Cell Manufacturing Associate II Position Available In Miami-Dade, Florida

Cell Manufacturing Associate II Longeveron Miami, FL Job Details Full-time Estimated:

$59.9K – $79.2K a year 1 day ago Benefits AD&D insurance Paid holidays Health insurance Dental insurance Paid time off Employee assistance program Vision insurance 401(k) matching Qualifications CGMP Cell culture GMP Mid-level Bachelor’s degree Manufacturing Associate’s degree 2 years Communication skills Time management Full Job Description About Longeveron Longeveron Inc, a publicly traded (

NASDAQ:

LGVN), clinical-stage biotechnology company developing cellular therapies for aging-related and life-threatening conditions, with our headquarters located in Miami, FL. Our lead investigational product is laromestrocel, which is derived from culture-expanded medicinal signaling cells (MSCs) that are sourced from bone marrow of young healthy adult donors. We believe that by using the same cells that promote tissue repair, organ maintenance, and immune system function, we can develop safe and effective therapies for some of the most difficult rare diseases and conditions associated with aging. About the role The Cell Manufacturing Associate II reports to the Manager, Manufacturing and supports Longeveron’s cGMP manufacturing operations, performing intermediate-level manufacturing tasks to support cell therapy production. This position ensures adherence to cGMP standards and SOPs while performing cell culture, reagent preparation, and equipment operation. This role contributes to the development and optimization of manufacturing processes and supports junior staff, making it vital to our therapeutic production pipeline. What you’ll do Perform cell culture techniques, including isolation, expansion, and cryopreservation of cells. Prepare media, buffers, and other reagents with accurate measurements and thorough documentation. Operate and maintain manufacturing equipment such as bioreactors and centrifuges. Follow SOPs and batch production records to maintain detailed and compliant documentation. Participate in process development, optimization activities, and inventory management. Conduct routine quality control checks and uphold safety and quality standards. Assist in training Manufacturing Associate I staff and support broader team initiatives. Perform other tasks as assigned by the supervisor. What you’ll need Associate’s degree in a scientific discipline is required; bachelor’s degree preferred. Minimum 2 years of experience in a cGMP manufacturing environment. Proficiency in aseptic processing and advanced cell culture techniques. Strong attention to detail and ability to follow detailed instructions and SOPs. Critical thinking, time management, communication and teamwork skills are required. Demonstrated ability to troubleshoot and resolve basic manufacturing issues. Must be process oriented, safety and quality-focused. Ability Ability to travel up to 10% based on the needs of the business. This role is not available for sponsorship including I-983 participation What we offer Medical, dental and vision benefits (employee premiums covered at 100% & 90% coverage for spouse/family) 401(k) plan with company match Generous paid time off plan and company holidays 2 paid company shutdowns (winter and summer) Employee assistance program Life and supplemental AD&D insurance Physical and Environmental Requirements This role works in a clinical manufacturing lab and involves routine use of manufacturing equipment following GMP protocols and may include exposure to cryogenic materials and biological agents. The role involves working in a clean room environment that requires the ability to follow gowning procedures and adherence to strict hygiene standards, working with a team of operators, receiving comprehensive training and support from the operations team. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job: Ability to remain standing for extended periods within a cleanroom or lab setting. Frequent use of laboratory equipment and sterile manufacturing supplies. Regular lifting of containers or materials up to 25 pounds. Must be able to wear cleanroom gowning and PPE for extended periods. We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Longeveron Inc will not pay fees to any third-party agency or firm associated with unsolicited resumes. Longeveron is an equal opportunity employer that is committed to diversity and inclusion in the workplace. At Longeveron, we prohibit harassment of any kind and any form of discrimination including but not limited to discrimination based on race, color, sex, religion, marital status, sexual orientation, national origin, disability, veteran status, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. 0HHe3Q40cV