a cGxP contract manufacturing facility, manage GMP documents, analyze data, and provide compliance support while demonstrating teamwork and problem-solving skills.

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.

The Logistics Assistant is responsible for supporting daily operations regarding receipt, storage, and shipment of materials. The role requires understanding of logistics functions and SAP transactions, maintaining inventory accuracy, responding to inquiries, and ensuring compliance with quality systems and safety protocols, while working with minimal supervision and willingness to learn.

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 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.

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 Biotechnologist is responsible for manufacturing cell therapy products in adherence to cGMP regulations. Key duties include executing batch records, performing environmental monitoring, maintaining compliance training, and troubleshooting technical issues. The role demands flexibility with a rotating 12-hour shift schedule and operating in a cleanroom environment.

As a QC Analyst at Lonza, you will conduct tests and analyze products and samples following SOPs and cGMP. Responsibilities include documentation review, equipment troubleshooting, and participation in investigations. You'll support quality control initiatives and contribute to continuous improvements within the laboratory setting.

The Process Data Expert will utilize advanced data science techniques to develop analytical tools, solve bioprocessing problems, and improve data utilization at Lonza.

The Senior Specialist, Operational Excellence is responsible for driving process improvement and supporting Lean Six Sigma projects. Key responsibilities include leading continuous improvement projects, coaching team members, managing stakeholders, facilitating training, and using various operational excellence tools to enhance business performance.

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.