Senior Analytical Development Scientist (Radiopharmaceuticals)

Bristol Myers Squibb EU Policy; Indianapolis (IN); On-site; USD 82,000 - 100,000; Full time

Benefits offered by this job

Health coverage

401(k) plan

Paid time off

Stock opportunities

Job summary

RayzeBio, a Bristol Myers Squibb company, seeks a Senior Associate II, Analytical Development at its Indianapolis site. You will develop and validate analytical methods for parenteral radiopharmaceuticals, perform method transfers, and support GMP-compliant product development and commercialization.

The role requires 3+ years in pharma, proficiency in UHPLC/HPLC/GC/TLC/LC-MS and related techniques, plus GMP knowledge. First-shift work with potential extended hours may be needed.

Qualifications

• B.Sc. or M.Sc. in Analytical Chemistry, Pharmaceutical Sciences, or relevant scientific field.
• Three (3)+ years of pharmaceutical industry experience.
• Strong knowledge of analytical techniques such as UHPLC, HPLC, GC, TLC, ICP, LC-MS, Gamma Spectrometry, Alpha Spectrometry, and other analytical methods.
• Knowledge of GMP regulations, quality systems, and safety guidelines.
• Experience in method development, validation, verification, and transfer in the pharmaceutical or radiopharmaceutical industry.
• Experience with parenteral GMP manufacturing and/or radiopharmaceutical preferred but not required.

Responsibilities

• Develop and validate analytical methods for parenteral radiopharmaceutical products according to phase appropriate guidelines.
• Participate in method transfer activities from CDMO or internal research facility to QC team, ensuring data accuracy.
• Prepare analytical test methods and validation, verification, and transfer protocols and reports per guidelines (USP, EP, ICH).
• Work with other teams to ensure timely delivery of analytical results and support product development and commercialization.
• Troubleshoot analytical issues and identify root causes; implement corrective actions.
• Maintain documentation including notebooks, protocols, reports, SOPs, and data analysis.
• Participate in instrument qualification, calibration, and maintenance.
• Ensure GMP compliance, safety guidelines, and quality standards.

Skills

UHPLC

HPLC

GC

TLC

LC-MS

Gamma Spectrometry

Alpha Spectrometry

Analytical methods

Data analysis

Education

B.Sc./M.Sc. in Analytical Chemistry or Pharmaceutical Sciences

Tools

Instrument software

Microsoft Office

Job description

RayzeBio, a Bristol Myers Squibb company, seeks a Senior Associate II, Analytical Development at its Indianapolis site. You will develop and validate analytical methods for parenteral radiopharmaceuticals, perform method transfers, and support GMP-compliant product development and commercialization.

The role requires 3+ years in pharma, proficiency in UHPLC/HPLC/GC/TLC/LC-MS and related techniques, plus GMP knowledge. First-shift work with potential extended hours may be needed.