Tilray Brands is a leading global cannabis-lifestyle and consumer packaged goods company with operations in Canada, the United States, Europe, Australia, and Latin America. The company is committed to changing people's lives for the better by inspiring and empowering the worldwide community to live their very best life, offering products that meet the needs of mind, body, and soul, and evoke a sense of wellbeing. Tilray’s mission is to be a trusted partner for patients and consumers by providing a cultivated experience and promoting health and wellbeing through high-quality, differentiated brands and innovative products. As a pioneer in cannabis research, cultivation, and distribution, Tilray supports over 20 brands across more than 20 countries, including comprehensive cannabis offerings, hemp-based foods, and alcoholic beverages.
Are you looking to develop your career at the forefront of a rapidly expanding industry?
Ready to apply your talents to make a positive difference in the lives of patients around the globe?
The Quality Control Manager will be responsible for performing analytical chemistry quality control testing to ensure the highest quality, potency, and purity of Tilray products.
Role and Responsibilities
* Perform analytical chemistry tests for quality control samples.
* Assist in the development and maintenance of validated quality control methods.
* Acquire, set up, and validate QC Lab equipment.
* Manage laboratory processes and data effectively.
* Maintain high-quality laboratory documentation in accordance with regulatory guidance and SOPs.
* Document test results, maintain batch records, and coordinate with the VP or Chief Science Officer for batch approval and release.
* Perform calibration and maintenance on laboratory instruments.
* Ensure proper disposal of hazardous chemical waste.
* Monitor use and inventories of laboratory chemicals and supplies, maintaining appropriate levels.
* Supervise laboratory technicians in the quality control laboratory.
* Identify opportunities for improvement of analytical methods.
* Develop, author, implement, and revise all Quality Control SOPs.
* Stay updated with technical advances in analytical and pharmaceutical sciences.
* Keep abreast of current trends in regulatory requirements in Quality Control.
* Review analytical methods, validation protocols, reports, and transfer protocols.
* Review and revise release and stability specifications as necessary.
* Review and approve all analytical data supporting product testing, stability, and release.
Qualifications and Requirements
* Degree in Chemistry, Biochemistry, or Biotechnology with at least 3 years of experience.
* A minimum of 5 years’ experience with HPLC, GC-MS, and other analytical instrumentation.
* Experience with method validation, GMP compliance, and SOP creation.
* Proven ability to organize and prioritize work efficiently.
* Strong attention to detail is essential.
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