Certifying Scientist - Positive

Dynacare • London, ON

36d • $32 - $35 • Onsite

About The Position

Life is precious and every moment matters. Dynacare is helping Canadians achieve a healthy future with care and wellness solutions that are convenient, understandable, and accessible. When you join our team, every day is an opportunity to get better and be inspired. It’s an environment where you can grow your career in any direction you choose. We’re evolving our technology and optimizing our processes, so you can do your best work, make a meaningful impact, and thrive.
As a Certifying Scientist - Positive, you will be responsible for approval of results for all positive and negative tests, ensuring calibration, controls, and proper procedures are followed and chain of custody is appropriately maintained in accordance with SOP. Review and verify results of gas and liquid chromatography/mass spectrometry (GCMS and LC/MS/MS). Responsible for the performance and release of various laboratory tests following set procedures. Ensure all quality control checks and standards are run as required. Participate in all quality assurance programs and adhere to company and external regulatory bodies guidelines. Perform routine maintenance of laboratory equipment as appropriate.

Requirements

• 4 Year Undergraduate Degree or/and Bachelor of Science Degree in Biochemistry or similar area of study
• Clinical laboratory experience with experience using toxicology specific laboratory instruments and processes
• 1 to 2 years of related experience required
• Demonstrated ability to correctly identify samples and ensure specimen testing requirements are completed following established procedures using manual and automated processes
• Ability to identify, observe and report all malfunctions with clinical instruments
• Demonstrated analytical and problem-solving ability
• Demonstrated success at building relationships and collaborating with a network of internal colleagues and subject matter experts
• Ability to work independently and effectively with minimal supervision focusing on results
• Ability to effectively prioritize and execute tasks in a high-pressure environment

Nice To Haves

• CSMLS Registration as a practicing Medical Laboratory Technologist in good standing preferred
• Toxicology specific continuing education

Responsibilities

• Handling controlled documents (e.g., chain of custody)
• Review calibration, quality control, EIA screening data and validity testing from screening batch
• Review quality control and patient values for acceptability of results
• Check chromatography for acceptability
• Verify data and information is correct on all documents and correct errors as necessary
• Review chain of custody and custody and controls forms
• Interpret data, enter, and approve results
• Certify adulterated, substituted, and invalid results
• Review and certify EIA screening data and validity testing data
• Ensure correctness of all documentation, information, and data
• Ensure sample identification is correct and specimen requirements are met according to established procedures
• Responsible for the follow-up on missing samples, documentation, and results in the respective department
• Perform patient’s sample testing and measurement using a variety of manual and automated procedures
• Record, interpret and/or approve test results according to established procedures in a timely manner
• Ensure that all abnormal Stat and critical results are handled as outlined in the department guidelines
• Sign-off on reports as required
• Consult with the department supervisor to assist with non-routine problems and concerns
• Ensure all inquiries and problems are handled in a courteous professional manner
• Ensure that Quality Control and Quality Assurance are run according to department policies and procedures
• Participate in external proficiency testing programs and inspections
• Follow guidelines as required by external regulatory bodies
• Responsible to follow all relevant pre and/or post analytical QA protocols as described in the company QA manual
• Observe and report all malfunctions with equipment and record all corrective action(s) taken
• Follow manufactures’ guidelines for the operation, maintenance, and minor troubleshooting and maintain all logbooks for routine equipment maintenance
• Participate in training staff as outlined in department procedure manuals
• Ensure adequate number of supplies are on hand and that validated in date reagents and testing kits will be used
• Ensure maintenance of inventory records
• Maintain confidentiality of appropriate documentation

Benefits

• Access a health and wellness benefits program that supports you and your loved ones
• Grow and thrive with a dynamic, successful company through internal mobility opportunities
• Invest in your future through RRSP match benefits and an employee stock purchase program

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level