This Job Vacancy has Expired!

QA Auditor (GMP)

Posted on Jan 26, 2019 by OlonRicerca Bioscience

Ohio, OH
Research & Development
Immediate Start
Annual Salary
Full-Time

Essential Job Functions:

  • Ensure manufacturing and laboratory operations are performed in accordance with cGMPs under ICH Q7 and 21CFR210/211
  • Conduct in-process inspections of manufacturing and laboratory operations
  • Conduct audits of protocols, Master Batch Records, Production Batch Records, in-process and release laboratory data, cleaning records, test methods, and SOPs
  • Perform internal audits of systems and processes
  • Provide assistance with vendor qualification program and other quality-based systems

Educational Requirements:

  • Bachelor's degree in relevant field or Associate's degree with 2-4 years' experience

Work Experience/Skills Requirements:

  • Knowledge of auditing techniques
  • Ability to work independently and collectively with diverse groups comprised of chemists, engineers, and technicians

Preferred Skills:

  • Experience in quality control
  • Experience with QA GMP manufacturing experience (clinical API manufacturing desired)
  • Knowledge of pharmaceutical principles, practices, and their applications

Olon Ricerca Bioscience LLC. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.

Reference: 632748025