BioLegend has an immediate opening for a Quality Assurance Lead to oversee all applicable Quality Assurance processes for our US FDA registered cGMP manufacturing facility. This position will take the lead in ensuring the successful implementation of our MDSAP program. This is an opportunity with exciting career advancement opportunities that will spearhead the alignment of our existing quality system and applicable regulations with BioLegend’s Regulated product development activities.
This position will be responsible for supporting key quality elements such as document control, investigation management, validation, training, nonconformance, complaint management, and CAPA systems. The Quality Assurance lead will also be responsible for reviewing the quality records and final product releases per established quality management system.
Join us in enabling legendary discovery!
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Minimum Qualifications - Education and Experience
Preferred Qualifications – Education and Experience