**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 . 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 . As a Senior Packaging Engineer, you will play a crucial role in ensuring the efficiency, maintenance, and enhancement of packaging systems and infrastructure throughout the facility. You will be responsible for overseeing the design and implementation of manual and fully automated packaging systems that support GMP manufacturing processes, particularly for Radiopharmaceuticals at the Indianapolis site. In this position, you will lead the development and optimization of packaging processes, ensuring compliance with industry standards and regulatory requirements. Your role will involve troubleshooting and resolving issues related to packaging equipment and systems, as well as collaborating with cross-functional teams to support production needs. You will also assist in the commissioning, qualification, and validation of new packaging equipment, ensuring that all systems are fully operational and meet quality standards. Additionally, you will manage packaging spare parts and contribute to the creation of a Packaging Master Plan for the site, leveraging your technical expertise in packaging technologies, materials, and data management. **Job Responsibilities:** Essential duties and responsibilities include the following. Other duties may be assigned. + **Develop, Design, and Implement Packaging Systems:** Lead the development and integration of advanced packaging systems for the Indianapolis site. + **Develop, Design, and create specifications for packaging components & Related Materials:** This role will have the responsibility of packaging materials in addition to equipment and will work with supply chain to spec such components as kits, tubes, vials, stoppers, bags, and other equipment necessary for production working with validation to also validate such components and setting of min/max levels with supply chain. + **Develop Testing, Processes, and Consumables:** Develop testing such as crush testing for boxes, dye penetrate testing, label affixation testing, burst pressure testing, design of labels, booklets, text on labels, and development of kits for process. + **Documentation Management:** Create and maintain detailed documentation for packaging systems, including process flow diagrams, material specifications, and operational protocols. + **System Integration:** Collaborate with cross-functional teams to integrate packaging systems with Radiopharmaceutical Hotcells and other production equipment. + **Validation Support:** Assist the Validation team in developing and executing test plans to ensure the performance and reliability of packaging systems + **Continuous Improvement:** Monitor and optimize packaging processes to enhance reliability and reduce reliance on manual operations. + **Project Leadership:** Oversee and manage packaging projects from initial concept through deployment, ensuring timely execution and compliance with pharmaceutical and radiopharmaceutical standards. + **Collaboration:** Heavy collaboration with supply chain, regulatory, and quality on final packaging of product and tracking of processes. **Education and Experience:** + Minimum of a BS degree in Mechanical, Industrial, Packaging Engineering, or other applicable science. + 5-7+ years of experience as a Packaging Engineer + Experience working in a regulated industry such as radiopharmaceuticals, pharmaceuticals, biotechnology, healthcare, or medical device manufacturing is highly desirable. + Previous experience with serialization, label printing, label affixing machines, and burst testing of packaging is highly desired. + Prior experience with a SAP tyle system for supply chain management **Skills and Qualification:** + Highly motivated and organized professional able to work both independently and as part of a team + Ability to interpret technical drawings, schematics, and manuals for Packaging Systems. + Strong attention to detail is required + Very personable with strong communication skills + Excellent professional ethics, integrity, and ability to maintain confidential information + Understanding of DOT requirements + Understanding of QR code and barcode printing on vial, caps, and other consumables **Physical Demands:** While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision and distance vision. **Work** **Environment:** The noise level in the work environment is usually moderate. \#Rayzebio 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:** R1586402 **Updated:** 2024-11-13 03:12:21.764 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.