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RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals.

Summary

The Quality Assurance Incoming Material Disposition Senior Specialist is responsible for coordinating the receipt of deliverables to support the disposition of incoming materials such as consumables and raw materials at the RayzeBio Indianapolis, IN facility.  This position will perform review of the disposition deliverables to support disposition of materials and batches within the inventory management systems and assure materials comply with all RayzeBio policies, standards, procedures and global current Good Manufacturing Practice (cGMP).

The Senior Specialist provides Quality support and oversight for operations and disposition activities at the Indianapolis facility, including review and approval of Deviations, CAPAs, Change Controls, documents, and material disposition.    

Job Responsibilities

Essential duties and responsibilities include the following. Other duties may be assigned.

• Inspects consumables and raw materials per Standard Operating Procedures

• Build and maintain cross functional relationships to improve processes and resolve issues.

• Performs Quality Assurance review of documentation to support disposition of incoming materials.

• Works closely with supply chain and manufacturing with regards to discrepancy reporting, investigations and CAPAs associated with nonconforming material as well as the incoming material process.

• Drafts, revises, and approves procedural documents and material specifications.

• Performs review for department SOPs and Material Specification Documents.

• Supports warehouse personnel with concerns/issues with received material.

• Participates in Master Data management and supports master data for incoming materials.

• Leads the Indianapolis site Material Review Board

• Works with a cross functional team to process Supplier Change Notifications and determine appropriate actions needed.

• Responsible for the Supplier Complaint (SCAR) process for non-conforming material

• Coordinates with internal and external stakeholders to troubleshoot issues when required.

• Assist with and provide QA approval of investigations, CAPAs, change controls, validation documentation, and other related GMP documentation.

• Identify and report discrepancies from required work practices or procedures to management. 

• Make sound decisions by exercising judgment within generally defined practices and policies and applies appropriate notification to management as appropriate. 

• Participate as requested in the response team for audits and inspections by health authorities. 

Education and Experience

• BS/MS degree in science related field (including biology, biochemistry, chemistry, engineering, or related areas) is preferred

• Minimum of 5 years’ experience in quality assurance and/or compliance roles in the pharmaceutical industry.

• Experience with an Enterprise Resource Planning (ERP) system such as SAP is preferred.

• Experience working w