Quality Documentation Associate
2 weeks ago
The primary goal of the Quality Documentation Associate is to assist the QA and the QC Specialists in the creation, the review and the upload of MEDISCA’s product related documentation. Other duties may be assigned by Quality Management. If you are an enthusiastic self-starter, goal driven, love quality and have an interest in the pharmaceutical industry, then we are looking for you
**The opportunity**:
Review and Creation of MEDISCA Quality Documentation
- Review of Manufacturer Certificate of Analysis
- Review of Compendia testing requirements
- Review of Laboratory Certificate of Analysis
- Creation and uploading of MEDISCA Certificate of Analysis
- Creation, Revising and Uploading of MEDISCA Specifications
- Creation and Updating of Medisca Labels
Production Support (On an as needed basis)
- Review and approved Packaging Masters
- Perform Lab Audits
- Inspect and Release Finished Goods as per procedures.
- Maintain and archive receiving reports
Any other duties assigned by Quality Management.
**You**:
- Minimum Cegep/College degree in Science
- Experience in a Quality Assurance / Quality Control environment is considered an asset
- Knowledge of Health Canada’s current Good Manufacturing Practices (cGMP’s) is considered an asset
- Excellent communication skills required; fluent English and French (oral & written)
- Attention to detail is a must; accountable for his/her work
- Proven decision making and problem solving skills
- Knowledge of Microsoft Office (Word, Outlook, Excel) required; Syspro/MasterControl an asset
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