Quality Control Specialist

3 weeks ago


Saskatoon, Canada ZYUS Life Sciences Full time

**Summary**:
**Quality Control Specialist**

The ZYUS vision is to elevate cannabinoid-based therapeutics as a standard of care and expand the potential of protein-based formulations in pursuit of a transformational impact on patients’ lives around the world.

**ZYUS. Advancing the science of well-being.**

Join us on our mission.

**Main Duties**:
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.
- Lead analytical test method validation and verification protocols.
- Lead equipment qualification protocols.
- Lead QC equipment maintenance and calibration program.
- Lead laboratory deviation investigations and develop investigative protocols.
- Train QC personnel on lab methods and instrumentation.
- Perform QC internal audits.
- Develop and perform test protocols and summarize results.
- Report and participate in the resolution of all deviations.
- Participate in the assignment and execution of CAPA.
- Lead/review Change Controls, Deviations/Investigations, Risk Assessments, assessing proposed changes to validated processes to identify requirements necessary to maintain validated status.
- Follow all established laboratory, regulatory, safety and environmental procedures.
- Author, review and update SOP's as needed; understand and follow complex written procedures.
- Must follow good documentation practices in all aspects and phases of work.
- Provide reports for review in a timely manner.
- Assist in the review and approval of QC data.
- Maintain the safety and orderliness of the lab.
- Material handling and inventory control, including controlled substances.
- Adhere to company policies and site SOP's.

Qualifications:

- The qualifications required for this position include a Bachelor of Science degree in Chemistry or a related field.
- Minimum 3 years of laboratory experience, preferably in a cGMP, GLP setting. Experience with HPCL/UPLC systems is required.

We offer a competitive compensation package that is determined by skill level, education and experience. We thank all the applicants; only those selected for an interview will be contacted.


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