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Manufacturing Associate

Job

Neurona Therapeutics

South San Francisco, CA (In Person)

$77,082 Salary, Full-Time

Posted 6 days ago (Updated 4 days ago) • Actively hiring

Expires 7/24/2026

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Job Description

Manufacturing Associate Neurona Therapeutics South San Francisco, CA Job Details $32 - $39 an hour 9 hours ago Qualifications Manufacturing equipment maintenance Raw material quality management Cell line culture Engineering equipment malfunctions diagnostics Content creation for technical audiences Investigations regulatory compliance Laboratory equipment performance testing and validation Technical documentation Pharmaceutical regulatory compliance Preventive action implementation Engineering Laboratory instrument validation Technical writing within manufacturing Production deviation management Engineering process optimization Corrective and preventive actions (CAPA) Cleanroom protocols Mid-level Incident Escalation Laboratory equipment calibration Industrial equipment troubleshooting Factory operations documentation Manufacturing standard operating procedures Manufacturing facility Policy & process development Bachelor's degree in engineering Production validation processes Quality control documentation Continuous improvement Technology transfer (scale-up process)
Full Job Description Manufacturing Associate Location:
South San Francisco, CA, 94080 About Neurona Therapeutics Neurona Therapeutics is a clinical-stage biotechnology company based in South San Francisco focused on the development of allogeneic, regenerative neural cell therapies for neurological disorders. Neurona's lead product candidate, rezanecel (formerly
NRTX-1001
), is an investigational cell therapy comprising GABAergic interneurons designed to provide a novel, non-tissue-destructive treatment approach for drug-resistant mesial temporal lobe epilepsy (MTLE). Rezanecel is currently being evaluated in ongoing multicenter Phase 1/2 clinical trials for patients with drug-resistant unilateral and bilateral MTLE and has demonstrated encouraging safety and efficacy results to date. The U.S. Food and Drug Administration (FDA) granted Regenerative Medicine Advanced Therapy (RMAT) designation to rezanecel in 2024, and the European Medicines Agency (EMA) granted Priority Medicines (PRIME) designation in 2025. Neurona is preparing to initiate its Phase 3 EPIlepsy Cell Therapy (EPIC) trial, a randomized, sham-controlled, double-blind study designed to further evaluate rezanecel in adults with drug-resistant MTLE. Through its pioneering cell therapy platform, Neurona is advancing innovative treatments intended to restore neural circuit function and address serious neurological disorders with significant unmet medical need. Position Summary Our ideal candidate is a self-motivated individual who has a passion for manufacturing in a research and production setting. This is a fantastic opportunity to join a small team, work on transformative cell therapies, and take part in building an exciting, science-driven company. Responsibilities Execute cGMP manufacturing operations on the production floor. Support process transfer, implementation, and continuous improvement activities. Maintain laboratories and manufacturing areas, including equipment maintenance, calibration, cleaning, and documentation. Follow all safety, quality, and compliance requirements. Support equipment commissioning, qualification, validation, and ongoing lifecycle activities. Support raw material and vendor qualification activities. Troubleshoot equipment, materials, and manufacturing process issues. Write and revise controlled documents, including SOPs, manufacturing procedures, forms, and technical reports. Support investigations, deviations, non-conformances, and CAPA activities. Collaborate with Quality, Manufacturing, Regulatory, and CMO partners to support manufacturing operations and product supply. Escalate issues that may impact safety, quality, equipment performance, or product supply. Present manufacturing data and operational updates at departmental meetings. Work effectively both independently and within cross-functional teams. Required Qualifications Bachelor's degree in science or engineering with 2+ years of industrial experience or equivalent. Preferred Qualifications 2+ years of industrial experience in cGMP operations. Knowledge of cell culture operations and bioreactors. Knowledge of analytical equipment and computers. Knowledge of CFRs and cGMP requirements and ability to interpret and apply the knowledge. Aseptic processing, cleanroom operations, and cell culture experience a plus. Ability to independently collaborate with outside vendors. Understanding of analytical methods for in-process testing requirements in the manufacturing area. Possess excellent troubleshooting skills, technical writing capability, presentation and interpersonal skills. Able to take initiative to improve work processes, develop innovative scientific methodologies and approaches to enhance process productivity. This job description is not exhaustive and not intended to cover all activities of the position. Duties, responsibilities and activities may change, or new ones may be assigned at any time with or without notice. Neurona is proud to be an equal opportunity employer and will consider all qualified applicants for employment. Recruitment Fraud Notice We are aware of active recruitment scams using the Neurona name, where individuals pose as our recruiters or post fake remote job openings and make fraudulent job offers online. Please note, that we will never make an offer of employment without conducting multiple rounds of face-to-face interviews using secure video-conferencing technology. Additionally, we will never ask candidates to cash checks or make any payment to be considered for a position.