Quality Control Analyst
at Tilray
Leamington, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 24 Apr, 2025 | Not Specified | 25 Jan, 2025 | 1 year(s) or above | Chemistry,Gpp,Management Skills,Employment Equity,Processing,Disabilities | 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:
Reporting to the Quality Control Manager, the Quality Control Analyst performs laboratory activities/projects including analysis of raw materials, finished products, and stability samples.
QUALIFICATIONS:
- A Bachelor’s degree or diploma with a major in chemistry required.
- 1-2 years analytical lab experience preferred.
- HPLC and GC experience preferred.
- Ability to read and follow documents (Standard Operating Procedures)
- Knowledge of cGMP requirements or GPP requirements an asset.
- Ability to work in a team environment.
- Detail-oriented and strong time management skills.
- Comfortable standing for long periods of time.
Tilray Brands welcomes applications from all qualified individuals and is committed to employment equity and diversity in the workplace. Accommodations are available for applicants with disabilities throughout the recruitment process. If you require accommodations for interviews or other meetings, please advise when submitting your application.
Please note that Tilray does not authorize, engage, or sponsor any consultants, agencies or organizations that seek certain personal or financial information from you (e.g. passwords, login ids, credit card information). Tilray does not charge any application, processing or onboarding fee at any stage of the recruitment or hiring process. When replying to emails, please ensure the sender name and email address match exactly. Please also ensure the Reply-To address matches the sending address exactly. If you are concerned about the authenticity of an email, letter, or call purportedly from, for, or on behalf of Tilray, please send an email inquiry to i n f o s e c @tilray.com
Responsibilities:
- Prepare samples and conduct testing as per standard test procedures by a variety of analytical techniques.
- Troubleshoot instrumentation and methodologies when mechanical or procedural difficulties occur.
- Follow laboratory safety rules and regulations.
- Ensure a high level of accuracy in sample preparation and analysis.
- Identifies and communicates non-conformances to Quality Control Supervisor and/or Manager.
- Assist with validation and verification of new methods as needed.
- Dispose of analyzed samples and follow proper chemical and waste procedures.
- Manage and maintain equipment, supplies, and cannabis inventory.
- Ensure laboratory cleanliness is maintained.
- Ensure the integrity and traceability of all generated and reported data.
- Perform any related tasks assigned by the Quality Control Supervisor and/or Manager
REQUIREMENT SUMMARY
Min:1.0Max:2.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Diploma
Chemistry
Proficient
1
Leamington, ON, Canada