Quality Control Technician

Summary

Quality Control Technician – 12 Month Period

ZYUS (TSXV:ZYUS) Canadian-based life sciences company focused on the global development and commercialization of regulated cannabinoid-based pharmaceutical drug product candidates. Through clinical research, ZYUS is committed to furthering the understanding of cannabinoids with the clinical development of its pharmaceutical drug product candidates and intellectual property activities to protect its novel formulations. Additionally, ZYUS is dedicated to delivering high quality, cGMP/EU GMP-compliant cannabinoid products to patients through the exempt global medical market.

The ZYUS vision is to reimagine the potential of pain therapeutics by pursuing regulatory approval of cannabinoid formulations and elevating cannabinoids as a standard of care in pursuit of transformational impact on patients’ lives.

ZYUS. Advancing the science of well-being.

Role Overview:

The Quality Control (QC) Technician will be responsible for performing routine sampling and testing for product, raw material, and packaging, and equipment qualification in conformance with current Good Laboratory Practices (cGLP). They will conduct material sampling, maintain sample chain of custody, and report results accurately.

Your Contribution:

The following is a general description of duties that are done regularly in this role. Please note that employees will be asked to perform duties outside of the following to assist in other Company-related activities as required.

• Conducting routine testing for product, raw material, and packaging.
• Qualifying equipment in conformance with cGLP standards.
• Maintaining sample chain of custody and reporting results accurately.
• Performing material sampling and ensuring compliance with procedures.
• Performing testing for analytical method development and validation.
• Following established laboratory, regulatory, safety, and environmental procedures.
• Adhering to cGLP standards and the company's Quality Policies and site Standard Operating Procedures (SOPs).
• Providing reports in a timely manner.
• Collaborating with other lab personnel on projects.
• Maintaining lab safety and orderliness.
• Managing material and inventory control, including controlled substances.
• Reporting and participating in resolving deviations and implementing CAPA.

Qualifications:

• Post secondary education in a relevant scientific field.
• Previous experience in a quality control or laboratory environment preferred.
• Experience with analytical instruments such as HPLC, UPLC, UV, etc.
• Familiarity with regulatory requirements and quality standards (e.g., cGLP, cGMP).
• Strong attention to detail and accuracy in record-keeping.
• Excellent communication and teamwork skills.
• Ability to work independently and collaboratively in a fast-paced environment.

Skills, Knowledge, and Abilities:

• Excellent written and verbal communication skills.
• Excellent organizational and analytical skills with a high attention to detail.
• Proficient in utilizing Microsoft Office applications.

Must have the ability to maintain integrity and honesty at all times

How to Apply:

Send a copy of your resume to [email protected].

We thank all applicants for their interest. Only those selected for the next stage will be contacted.

• Please note that this is a 12-month full time, fixed term contract with the possibility of extension.