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Bristol Myers Squibb Supervisor, Isotope Production in Indianapolis, Indiana

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.

The Supervisor - Isotope Production, reporting to the Associate Director - Radiopharmaceuticals, will be an integral part of bringing RayzeBio's innovative drug products to patients in need. As Supervisor - Isotope Production, you will be instrumental in implementing a novel isotope production program that will manufacture the clinical and commercial scale radioisotopes for RayzeBio's drug products. This individual will supervise a team of operators responsible for producing RayzeBio's radioisotopes under Good Manufacturing Practices (GMP). Additionally, you will be the front line in ensuring compliance with radiation safety requirements on the production floor.

*This is an onsite position at Rayzebio's Indianapolis, IN site

Job Responsibilities:

  • Oversee day-to-day operations for RayzeBio's radioisotope production (including scheduling, material preparation, line clearance, cleaning, equipment setup, and batch record execution) while ensuring compliance with GMP, NRC regulations, and management expectations.

  • Supervise and develop a team of high-performing operators.

  • Support Isotope Production Management with training of production staff.

  • Support and execute validation activities associated with isotope production at the clinal and commercial scale.

  • Work with cross-functional teams including Management, Radiochemistry and Engineering identifying opportunities to optimize production processes and enhance efficiency.

  • Support Isotope Production Management in compiling KPIs and investigation of quality events (deviations, OOS, etc.).

  • Support inventory management, including consumables, spare parts, cleaning supplies and personal protective equipment (PPE).

  • Promote a culture of safety and compliance with EHS and Radiation Safety programs.

  • Author and/or revise production technical documents (SOPs, forms, etc.) as needed.

Education and Experience:

  • Proven experience in a supervisory role.

  • 3 - 5 years' experience operating in a GMP environment.

  • Experience operating within hot cells and/or glove boxes strongly preferred.

  • Associate's or Bachelor's Degree in a STEM field is preferred.

Skills and Qualification:

  • Fluency in English.

  • Strong knowledge of GMP practice.

  • Knowledge of radiation safety principles.

  • Knowledge of radiopharmaceutical manufacturing.

  • Excellent professional ethics, integrity, and ability to maintain confidential information.

  • Well organized and detail oriented.

  • Strong interpersonal communication skills.

  • Motivated, adaptable, and able to work under pressure while meeting the needs of the production schedule.

#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 scienceā„¢ , 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: R1584742

Updated: 2024-09-13 03:01:18.427 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.

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