RayzeBio, Inc Posted July 30, 2026

Associate Scientist I, Quality Control, Isotope Production

Indianapolis, United States Full time
Quality Associate
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RayzeBio, Inc is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Life at BMS

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact, on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio:  https://careers.bms.com/rayzebio/

Summary

Reporting to the Quality Control Supervisor – Isotope Production, the associate scientist will execute testing in the Quality Control laboratory which supports RayzeBio’s Isotope Production process in Indianapolis. This position will conduct inspections and testing of raw materials, in-process controls, and finished products, ensuring compliance with specifications and regulatory standards. Specifically, the Associate Scientist will support the release of isolated isotopes manufactured at RayzeBio in support of clinical and commercial drug programs.

 

Job Responsibilities

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

Perform routine and non-routine analyses according to validated/verified methods to support RayzeBio isotope production.

Record data and analyze results quickly and accurately to ensure timely completion of final product testing and release.

Assist in the development, review, and continuous improvement of laboratory Standard Operating Procedures (SOPs) and related documents.

Execute, document, and close out records with attention to detail, ensuring appropriate recordkeeping is maintained.

Participate in troubleshooting and investigations of analytical issues, identify root causes, and implement corrective actions as required.

Assist in the routine calibration and maintenance of all laboratory equipment and materials.

Develop and maintain appropriate documentation, particularly data analysis.

Participate in and support instrument qualification, calibration, and maintenance activities.

Ensure compliance with GMP regulations, safety guidelines, and quality standards.

Partner with the Radiation Safety Officer (RSO) to ensure laboratory compliance with radiation safety programs.

Provide technical support to other teams or business units as required.

Review laboratory data and documentation to support timely disposition and release of isotope production batches.

This is primarily a first-shift position. Work outside normal first-shift hours is expected on a periodic basis due to the time-sensitive nature of the product, including evening work when required.

 

Education and Experience

Bachelor's degree in Chemistry or a related scientific discipline, or an equivalent combination of education and experience, with 0–3 years of experience in analytical chemistry, radiochemistry, or a related field.

Knowledge of, and experience with, quality systems and documentation practices (e.g., GMP, ISO) is preferred.

Skills and Qualifications

Highly motivated and organized professional with the ability to work independently or in a team environment

Experience or training in a laboratory environment utilizing Good Laboratory Practices (GLP).

Ability to manage multiple projects and competing priorities simultaneously.

Familiarity with sample preparation and general bench chemistry techniques

Strong interpersonal, written, and verbal communication skills.

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

Uses AI tools to enhance individual productivity and quality of work

 

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 40 pounds. Specific vision abilities required by this job include close vision and distance vision.

#LI-Onsite

This position requires working in a laboratory environment where protective clothing, gloves, and safety glasses must be worn while handling radioactive materials.

 

Work Environment

The noise level in the work environment is usually moderate.

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Compensation Overview:

Indianapolis - RayzeBio - IN: $31.07 - $37.64per hour


The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.

Benefits:

Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).

U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.

Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.

Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.

U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits

RayzeBio and Bristol Myers Squibb

RayzeBio was acquired by Bristol Myers Squibb (BMS) in 2024 and is a wholly-owned subsidiary of BMS; however, RayzeBio will continue to operate as a standalone organization.

Supporting People with Disabilities

BMS and RayzeBio are 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/eeo-accessibility  to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS and RayzeBio will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only:  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/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at  https://careers.bms.com/fraud-protection .

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at  TAEnablement@bms.com with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1604723 : Associate Scientist I, Quality Control, Isotope Production

Job details

Seniority
Associate
Function
Quality
Therapeutic area
Not listed
Location
Indianapolis, United States
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 265 comparable Associate Quality roles across 71 biopharma companies.

265Comparable roles tracked
240Currently active
71Companies hiring similar roles
29Countries represented

Salary context

49 of 265 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Quality Associate Scientist · Merck KGaA $25/hr – $39/hr (≈ $52,000–$81,120/yr)
Highest disclosed · Senior Manager, Quality Assurance · Gilead Sciences, Inc. $157,590/yr – $203,940/yr
Peer group range $66,560 – $180,765 (median $156,390)

Where these roles are based

Top locations among the 265 comparable roles

United States89
Germany26
China20
France14
India14
Ireland13

+ 23 more countries

Seniority mix

265 of 265 peers have a known seniority level

Manager164
Intern/Fellow/Postdoc59
Associate42

Therapeutic area mix

0 of 265 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
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60%similar
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60%similar
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60%similar
Perrigo Eau Claire, United States Associate
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60%similar
Devens Devens, United States Associate
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Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
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ModernaTX, Inc. · Norwood, United States · Associate
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.