JobHabor
Location
East Windsor, NJ, United States
Workplace
Employment
Full Time
Salary
Apply on the employer’s site

Posted 11y ago

Job Requirement

  • Create and establish a scientific approach to the company quality system.
  • Perform review and release of API and excipients in support of manufacturing.,
  • Establish training and audit programs, as well as the review of SOPs, investigations, specifications, methods, validation reports, cleaning verification reports, analytical reports and manufacturing records.
  • Review and approve Master documents such as Master Batch Records, In-process forms, Method Qualification Protocols, Method Validation Protocols, test methods, reference standards and other related documents.
  • Provides guidance and training for other Quality Assurance staff in the accomplishment of Quality Assurance operation activities.
  • Act as company’s representative during regulatory agencies and customer inspections

Qualifications

  • BS degree in Chemistry, Life Science or related discipline and a minimum 1-5 years of QA/validation experience in an FDA regulatory Industry.
  • Familiar to solid dosage pharmaceutical manufacturing process with thorough understanding in GMP
  • Strong technical writing skills and the ability to clearly express ideas in English.
  • Local Candidates preferred.

732-429-1858

eayache @ irionline.com

http://www.irionline.com

Skills

  • SOPS
  • HTTP

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