Lonza Jobs in United States

The Manufacturing Operator is responsible for providing support functions to the manufacturing process. · ...

The Quality Control (QC) Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. · Running test samples for in-process, lot release and stability studies. · Reviewing assays. · Writing qual ...

Join Lonza in Vacaville, CA, as a Master Manufacturing Technician – Bioprocess and be part of a hard-working team dedicated to producing innovative bio-therapeutic medicines. · ...

This role provides hands-on exposure to Good Manufacturing Practices (GMP), quality systems, documentation control, investigations and compliance activities. · ...

This position is responsible for the order changes on hard capsule machines (HCMs) and various other equipment such as Unified, Unisor, ILD, iBox etc as well as assisting to get equipment back into production. · ...

Job summary · At Lonza AG, we are committed to crafting a healthier world by offering innovative solutions that consistently surpass expectations. We are looking for a dedicated and dynamic individual to join our team as a Pharmaceutical Warehouse Operator.This is an outstanding ...

We are seeking a motivated and detail-oriented intern to join our Product Development team. You will assist in the design and testing of drug products for oral and pulmonary delivery. · Apply knowledge of chemistry and material science fundamentals to assigned problem statements. ...

The QC Associate I is responsible for the performance of direct materials testing in accordance with cGMP regulations. · Perform testing of routine and non-routine samples and documents according to GMP · Review data and assess against established acceptance criteria, identify di ...

Join Lonza AG as a Global Controls Engineer – Automation and help shape the future of life sciences through cutting-edge automation solutions. · Develop, replicate, and support global automation systems across sites in Belgium, France, US, Mexico, China, Japan, and India. · ...

This Logistics Specialist II role involves taking samples of incoming raw materials and performing routine testing in compliance with Good Manufacturing Practice (cGMP) and standard operating procedures (SOPs) · An agile career and dynamic working culture. · An inclusive and ethi ...

Join Lonza AG as a Diagnostics Technician in Greenwood, SC, USA. This position is responsible for the operation of hard capsule machines (HCM) that produce capsules for Lonza Greenwood. · ...

Serves as the commercial ops and strategic partner to the AMER RBU Lead driving execution of commercial strategy value drivers and programs across the region. · The role ensures consistent application of global standards enables cross-functional alignment and reinforces commercia ...

The Commissioning, Qualification and Validation (CQV) Engineer IV supports the commissioning and qualification of equipment and systems.This role performs validation activities to include but not limited to equipment set up, managing protocols, maintenance (PRVM) and reviewing do ...

We are looking for a Senior Manager, Ethics & Compliance Investigator to lead internal investigations across a wide range of issues. · ...

The MSAT Scientist III is responsible for being the primary technical support lead during process support lead for manufacturing processes. · Bachelor of Science degree required in Biotechnology area, Biological Sciences or Chemical Engineering. · A minimum of five years experien ...

This job leads the QC department, overseeing biochemistry, microbiology and environmental monitoring. It will develop and execute QC strategy aligned with site goals ensuring compliance with cGMP and safety regulations. ...

Join Lonza as a QA Specialist III – Raw Materials Compliance to provide operational support and ensure compliance throughout the raw material lifecycle. · ...

The Quality Control (QC) Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. · Running test samples for in-process, lot release and stability studies. · Reviewing assays. · ...

As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes. · An agile career and dynamic working culture · An inclusive and ethical workplace · Compensation programs that recognize high performance i ...

We have an open position for a paid internship as a Mechanical Engineer Intern with our Engineering team at our location in Bend, OR. · Support the mechanical engineering team helping with the design installation repair and modification of pharmaceutical processing equipment. · ...