Miltenyi Biotec Benefits Overview

Manufactures biologics and lentiviral vectors under cGMP conditions in a cleanroom laboratory. Executes batch records, follows aseptic gowning and SOPs, maintains equipment, cleans work areas, manages supplies, and supports calibration and validation. Drafts and reviews GMP documentation, including change controls, investigations, deviations, and manufacturing procedures. Troubleshoots processing issues, supports root-cause analysis and corrective actions, follows production schedules, and trains new staff.

Develop and optimize spatial biology, multiomics sequencing, and in situ sequencing workflows for commercial platforms. Design and analyze experiments, prepare samples and libraries, run sequencing assays, validate performance, develop reagent panels, troubleshoot technical issues, and support technology transfer and commercialization. Collaborate with scientists, engineers, and product teams; document procedures, maintain laboratory operations, present findings, and mentor junior staff while following safety and regulatory requirements.

Leads analytical method transfers for cellular therapy products into Process Sciences, serving as a liaison between Process Sciences and Quality Control. Supports stability programs, R&D, GMP documentation, protocols, reports, investigations, CAPA, risk assessments, and continuous improvement projects. Mentors junior staff and troubleshoots analytical issues. Requires expertise in immunoassays, flow cytometry, ELISA, qPCR, advanced analytical methods, cGMP regulations, validation, qualification, transfer, and statistical analysis. Travel is 10–20% domestically and internationally.