| Department
Of Quality Assurance |
| Title |
Quality Assurance Associate |
| Description |
The Quality Assurance department requires a Quality Assurance Associate who will report to the Manager of Quality Assurance (Manufacturing – 155 Innovation Drive facility). The QA Associate will ensure compliance to all applicable regulatory requirements along with Cangene’s Quality Management Systems – cGMP and ISO 9001. |
| Accountabilities |
The position duties will include, but are not limited to the following:
- Maintaining the Corrective Action program and other quality systems
- Conducting Quality Assurance investigations (Deviations, Out-of Specifications, etc.)
- Reviewing Manufacturing Operations and ensuring that they are carried out in accordance with applicable Standard Operating Procedure(s) and work instructions
- Performing line-opening and line-closing operations
- Liase with customers, as required, in carrying out the Quality Assurance functions associated with Cangene’s Contract Manufacturing Operations.
- Liase with other departments on Quality Assurance issues
- Carrying out the Quality Assurance functions associated with requests for product shipments.
- Carrying out other Quality Assurance functions as they may arise.
- Support Cangene in its mission of compliance and continuous improvement.
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| Management
Accountabilities |
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| Qualifications
|
Qualified candidates will have a B.Sc degree or equivalent with training in GMP/GLP/GCP regulations. The successful candidate will have a minimum of 2 years experience in the pharmaceutical industry, preferably in manufacturing, quality control, or quality assurance. Excellent written, verbal and interpersonal skills are required.
Interested applicants should submit a résumé and cover letter to Human Resources, 155 Innovation Drive, Winnipeg, Manitoba, R3T 5Y3 or fax to (204) 275-4021, or by email to hr@cangene.com.
Resumes will be accepted until August 5, 2010. The position, however, will remain open until successfully filled.
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