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)