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Senior QA Specialist – I Location: El Segundo, CA (onsite) Duration: 18 months Description: Client is seeking a Senior Specialist of Quality Operations responsible for Product Disposition. This position will participate in Quality activities to ensure compliance with applicable quality objectives and regulatory requirements. This position is located at our El Segundo, CA site and report into the Associate Director of Quality Operations Responsibilities: Perform Product Disposition and Lot Closure. Includes commercial and clinical products. Review batch-related documentation and ensure resolution of issues to release product Review batch-related shipment documentation to ensure product shipment remained in control Provide QA oversight and review of deviations tied to lots. Ensure deviations are properly initiated, investigated and resolved in accordance with established disposition timelines. Provide QA oversight and (limited) approval of CAPAs. Ensures that associated CAPAs are initiated and resolved. Provide QA oversight and approval of change records. Ensures that change records are initiated and resolved. Support and participate in investigations, including batch record review. Ensure process control measures are in place and followed in product manufacturing Maintain metrics related to product disposition in support of the Management Review Generate and update procedures, forms and other documents As assigned, manage and provide QA oversight for other processes, including training, warehouse/inventory, redose, new product introductions, etc. Generate and report data for management Maintain production (finite), disposition, and team schedules Represent Disposition or QA Ops at plant and multi-site scheduling meetings Provide QA representation on projects and at team meetings Provide QA representation at multi-site disposition meetings Support and participate in inspections and audits Basic Qualifications: Master’s Degree and 5+ years of experience in GMP environment OR Bachelor’s Degree and 7+ years of experience in GMP environment OR High School Degree and 11+ years of experience in GMP environment Preferred Qualifications: Bachelor’s degree in the biological sciences or related field and minimum of 7 years progressive experience in a pharmaceutical, biotech, or biologics operation, or equivalent education/work experience. Working knowledge and ability to apply GMPs in conformance to U.S. and EU standards Ability to interpret and apply procedural and regulatory guidance in potentially ambiguous situations Ability to understand risk and provide phase-appropriate appropriate decisions Ability to effectively negotiate and build collaboration amongst individuals Good interpersonal skills Strong written communication skills Strong analytical skills Comfortable in a fast-paced small company environment and operate with minimal direction Ability to adjust workload based upon rapidly changing priorities As an equal opportunity employer, ICONMA provides an employment environment that supports and encourages the abilities of all persons without regard to race, color, religion, gender, sexual orientation, gender identity or express, ethnicity, national origin, age, disability status, political affiliation, genetics, marital status, protected veteran status, or any other characteristic protected by federal, state, or local laws.