Quality Control Technician - Kanata, Canada - Evik Diagnostic Innovations

Evik Diagnostic Innovations

Verified Company

Kanata, Canada

2 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Quality Control Technician

WHO WE ARE:
As part of the team at EVIK Diagnostics Innovations you'll discover meaningful work within the medical device industry. You'll join a rapidly growing company where each day is different, and opportunities are approached with a team effort.

If you'd like to learn more about us and what we do, feel free to check out our website and watch our company video.

Reporting to the Quality Control Manager (presently vacant, will temporarily report to Director of Manufacturing and Production, with 'dotted-line' reporting to Quality Director), performs in-process and final inspections of materials and documentation in manufacturing, inspects incoming material and outgoing product for compliance with requirements, reviews and communicates changes to relevant documentation to assist EVIK Diagnostics in meeting and exceeding customer specifications.

KEY RESPONSIBILITIES

Adheres to current good manufacturing practices and standard operating procedures, to maintain a safe and clean work environment.
Maintain a contaminationfree workspace and wear appropriate PPE when required.
Incoming inspection of raw materials.
Outgoing inspection and testing of finished products to customers.
Maintain accurate batch records and documentation according to the Quality Management System.
Records and inputs data into applicable inspection logs, forms, reports, and databases ensuring accuracy of all recorded information.
Performs batch record review.
Reports and follows up with parts and materials that fail quality inspections and tests.
Perform inprocess visual inspection of freezedried chemical reagent beads and other products to identify nonconforming or damaged products (aka sift and sort).
Perform sample analysis using analytical methods.
Performs measuring instrument verification and calibration per documented procedures
Prepares summaries & trend reports from QC data
Drafts incoming inspection SOPs
Please note this is not a comprehensive list of duties and requirements. Additional responsibilities may be assigned as needed.

SKILLS AND QUALIFICATIONS

College Diploma or relevant experience in the field of Biotechnology.
Knowledge of quality management systems such as ISO9001, ISO13485 or cGMP.
High attention to detail.
Proven English language communication skills both written and oral.
Experience working in a laboratory environment or with medical devices will be considered an asset.
Experience using inspection tools and equipment (e.g., Microscopes, calipers) will be considered an asset. Dedication to production quality and deadlines.
Adaptable to rapidly changing plans and deadlines with a demonstrated resourcefulness and ability to work with a diverse set of tasks and responsibilities.
Ability to perform repetitive tasks.
Ability to work independently and as a member of a small team.
Ability to work in sitting and standing positions and be able to lift up to 20 kg
Good eyesight and hand / eye coordination.
Visual and manual dexterity.
Computer competency (Microsoft Office)