QA Reviewer

3 weeks ago

Pickering, Canada Weed Me Inc. Full time

**This position is a 12PM-8PM shift**

This is not a remote position
- Responsible for accurate and timely review of manufacturing batch records and other pertinent documents and records
- Receive batch record corrections from manufacturing personnel
- Communicate with appropriate personnel on missing documentation and error corrections
- Review of batch production records concurrently with production activities to ensure completeness and manage the correction process with the post-production team
- Review of production and analytical records and any supporting documentation to ensure compliance with GPP and Cannabis Regulations
- Review documentation for manufacturing activities in accordance with good documentation practices (GDP), including but not limited to: executed batch records, master batch records, product labels, and product specific document
- Independently executes batch record review for completeness, accuracy, and GPP/CR compliance
- Communicate effectively with cross functional departments to ensure on time delivery of QA review and disposition responsibilities
- Assist with initiation and completion of investigations, deviations and CAPAs appropriate and designated by QA Management
- Maintenance, and archival of batch records
- Help prepare batch release documentation for approval by QAP/ A/QAP
- Review and verify product labelling, case labelling, packed skids and verification prior to shipments
- Review incoming cannabis from third party suppliers in timely manner and ensure they are approved
- Perform potency verifications, compliance checks, label approvals
- Perform equipment and room cleaning verification, as necessary
- Organize and maintain the electronic storage of documents
- Training Management for organization including training matrices for all employees
- Create an ensure an organized environment for easy access to all documents in a timely manner

**Additional Duties**
- Ensure all employees are compliant with company SOPs, Good Production Practices, and Cannabis Regulations
- Perform routine document control activities including creation and/or revision, processing, routing and review of SOPs, BPRs, CAPAs, deviations, complaints, etc.
- Moving documents to draft, creating change requests, managing work flows etc.
- Create, use, and manage Quality spreadsheets, tracking sheets and checklists
- Assist with internal Quality audits of internal departments, as necessary.
- Provide guidance and train others on Quality System and Quality Assurance procedures
- Perform additional duties, as assigned
- Performs duties under limited supervision and according to standard operating and manufacturing procedures
- Evening or weekend work may be required

**Skills and Assets**
- Proficiency in the following internal systems and activities: SOP's, Change Controls, Deviations, Corrective Actions, Training records, and record retention is preferred
- Ability to quickly process complex information and make critical decisions with limited information is required
- Critical thinking, Self-sufficiency
- Experience in manufacturing, cannabis, pharma, or food industry is preferred
- Post-secondary education in science, or related field, is an asset
- Flexibility in schedule is preferred

**Job Types**: Full-time, Permanent

**Salary**: $42,000.00-$46,000.00 per year

**Benefits**:

- Dental care
- Life insurance
- Vision care

Schedule:

- 8 hour shift
- Evenings
- Evening shift
- Monday to Friday
- Weekend availability

Ability to commute/relocate:

- Pickering, ON: reliably commute or plan to relocate before starting work (required)

Work Location: One location

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