| Department
Of Validation |
| Title |
Computer Validation Coordinator / 1 Year Term |
| Description |
This position is responsible for planning, execution, and completion of validation projects involving computerized systems. The individual will report to the Validation Supervisor of Analytical and Computer Systems. |
| Accountabilities |
- Involved in the generation of protocols and reports for qualification of computer software and systems.
- Author validation documents, such as Validation Project Plans, IQ, OQ, PQ protocols, test procedures, summary reports and traceability matrices.
- Conducting or overseeing testing, as appropriate.
- Coordinate computer validation activities between internal departments and between Cangene and external facilities.
- Participate in the Change Control system to ensure maintenance of validated systems.
- Assist in the development, implementation and enforcement of validation policies and practices, with emphasis on computerized and automated systems.
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| Management
Accountabilities |
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| Qualifications
|
EDUCATION: Relevant university degree (science, computer sciences) or relevant college or technical diploma in computer / IT applications.
EXPERIENCE: 2+ years in a cGMP environment. Position requires good writing and communication skills, proficiency in MicroSoft Word and Excel; experience with computerized systems (LIMS™, TrackWise™, ClinTrace™) is an asset.
Interested applicants should submit a résumé and cover letter to, Human Resources, 155 Innovation, Winnipeg, Manitoba, R3T 5Y3, or fax to (204) 275-4021 or email to hr@cangene.com.
Résumés will be accepted until May 25, 2009. The position, however, will remain open until successfully filled.
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