Analytical Development Specialist II — Radiopharmaceuticals

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

Benefits offered by this job

Health Coverage

401(k) plan

Paid Time Off

Flexible work options

Job summary

RayzeBio, a Bristol Myers Squibb company, is seeking a Senior Associate II in Analytical Development at our Indianapolis site. You will develop and validate parenteral radiopharmaceutical methods, transfer methods, and support regulatory documentation while collaborating across teams.

Ideal candidates have 3+ years in pharma, strong analytical technique knowledge (UHPLC/HPLC/GC/TLC/LC-MS), and GMP/radiopharma exposure. The role may require extended hours to meet manufacturing schedules.

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 radiopharmaceuticals or handling radioactive materials 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
• Prepare analytical test methods and method validation, verification, and transfer protocols and reports
• Work closely with other teams to ensure timely delivery of analytical results
• Participate in troubleshooting and investigations of analytical issues and implement corrective actions
• Develop and maintain notebooks, protocols, reports, SOPs and data analysis
• Participate in instrument qualification, calibration, and maintenance
• Ensure GMP compliance and radiation safety program adherence
• Provide technical support to other teams
• Source and onboard analytical technologies as required
• Perform other duties as required by management
• Work will be predominantly first shift, M-F, with potential extended hours or weekends

Skills

UHPLC/HPLC/GC/TLC

LC-MS/ICP/Gamma & Alpha Spectrometry

Analytical method development

Validation & transfer

AI tools for productivity

Microsoft Office Suite

Team collaboration

Education

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

Tools

Microsoft Office Suite

Lab software

Job description

RayzeBio, a Bristol Myers Squibb company, is seeking a Senior Associate II in Analytical Development at our Indianapolis site. You will develop and validate parenteral radiopharmaceutical methods, transfer methods, and support regulatory documentation while collaborating across teams.

Ideal candidates have 3+ years in pharma, strong analytical technique knowledge (UHPLC/HPLC/GC/TLC/LC-MS), and GMP/radiopharma exposure. The role may require extended hours to meet manufacturing schedules.