**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . Reporting to the Sr. Manager of Quality Control, the Quality Control Chemist will help support the establishment of a new Quality Control laboratory which supports RayzeBio's Radiopharmaceutical manufacturing facility in Indianapolis. The Quality Control Chemist will be responsible and/or providing support for the installation, commissioning, qualification, and validation of analytical and radiochemical equipment for the QC lab. Upon establishment of the laboratory and program, this position will utilize a wide range of analytical and radiochemical analyses to support the advancement and release of novel targeted radiopharmaceuticals from the R&D phase through clinical development to GMP commercial radiopharmaceutical production. Specifically, the quality control chemist will support the release of manufactured radiopharmaceuticals to support RayzeBio's clinical and commercial programs. ***This is an onsite position located at Rayzebio's Indianapolis, IN site*** **Key Responsibilities:** + Provide technical expertise and support for offsite vendors and RayzeBio MS&T and RA/QA teams in the installation and qualification of all laboratory equipment in a GMP environment. + Participate in method transfer activities from CMO or internal research facility to the production and QC teams, ensuring accuracy and reliability of data. + Assist in developing, verifying, and validating analytical methodologies in support of novel RayzeBio radiopharmaceuticals production in a GMP environment. + Assist in the writing of laboratory Standard Operating Procedures (SOP's) and related documents. + Assist in the routine calibration and maintenance of all laboratory equipment and materials. + Participate in troubleshooting and investigations of analytical issues, identify root causes, and implement corrective actions as required. + Develop and maintain appropriate documentation, including protocol, reports, and data analysis. + Participate and support instrument qualification, calibration, and maintenance activities. + Ensure compliance with GMP regulations, safety guidelines, and quality standards. + Work with RSO to ensure laboratory compliance with the radiation safety programs. + Provide technical support to other teams or business units as required. + Source and on-board analytical technologies as required. **Education and Experience:** + BS in Chemistry, Science, or relevant field with 5+ years of analytical or radiochemistry experience + MS in Chemistry, Science, or relevant field with 3+ years of analytical or radiochemistry experience + Experience with injectable pharmaceuticals or radiopharmaceuticals strongly preferred + Experience with HPLC, TLC, GC, Gamma Spec, and ICP all strongly preferred **Skills and Qualifications:** + Highly motivated and organized professional with the ability to work independently or in a team environment + Multi-disciplined scientist with GMP experience + Experience with root cause techniques such as 6 M's, 5 Why's, fishbone, or similar preferred + Very personable with strong communication skills + Excellent professional ethics, integrity, and ability to maintain confidential information + Must be comfortable working in a controlled environment with ionizing radiation and able to lift 40 lbs. **\#Rayzebio #LI-ONSITE** If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. **Uniquely Interesting Work, Life-changing Careers** With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. **On-site Protocol** BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. **Company:** Bristol-Myers Squibb **Req Number:** R1589155 **Updated:** 2025-02-08 02:40:30.558 UTC **Location:** Indianapolis-IN Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.