Sr Validation/CSV Specialists - Central USA Project

  • Contract

Company Description

QRC group is a life science firm dedicated to provide services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!

Job Description

To work in a Commissioning and Qualification project following ISPE Guidelines, and GAMP5 for computerized systems used by the pharmaceutical industry for C&Q activities. These activities include preparation, execution, distribution cycle for approvals, final report and close out of documents.

  • Hands on experience in the development and review of computer validation systems life cycle documentation, commissioning, traceability matrix, IQ, OQ, PQ protocols and report.
  • Hands on experience in the execution of CSV tests for PLC, HMI and software applications.
  • Tested skills developing Technical Reports and Technical Writing.

Qualifications

EDUCATION

  • BS Engineering and Sciences.
  • 3-5 years of working experience in a pharmaceutical production environment.

EXPERIENCE

  • Good interpersonal skills with an assertive and pro-active approach towards work.
  • Excellent communication skills (English).
  • Strong Technical Writing Skills; Excellent English writing skills

Additional Information

  • To work in the Central Zone of United States
  • Project duration: from 6 to 12 months
  • Willing to work as Independent Contractor (All-inclusive pay-rate)