Vericel® Corporation
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Quality Control Analyst, I
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Vericel® Corporation Overview
At Vericel Corporation, we pioneer 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 performs 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. Responsibilities
Perform routine QC testing for raw materials, in‑process, DP, and stability samples using equipment such as balances, pipettes, pH meter, UV/Visible spectrophotometer, and plate reader, in accordance with SOPs and cGMP guidelines. Perform cell culture microbial and/or molecular assays. Perform routine Environmental Monitoring and utilities testing. Perform microbial limits, bioburden testing, and identify and trend microorganisms. Support laboratory activities, including glass washing, autoclaving, and general housekeeping. Assist in the review of QC data and provide summaries to management as needed. Report out‑of‑specification or out‑of‑trend results in a timely manner to ensure appropriate actions are taken. Calibrate and maintain QC general laboratory equipment, perform laboratory housekeeping, and prepare the laboratory for audits. Participate in transfer of methods from support groups to the QC laboratory. Coordinate departmental systems (inventory, documentation, equipment maintenance). Communicate inter‑departmentally and with outside contacts to solve technical issues. Exercise sound judgment and decision making when problem solving. Author and conduct periodic review of QC documents, including SOPs, protocols, and forms as needed. Initiate deviations and lab investigations as needed. Practice safe work habits and adhere to Vericel’s safety procedures and guidelines. Other duties as assigned. Qualifications
BS plus 0‑2 years’ industry experience in a cGMP lab environment, or AS, 2‑4 years’ industry experience. HS Diploma, 4+ years’ industry experience in a cGMP lab environment, or equivalent. Basic working knowledge of cGMP regulations and/or lab experience. Preferred Qualifications
1 year of experience in a cGMP lab environment. Proficient in Outlook, MS Word, Excel, and lab‑based data management systems (LIMs). Experience with microbiological testing or environmental monitoring. Experience in biotech, pharmaceutical, or other regulated industry. Why Vericel?
Cutting‑Edge Science: Work with a leading regenerative medicine product that is transforming patient care. Career Growth: Be a part of a growing organization with opportunities to expand your impact. Collaborative Culture: Work alongside a team of dedicated professionals who are passionate about improving lives. EEO Statement
All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, sexual orientation, gender identity, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of disability. Vericel Corporation is an Equal Opportunity/Affirmative Action Employer. Vericel Corporation is a VEVRAA federal contractor and desires priority referrals of protected veterans for job openings at all locations within the state. Seniority Level
Entry level Employment Type
Full‑time Job Function
Quality Assurance
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Quality Control Analyst, I
role at
Vericel® Corporation Overview
At Vericel Corporation, we pioneer 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 performs 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. Responsibilities
Perform routine QC testing for raw materials, in‑process, DP, and stability samples using equipment such as balances, pipettes, pH meter, UV/Visible spectrophotometer, and plate reader, in accordance with SOPs and cGMP guidelines. Perform cell culture microbial and/or molecular assays. Perform routine Environmental Monitoring and utilities testing. Perform microbial limits, bioburden testing, and identify and trend microorganisms. Support laboratory activities, including glass washing, autoclaving, and general housekeeping. Assist in the review of QC data and provide summaries to management as needed. Report out‑of‑specification or out‑of‑trend results in a timely manner to ensure appropriate actions are taken. Calibrate and maintain QC general laboratory equipment, perform laboratory housekeeping, and prepare the laboratory for audits. Participate in transfer of methods from support groups to the QC laboratory. Coordinate departmental systems (inventory, documentation, equipment maintenance). Communicate inter‑departmentally and with outside contacts to solve technical issues. Exercise sound judgment and decision making when problem solving. Author and conduct periodic review of QC documents, including SOPs, protocols, and forms as needed. Initiate deviations and lab investigations as needed. Practice safe work habits and adhere to Vericel’s safety procedures and guidelines. Other duties as assigned. Qualifications
BS plus 0‑2 years’ industry experience in a cGMP lab environment, or AS, 2‑4 years’ industry experience. HS Diploma, 4+ years’ industry experience in a cGMP lab environment, or equivalent. Basic working knowledge of cGMP regulations and/or lab experience. Preferred Qualifications
1 year of experience in a cGMP lab environment. Proficient in Outlook, MS Word, Excel, and lab‑based data management systems (LIMs). Experience with microbiological testing or environmental monitoring. Experience in biotech, pharmaceutical, or other regulated industry. Why Vericel?
Cutting‑Edge Science: Work with a leading regenerative medicine product that is transforming patient care. Career Growth: Be a part of a growing organization with opportunities to expand your impact. Collaborative Culture: Work alongside a team of dedicated professionals who are passionate about improving lives. EEO Statement
All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, sexual orientation, gender identity, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of disability. Vericel Corporation is an Equal Opportunity/Affirmative Action Employer. Vericel Corporation is a VEVRAA federal contractor and desires priority referrals of protected veterans for job openings at all locations within the state. Seniority Level
Entry level Employment Type
Full‑time Job Function
Quality Assurance
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