Senior Director, Analytical Development & Quality Control

Corvus Pharmaceutical

South San Francisco (CA)

On-site

USD 170,000 - 200,000

Full time

7 days ago
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Job summary

Corvus Pharmaceuticals seeks an Associate Director of Analytical Development & Quality Control to lead internal lab operations and mentor scientists. You will oversee analytical instrumentation, reference standards, and stability programs, while collaborating with CDMOs to advance late-stage programs.

Reporting to the Director of Analytical Development and Quality Control, you will drive method development, validation, OOS investigations, and regulatory submissions, with a strong emphasis on

Qualifications

  • Advanced degree in Chemistry, Pharmaceutics, or related field.
  • BS/MS with 10+ years or PhD with 7+ years of industrial experience in small molecule pharmaceutical development.
  • Expertise in HPLC method development is essential.
  • Experience with CDMOs/CROs and stability programs.

Responsibilities

  • Direction of internal laboratory operations and mentoring scientists.
  • Overseeing analytical instrumentation, reference standards, and stability programs.
  • Drive phase-appropriate analytical method development for late-stage programs.

Skills

HPLC method development
Analytical development
ICH guidelines knowledge
Data interpretation

Education

Advanced degree in Chemistry/Pharmaceutics or related field
MS/BS with 10+ years or PhD with 7+ years of industrial experience

Tools

Gas Chromatography
NMR
Mass Spectrometry
Dissolution testing
ICP-MS/OES
FTIR

Job description

Corvus Pharmaceuticals seeks an Associate Director of Analytical Development & Quality Control to lead internal lab operations and mentor scientists. You will oversee analytical instrumentation, reference standards, and stability programs, while collaborating with CDMOs to advance late-stage programs.

Reporting to the Director of Analytical Development and Quality Control, you will drive method development, validation, OOS investigations, and regulatory submissions, with a strong emphasis on

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