Senior Analytical Development Scientist - Radiopharma

Bristol-Myers Squibb

Indianapolis (IN)

Vor Ort

USD 82.000 - 100.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

RayzeBio, a Bristol Myers Squibb company, seeks a Senior Associate II, Analytical Development to join our Indianapolis site. You will develop and validate analytical methods for parenteral radiopharmaceutical products and participate in transfers, verification, and stability testing to support product development.

You'll work with UHPLC, HPLC, GC, LC-MS, and other techniques, ensuring GMP compliance and accurate documentation, reporting to the Manager of Analytical Development.

Qualifikationen

  • Three (3) or more years of pharmaceutical industry experience.
  • Strong knowledge of UHPLC, HPLC, GC, LC-MS, and related analytical methods.
  • Experience with method development, validation, verification, and transfer.
  • Familiarity with GMP regulations and safety guidelines.

Aufgaben

  • Develop and validate analytical methods for parenteral radiopharmaceutical products.
  • Participate in method transfer activities, ensuring accuracy and reliability of data.
  • Prepare validation and transfer protocols and reports per USP, EP, ICH guidelines.
  • Maintain documentation and assist with instrument qualification and maintenance.
  • Ensure compliance with GMP, safety guidelines, and radiation safety programs.

Kenntnisse

UHPLC
HPLC
GC
LC-MS
Gamma Spectrometry
Alpha Spectrometry
Analytical Method Development
Data Analysis

Ausbildung

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

Tools

Laboratory software

Jobbeschreibung

RayzeBio, a Bristol Myers Squibb company, seeks a Senior Associate II, Analytical Development to join our Indianapolis site. You will develop and validate analytical methods for parenteral radiopharmaceutical products and participate in transfers, verification, and stability testing to support product development.

You'll work with UHPLC, HPLC, GC, LC-MS, and other techniques, ensuring GMP compliance and accurate documentation, reporting to the Manager of Analytical Development.

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