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Kindeva Drug Delivery is seeking a Senior QC Chemist to join our Northridge site. This individual will perform complex analytical testing on incoming raw materials and finished pharmaceutical products in a GMP-regulated environment. The role also supports laboratory investigations, documentation, and continuous improvement initiatives. This is a fast-paced manufacturing environment requiring strong technical expertise, adaptability, and attention to detail.
Job Responsibility:
Perform analytical testing using HPLC, GC, FTIR, UV, dissolution, and other lab instrumentation
Test raw materials and finished products per USP/compendial methods and internal specifications
Prepare solutions, standards, and reagents
Lead or support laboratory investigations, deviations, and CAPA
Author and review SOPs, methods, and lab documentation
Support equipment qualification, calibration, and maintenance
Drive safety and continuous improvement initiatives
Requirements:
Bachelor's degree in Chemistry or related science
Pharmaceutical industry experience in a GMP/GXP environment
Strong knowledge of GMP/GLP requirements
Approximately 10 years of analytical testing experience
Advanced HPLC expertise
Experience leading lab investigations
U.S. Citizen or Green Card Holder
Local candidates only (no relocation)
Must pass drug and background screening
Nice to have:
Experience with inhalation or transdermal products
Strong understanding of global compendia and ICH guidelines