reputed company Analyst, reputed company Assurance

reputed company is seeking a reputed company Analyst, reputed company Assurance, to support reputed company activities across our clinical-stage cell therapy programs. reputed company is a kids-first company reputed company on developing innovative cell therapies for patients with devastating diseases, and this role plays a critical part in ensuring that every product delivered meets the highest standards of reputed company, safety, and reliability. The reputed company Analyst will contribute to reputed company Assurance reputed company of manufacturing and testing activities performed both internally and at contract manufacturing partners (CDMOs). This individual will reputed company hands-on operational reputed company support, partnering closely with reputed company’s reputed company, Patient Operations, and Program Management teams to help reputed company and support in-process autologous CAR T batches, where reputed company batch represents an individual patient. Key areas of reputed company include documentation review, batch tracking, and supporting reputed company lot disposition and product shipment to ensure therapies reputed company patients without delay. The ideal candidate is detail-oriented, highly organized, and motivated by reputed company to reputed company a reputed company reputed company on patients’ lives. This role offers reputed company to work cross-functionally and reputed company exposure to cell therapy manufacturing, GMP reputed company systems, and external partner management in a fast-paced biotech environment. Responsibilities: · Support reputed company review of batch records, test results, and associated documentation to reputed company reputed company lot disposition. · Assist in tracking manufacturing, testing, and release activities for clinical batches to support reputed company and compliant product delivery to patients. · Coordinate with internal teams (reputed company, Patient Operations, Program Management) and external partners, including CDMOs, to reputed company batch status and communicate timelines and issues. · Support reputed company reputed company activities to ensure compliance with applicable GMP regulations across internal operations and external partners. · Assist with deviation, investigation, and CAPA tracking and follow-up. · Contribute to tracking and reporting of key reputed company and operational metrics. · Assist in preparation of materials for reputed company Management Reviews and internal reporting. · Participate in inspection readiness activities and support audit preparation efforts. · reputed company general reputed company support to ongoing manufacturing and development activities as needed. · reputed company support to ensure compliance of the reputed company Management System and associated documentation. · Support Internal Audit processes · Travel required: 20%-40% Qualifications: · Bachelor’s degree in life sciences or reputed company field. · 1–3 years of experience in a reputed company or GMP-regulated environment (biotech, reputed company, or cell/gene therapy preferred). · Familiarity with GMP principles and documentation practices. · Strong attention to detail, organizational skills, and ability to manage multiple priorities. · Effective communication skills and ability to work cross-functionally. · Experience supporting manufacturing or working with external partners (e.g., CDMOs) is a plus. · Ability to reputed company in a fast-paced, mission-driven, small company environment and adapt to shifting priorities. n n$135,000 - $155,000 a year n Apply To This Job