Scientist, Analytical Chemistry

Pfizer

Unknown, Unknown, USA
Base: $79,400.00 - $132,400.00; bonus/equity: 7.5%...
Qualitative and quantitative analyses of compounds
Establish analytical procedures
Interpret technical data
Conduct qualitative and quantitative analyses of various compounds and biologics to determine their properties during chemical syntheses, fermentation, or drug product development

Job Summary

  • Conduct qualitative and quantitative analyses of various compounds and biologics to determine their properties during chemical syntheses, fermentation, or drug product development.
  • Establish analytical procedures, interpret technical data, and develop scientific activities/projects to support team goals.
  • Actively participate and report progress in cross-functional project teams to meet customer expectations, project milestones, and Good Manufacturing Practices (cGMP) standards.

Matching Summary

Conduct qualitative and quantitative analyses of various compounds and biologics to determine their properties during chemical syntheses, fermentation, or drug product development.

Salary

Base: $79,400.00 - $132,400.00; Bonus/Equity: 7.5% of base salary; Benefits: Comprehensive and generous benefits and programs

Skills & Requirements

Must-have

  • Qualitative and quantitative analyses of compounds
  • Establish analytical procedures
  • Interpret technical data
  • Support team goals
  • Cross-functional project teams
  • Good Manufacturing Practices (cGMP)
  • Develop, qualify, validate, and transfer cell-based and immunoassays

Nice-to-have

  • Exceptional interpersonal skills
  • Proven track record of teamwork
  • Advanced analytical techniques and instrumentation
  • Effective verbal and written communication
  • Interact effectively with peers and leaders
  • Experience using common AI tools
  • Responsible AI practices

Key Requirements

  • BA/BS with at least 6 years of experience
  • MBA/MS with at least 4 years of experience
  • Interdisciplinary drug development teams
  • Developing analytical strategies and methods
  • Assessing quality and characteristics of biotherapeutics
  • Regulated environment such as Good Laboratory Practices (part of GxP)
  • Technical expertise in functional verification of design
  • Applicable industry test standards
  • Relevant regulatory guidance
  • Design Controls
  • Product Development Process

Work Rights

Permanent work authorization in the United States

Tailored Resume

Cover Letter