QA Reviewer L

2 weeks ago

Winnipeg, Canada IVC Vita Health Products Full time

**Review and Release of Starting Materials, Manufactured and Packed Items by IVC Vita Health & Items Received as Bulk, Intermediate Bulk and Finished Packed Products**:

- Conduct verifications on the documentation associated with received raw material, printed and non-printed packaging components.
- Conduct reviews on executed batch records and QC Laboratory records and all associated documentation Verify that Production and QC documentation are completed in compliance with approved SOPs.
- Ensure changes/ deviations in production or quality control have been approved according to QMS.
- Identify, report and resolve identified discrepancies and non-conformances. Initiate deviations, provide directions for any corrective actions that are required and complete any related tasks assigned.
- Verify the lot meets the release requirements are met for a release decision. Conduct the ERP system (M2M) transactions for the release of the lots.
- Collaborate with Product Owners, Developers and other QA team members as required on Acceptance criteria that need to be tested.
- Conduct any other M2M transactions as required.
- **Management of GMP Documentation**:

- Compile release documentation for customers (Certificate of Analysis, Certificate of Manufacture and Certificate of Packaging) and provide to both internal and external customers.
- Maintain and file all associated documentation appropriately for accessible retrieval.
- Provide the business with batch specific review and release status updates as required.
- Liaise with internal and external customers as required.
- Collect information for feedback to the daily direction setting priorities or others such internal meetings, as required.
- ** Project Management**:

- Participate in cross-functional teams on process control, improvement, and optimization projects; as well as participate in other continuous improvement projects.
- ** Audits**:

- Participate in internal, external as well as Regulatory audits.
- **Performs other related duties as assigned by Management.**

**Wage range: $24.00-25.50/hour**

**Experience**: Required
- 1 year(s): Working experience in production environment.
- 2 year(s): Experience in a GMP regulated environment and in quality assurance or manufacturing function.

**Behaviors**: Required
- Innovative: Consistently introduces new ideas and demonstrates original thinking
- Team Player: Works well as a member of a group
- Detail Oriented: Capable of carrying out a given task with all details necessary to get the task done well

**Motivations**: Required
- Flexibility: Inspired to perform well when granted the ability to set your own schedule and goals
- Goal Completion: Inspired to perform well by the completion of tasks

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