Quality Assurance Associate
at Tilray
Leamington, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 31 Jan, 2025 | Not Specified | 01 Nov, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
JOB SUMMARY:
This is an incredible opportunity to be an integral part of one of the fastest growing, and best companies in the world. At Aphria, we are dedicated to making a difference in the lives of our patients and consumers. As industry leaders committed to offering clean, safe, and pure cannabis products, we engage in a collaborative culture that is fast paced, dynamic and highly motivating. If you’re looking to thrive in a new, rapidly growing and innovative space, we would love to hear from you. We are currently seeking a strong individual to join our Quality team.
Shift Schedule: Monday - Friday (Day shifts)
- This will be a 1-year contract.
Responsibilities:
- Continually monitor GPP regulatory requirements for the Cannabis Act and Cannabis Regulations and their associated regulations such as those for Natural Health Products.
- Assist all functional departments on establishing systems to eliminate GMP/GPP gaps.
- Support and maintain systems to ensure quality of products as defined through internal Good Production Practices and established Standard Operating Procedures.
- Communicate, educate and support the quality requirements to all operational departments.
- Create, review and maintain Standard Operational Procedures, investigate non-conformances/deviations and customer complaints as it relates to quality.
- Participate in the initiation and writing of change controls or controlled documents as needed to ensure defined quality objectives are met.
- Perform inspection and verification on label print in a detailed manner.
- Perform Internal Audits on various departments to ensure Quality compliance and excellence.
- Perform inspection on componentry, incoming and internal product and finished good products.
- Work directly with other team members to complete tasks as assigned.
- Read, understand and follow safe work procedures.
- Other duties as assigned
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Software Testing, Clinical Pharmacy
Graduate
Proficient
1
Leamington, ON, Canada