Job Description. Job Description. LGMPharma is a leading contract development and manufacturing organization (CDMO)and provider of Active Pharmaceutical Ingredients (API). With excellent APIsourcing and supply chain expertise together with our drug product. contractdevelopment. and manufacturing solutions, LGM is a premier end-to-end solutionsprovider to the global pharmaceutical industry. We are ahigh-growth organization looking to accelerate th...
We have an open position for a. Scientist, Analytical Sciences. for our Research and Development department located in the Irvine, CA facility. RESPONSIBILITIES. Extensive hands-on laboratory experience and background knowledge in materials and chemistry related to active pharmaceutical ingredients and excipients. Characterization of pharmaceutical materials with analytical techniques such as PAS, XRD, etc. on particle size distribution and cryst...
We have an open position for a. Quality Control Chemist B. in our Quality Department located in the Irvine, CA location. RESPONSIBILITIES. Perform and/or assist with analytical testing of raw materials, in-process samples, and finished products. Utilize analytical laboratory instrumentation, primarily the HPLC. Comply with cGMP regulations and follow all standard operating procedures. Peer review data generated by other technicians. Maintain and ...
Job Description. Job Description. LGMPharma is a leading contract development and manufacturing organization (CDMO)and provider of Active Pharmaceutical Ingredients (API). With excellent APIsourcing and supply chain expertise together with our drug product. contractdevelopment. and manufacturing solutions, LGM is a premier end-to-end solutionsprovider to the global pharmaceutical industry. We are ahigh-growth organization looking to accelerate th...
We currently have an open position for a Sr Quality Assurance Specialist reporting to our Quality Assurance department in the Irvine, location. RESPONSIBILITIES. Review all QC HPLC, GC, CE , AAS. TOC, UV, KF, FTIR and NIR assay and impurity results for Raw Materials, Finished Goods, Stability Products. Monitor all Controlled Products, Raw materials, Standards receiving, usage and inventory. Deacom Time editing for all QC analysts. Assisting Chem...