Senior Associate Scientist, Radiochemist - Isotope Production - Bristol Myers Squibb
Indianapolis, IN
About the Job
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 Sr. Associate Scientist Radiochemist - Isotope Production, reporting to the Associate Director of Radiopharmaceuticals, will be an integral part of bringing RayzeBio's innovative drug products to patients in need. As Sr. Associate Scientist, Radiochemist - Isotope Production, you will be instrumental in implementing a novel isotope production program that will manufacture clinical and commercial scale radioisotopes for RayzeBio's drug products.
This individual will provide scientific and technical expertise to support the growth of the isotope production program, from initial establishment, scaling production, and GMP-compliant manufacturing. This individual is expected to support all aspects of isotope production including but not limited to radiochemical separations and processing, isotope purification, SOP development, training isotope production operators on the technology and process, and implementation of the site's radiation protection program.
*This is an onsite position located at Rayzebio's Indianapolis, IN site*
Key Responsibilities:
+ Provide radiochemistry expertise throughout the implementation of Rayzebio's isotope production program.
+ Assist in implementing the technology and operations needed to start up a new isotope production business unit.
+ Assist in the development of a GMP compliant radioisotope production process.
+ Work with cross-functional teams including Management, Operations and Engineering identifying opportunities to optimize production processes and enhance efficiency.
+ Assist in the generation and trending of isotope production KPIs.
+ Provide scientific and technical expertise to scale up GMP production.
+ Ensure compliance with GMP and NRC regulations, safety guidelines, and quality standards.
+ Mentor staff as an Authorized User on contamination control practices and implementing ALARA principles.
+ Work with RSO to ensure compliance with the radiation safety program and site radioactive material license.
+ Provide technical support to other teams or business units as required.
+ Draft laboratory Standard Operating Procedures (SOP's), protocols, reports and other related GMP documentation as required.
+ Support Rayzebio's corporate goals and initiatives where appropriate.
+ Up to 10% of travel may be required.
Education & Experience:
+ BS in Chemistry, Science, or relevant field with 3-5+ years of analytical or radiochemistry experience.
+ Experience with radiopharmaceutical development and/or production strongly preferred.
+ Experience with separations and solid-phase extractions strongly preferred.
+ Experience with alpha/gamma emitting radionuclides preferred.
Skills:
+ Highly motivated and organized professional with the ability to work both with a team and independently.
+ Multi-disciplined radiochemist with GMP experience.
+ Ability to express technical topics clearly and concisely.
+ Work effectively in a team - prioritizing shared goals, respecting diverse perspectives, and addressing technical disagreements constructively.
+ Excellent professional ethics, integrity, and ability to maintain confidential information.
#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: R1585689
Updated: 2024-10-08 02:16:50.309 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.
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 Sr. Associate Scientist Radiochemist - Isotope Production, reporting to the Associate Director of Radiopharmaceuticals, will be an integral part of bringing RayzeBio's innovative drug products to patients in need. As Sr. Associate Scientist, Radiochemist - Isotope Production, you will be instrumental in implementing a novel isotope production program that will manufacture clinical and commercial scale radioisotopes for RayzeBio's drug products.
This individual will provide scientific and technical expertise to support the growth of the isotope production program, from initial establishment, scaling production, and GMP-compliant manufacturing. This individual is expected to support all aspects of isotope production including but not limited to radiochemical separations and processing, isotope purification, SOP development, training isotope production operators on the technology and process, and implementation of the site's radiation protection program.
*This is an onsite position located at Rayzebio's Indianapolis, IN site*
Key Responsibilities:
+ Provide radiochemistry expertise throughout the implementation of Rayzebio's isotope production program.
+ Assist in implementing the technology and operations needed to start up a new isotope production business unit.
+ Assist in the development of a GMP compliant radioisotope production process.
+ Work with cross-functional teams including Management, Operations and Engineering identifying opportunities to optimize production processes and enhance efficiency.
+ Assist in the generation and trending of isotope production KPIs.
+ Provide scientific and technical expertise to scale up GMP production.
+ Ensure compliance with GMP and NRC regulations, safety guidelines, and quality standards.
+ Mentor staff as an Authorized User on contamination control practices and implementing ALARA principles.
+ Work with RSO to ensure compliance with the radiation safety program and site radioactive material license.
+ Provide technical support to other teams or business units as required.
+ Draft laboratory Standard Operating Procedures (SOP's), protocols, reports and other related GMP documentation as required.
+ Support Rayzebio's corporate goals and initiatives where appropriate.
+ Up to 10% of travel may be required.
Education & Experience:
+ BS in Chemistry, Science, or relevant field with 3-5+ years of analytical or radiochemistry experience.
+ Experience with radiopharmaceutical development and/or production strongly preferred.
+ Experience with separations and solid-phase extractions strongly preferred.
+ Experience with alpha/gamma emitting radionuclides preferred.
Skills:
+ Highly motivated and organized professional with the ability to work both with a team and independently.
+ Multi-disciplined radiochemist with GMP experience.
+ Ability to express technical topics clearly and concisely.
+ Work effectively in a team - prioritizing shared goals, respecting diverse perspectives, and addressing technical disagreements constructively.
+ Excellent professional ethics, integrity, and ability to maintain confidential information.
#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: R1585689
Updated: 2024-10-08 02:16:50.309 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.
Source : Bristol Myers Squibb