At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success. Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia.
We strive to be the leading supplier using science and technology to improve the quality of life.
We work with passion, using advanced technologies, to transform life science into new possibilities for our customers.
Do you want to help us as we shape the future of this great organization?
Job Description Summary
Writes Assay Qualification Protocols and Reports according to Lonza standards and SOPs.
Writes Assay Validation Protocols and Reports according to Lonza standards and SOPs.
Responsible for performing Assay Development and Optimization and evaluating methods received from client for equipment and materials gaps prior to starting transfer activities.
May perform assays in support of Development process work.
Writes Method SOPs and Forms. Reports test results, maintains raw data, and accurate laboratory records in accordance with applicable SOPs.
Interacts with clients in Joint Project Team meetings regarding method development, optimization, qualification, validation and technical challenges.
Trains QC Analysts on new methods during Assay Tech Transfer activities. Also interacts with QC on equipment platform alignment and assay qualification/validation strategies.
Serve as SME on specific assays. May serve in consultation role on difficult Laboratory Investigations in QC as needed.
Performs other duties as assigned.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.