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Corden Pharma - A Full-Service CDMO

QA Analytical Project Specialist

Corden Pharma - A Full-Service CDMO

Quality Assurance project specialist providing support in analytical methods and specifications for development and commercial products. Ensures compliance with GMP standards and offers quality leadership across projects.

Posted 5/14/2026full-timeBoulder • Colorado • 🇺🇸 United StatesMid-LevelSenior💰 $100,000 - $118,000 per yearWebsite

About the role

Key responsibilities & impact
  • Provides Quality Assurance related project assistance as it relates to analytical methods and specifications for both development and commercial products.
  • Responsible for providing strong Quality leadership and scientific/GMP information support to the plant-site as the Quality representative for new products/projects.
  • Supports analytical aspects of new product introduction.
  • Responsible for review and approval of protocols, and reports for stability and reference standards.
  • Serves as QA liaison on product/project implementation teams.

Requirements

What you’ll need
  • Bachelor’s Degree in Science with 5 years of Quality Assurance/Quality Control experience within the Pharmaceutical industry; or a combination of Pharmaceutical industry and academic experience with a strong knowledge in Analytical Chemistry.
  • Knowledge of cGMPs as they apply to documentation protocol and analytical method validation activities.
  • Ability to apply attention to detail, regulatory requirements, and a practical, defendable, logical approach to problem solving.

Benefits

Comp & perks
  • Benefits are those provided by the temporary agency.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
Quality AssuranceQuality ControlAnalytical ChemistrycGMPanalytical method validationdocumentation protocolprotocol reviewreport approvalstability standardsnew product introduction
Soft Skills
attention to detailproblem solvingleadershipcommunicationorganizational skills
Certifications
Bachelor’s Degree in Science