The Sr. Specialist, Quality Control is tasked with conducting regular product evaluations, visual assessments, and microbiological tasks for both clinical and commercial products. This position encompasses the management of laboratory samples, aiding in audits, and upholding compliance with current Good Manufacturing Practice (cGMP) regulations. Applicants should have a Bachelor’s degree in a science-related field and a minimum of 5 years of experience within a cGMP-regulated quality control or analytical setting. Key attributes for success in this role include excellent organizational abilities, meticulous attention to detail, and the capacity to work autonomously.
CELULARITY LLC provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
