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Qvella Corporation: Production Qc Technician

Qvella Corporation

This is a Full-time position in Metropolitan Area Apt, ON posted July 9, 2021.

An exciting opportunity for Production Quality Control Technician, this is a permanent opportunity with Qvella Corporation located in Richmond Hill, Ontario.Nature and Scope of Work:Responsible for QC functions and activities related to cartridge and reagent production line.

Maintain production quality control standards by approving incoming materials, in-process products, and finished products in accordance with established SOPs/GMP/ISO standards.Essential Duties and Responsibilities:To perform this job successfully, an individual must be able to perform each essential duty satisfactorily:Approve incoming materials, in-process products and finished products by confirming specifications, conducting visual inspection and performing measurements/tests; rejecting unacceptable materials; communicating findings to production supervisor.Maintain effectiveness of QC activities and documentations.

Manage materials inventory to support routine QC testing requirements.

Document inspection results by completing reports/logs and inputting data into QC databaseAnalyze testing data and report findings and conclusions through written and oral presentations.Investigate non-conforming materials/products and provide feedback, recommendation/solution for corrective/preventive actionsEnsure testing/measurement equipment operational by following maintenance and calibration schedules.Maintain the integrity of QC lab and cleanroom including cleaning work stations, organizing tools and fridges/freezersWork with production team and QA to improve yield and reduce production wasteAssist production and process improvement efforts as requiredOther duties as assignedQualifications and Requirements:2 3 years hands-on quality control experience in medical device production environment.Good knowledge of the principles of general chemistry and related natural sciences.Working familiarity with mechanical drawings and diagramsHigh level of proficiency in general lab equipment and testing tools (e.G.

caliper, pipettor, vortex mixer, scales, etc.)Ability to work meticulously and independently with minimal supervisionUnderstanding of bioscience quality/safety requirements and regulations.Strong test, measurement problem-solving and analytical skillsGood written and verbal communication skills in English.Good understanding of GMP and ISO quality system methodology.Flexibility, strong team approach and capable of multi-tasking, strong sense of individual responsibilityGood MS-Office skillsEducation:University degree or equivalent in science, engineering or other related fields.What are you waiting for?

Apply Now!Qvella is an equal opportunity employer.

We are committed to a diverse and inclusive workplace for all.

If you are selected to participate in the recruitment process, please inform us of any accommodations you may require.

Qvella will work with you in an effort to ensure that you are able to fully participate in the process.

All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.Must be legally eligible to work in Canada at the location(s) specified above and, where applicable, must have a valid work permit or study permit that allows the candidate to fulfill the requirements of the role.We thank all interested applicants; however, only those selected for an interview will be contacted.Powered by JazzHRaTOfXi4thL