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Join a pioneering organization in regenerative medicine as a Quality Control Analyst I, where you will play a crucial role in ensuring the quality of groundbreaking therapies. This position involves performing routine testing and analysis of raw materials and drug products, contributing to the development of innovative treatments that transform patient care. You'll work in a collaborative environment, gaining valuable experience in a cGMP laboratory setting while supporting a mission-driven team dedicated to improving lives. If you are passionate about science and quality assurance, this opportunity is perfect for you.
Job Description
At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking treatments including MACI (knee cartilage repair), Epicel and Nexobrid (burn care).
Position Summary:
The Quality Control Analyst I is responsible for performing routine testing of raw materials, in-process, drug product (DP) and stability samples within the QC laboratory in accordance with SOPs for product release and validation.
Schedule: As a company that thrives on teamwork and collaboration, this role will be required to work on-site 5 days per week: Tuesday-Saturday.
Position Scope:
Qualifications:
Why Vericel?
EEO Statement
All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, age, disability, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of . Vericel Corporation is an Equal Opportunity/Affirmative Action Employer.
Vericel Corporation is VEVRAA federal contractor and desires priority referrals of protected veterans for job openings at all locations within the state.