BioSpace
Manufacturing Associate 2 – Cell Therapy
BioSpace, Redwood City, California, United States, 94061
Overview
Manufacturing Associate 2 – Cell Therapy Join to apply for the Manufacturing Associate 2 – Cell Therapy role at BioSpace. Adicet Bio, Inc. is a clinical stage biotechnology company discovering and developing allogeneic gamma delta T cell therapies for autoimmune diseases and cancer. Adicet is advancing a pipeline of “off-the-shelf” gamma delta T cells, engineered with chimeric antigen receptors (CARs), to facilitate durable activity in patients. For more information, please visit our website at https://www.adicetbio.com. MANUFACTURING ASSOCIATE II – CELL THERAPY We are seeking a highly motivated and detail-oriented individual with a strong background in cell process development and/or manufacturing. The Manufacturing Associate II will report to the Director of Manufacturing and help support daily GMP manufacturing operations for allogeneic CAR T cell therapies. Responsibilities
Execute manufacturing processes in compliance with GMP, GDP, and safety requirements. Assist with troubleshooting complex and non-routine equipment issues. Initiate and support deviation investigations and contribute to CAPAs. Author and revise SOPs to drive operational excellence. Collaborate cross-functionally to ensure readiness for manufacturing runs, including materials, equipment, and documentation. Oversee and participate in execution of cellular drug product and viral vector manufacturing in a GMP cleanroom environment per SOPs and batch records. Operate and troubleshoot bioprocess equipment such as Sepax, LOVO, CliniMACS, functionally closed system bioreactors, TFF systems, and controlled-rate freezers. Partner with Quality Assurance, Facilities, and supervisors to ensure run readiness (materials, equipment, documentation, and training). Collaborate with MS&T to refine manufacturing batch records and with Supply Chain to manage bill-of-materials and ordering. Perform environmental and personnel monitoring as needed. Participate in Quality Management System activities, including deviations, CAPAs, and document control. Maintain compliance with all safety protocols and best practices. In this role, you will apply expertise across a variety of production activities, including cell processing, reagent preparation, aseptic techniques, equipment operation and monitoring, cell counting, product sampling, and routine facility/equipment sanitization. You should be comfortable working both independently on routine tasks and collaboratively on more complex operations, escalating issues as appropriate. Qualifications
Bachelor’s degree in biological sciences, engineering, or related discipline, plus 1–2 years of experience in clinical processing and/or cell culture operations (preferably in a GMP environment); or equivalent combination of education and experience. GMP cleanroom experience in cell therapy manufacturing, including gown qualification, aseptic technique, materials kitting, and aseptic material transfer. Strong background in cell therapy or CAR T manufacturing preferred. Familiarity with GMP, GDP, and FDA regulatory guidelines. Process-oriented mindset with strong attention to detail and analytical skills for risk identification. Excellent verbal and written communication skills; able to collaborate effectively across teams and levels. Self-motivated, adaptable to shifting priorities, and comfortable in a fast-paced, small-company environment. Proficiency with MS Word, Excel, PowerPoint, and Outlook. Compensation and Work Arrangement
Hourly Pay: $41.35—$57.21 USD. Adicet fosters a collaborative, high-performing environment by prioritizing in-person engagement. Employees are required to be onsite at least three days per week (Tuesday–Thursday mandatory), with some roles requiring full-time onsite presence. About Adicet
Adicet is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. We offer a competitive compensation package including base salary, annual cash bonus, long-term incentives (equity), Employee Stock Purchase Plan (ESPP) and a 401(k) with ROTH and a 4.5% Company match. We also provide comprehensive health plans (medical, dental, vision), Flexible Health and Commuter Spending Accounts (FSA) and a company matched Health Savings Account (HSA). Additional benefits include life, AD&D, short and long-term disability insurance, and various voluntary programs. Generous paid time-off includes holidays, winter break, vacation, sick time, and parental leave. Onsite facilities include an gym, parking with EV charging, free shuttle, and subsidized lunches. Adicet is located in a state-of-the-art facility and is dedicated to creating the best possible office experience for employees.
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Manufacturing Associate 2 – Cell Therapy Join to apply for the Manufacturing Associate 2 – Cell Therapy role at BioSpace. Adicet Bio, Inc. is a clinical stage biotechnology company discovering and developing allogeneic gamma delta T cell therapies for autoimmune diseases and cancer. Adicet is advancing a pipeline of “off-the-shelf” gamma delta T cells, engineered with chimeric antigen receptors (CARs), to facilitate durable activity in patients. For more information, please visit our website at https://www.adicetbio.com. MANUFACTURING ASSOCIATE II – CELL THERAPY We are seeking a highly motivated and detail-oriented individual with a strong background in cell process development and/or manufacturing. The Manufacturing Associate II will report to the Director of Manufacturing and help support daily GMP manufacturing operations for allogeneic CAR T cell therapies. Responsibilities
Execute manufacturing processes in compliance with GMP, GDP, and safety requirements. Assist with troubleshooting complex and non-routine equipment issues. Initiate and support deviation investigations and contribute to CAPAs. Author and revise SOPs to drive operational excellence. Collaborate cross-functionally to ensure readiness for manufacturing runs, including materials, equipment, and documentation. Oversee and participate in execution of cellular drug product and viral vector manufacturing in a GMP cleanroom environment per SOPs and batch records. Operate and troubleshoot bioprocess equipment such as Sepax, LOVO, CliniMACS, functionally closed system bioreactors, TFF systems, and controlled-rate freezers. Partner with Quality Assurance, Facilities, and supervisors to ensure run readiness (materials, equipment, documentation, and training). Collaborate with MS&T to refine manufacturing batch records and with Supply Chain to manage bill-of-materials and ordering. Perform environmental and personnel monitoring as needed. Participate in Quality Management System activities, including deviations, CAPAs, and document control. Maintain compliance with all safety protocols and best practices. In this role, you will apply expertise across a variety of production activities, including cell processing, reagent preparation, aseptic techniques, equipment operation and monitoring, cell counting, product sampling, and routine facility/equipment sanitization. You should be comfortable working both independently on routine tasks and collaboratively on more complex operations, escalating issues as appropriate. Qualifications
Bachelor’s degree in biological sciences, engineering, or related discipline, plus 1–2 years of experience in clinical processing and/or cell culture operations (preferably in a GMP environment); or equivalent combination of education and experience. GMP cleanroom experience in cell therapy manufacturing, including gown qualification, aseptic technique, materials kitting, and aseptic material transfer. Strong background in cell therapy or CAR T manufacturing preferred. Familiarity with GMP, GDP, and FDA regulatory guidelines. Process-oriented mindset with strong attention to detail and analytical skills for risk identification. Excellent verbal and written communication skills; able to collaborate effectively across teams and levels. Self-motivated, adaptable to shifting priorities, and comfortable in a fast-paced, small-company environment. Proficiency with MS Word, Excel, PowerPoint, and Outlook. Compensation and Work Arrangement
Hourly Pay: $41.35—$57.21 USD. Adicet fosters a collaborative, high-performing environment by prioritizing in-person engagement. Employees are required to be onsite at least three days per week (Tuesday–Thursday mandatory), with some roles requiring full-time onsite presence. About Adicet
Adicet is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. We offer a competitive compensation package including base salary, annual cash bonus, long-term incentives (equity), Employee Stock Purchase Plan (ESPP) and a 401(k) with ROTH and a 4.5% Company match. We also provide comprehensive health plans (medical, dental, vision), Flexible Health and Commuter Spending Accounts (FSA) and a company matched Health Savings Account (HSA). Additional benefits include life, AD&D, short and long-term disability insurance, and various voluntary programs. Generous paid time-off includes holidays, winter break, vacation, sick time, and parental leave. Onsite facilities include an gym, parking with EV charging, free shuttle, and subsidized lunches. Adicet is located in a state-of-the-art facility and is dedicated to creating the best possible office experience for employees.
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