Certifying Scientist

**JOB SUMMARY**

Dynacare is currently searching for a Certifying Scientist - Positive to join our Forensic Toxicology team in London, Ontario. This is a permanent, full-time position working 37.5 hours per week. 7am-3pm, 9am-5pm, 10am-6pm on a rotational basis
- Monday - Friday, Tuesday - Saturday on a rotational basis.

**_ Internal job posting closes on August 22, 2023 at 5:00pm(EST). _**

Responsible for approval of screening results for all positive and negative, ensuring calibration, controls and proper procedures are followed and chain of custody is appropriately maintained in accordance with SOP. Review and verify results of GCMS/LCMS. 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.

**KEY RESPONSIBILITIES**
- Review calibration, quality control, emit screening data and validity testing from screening batch
- Review quality control an 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 emit 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 amount 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
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**KNOWLEDGE, EDUCATION AND EXPERIENCE**
- 4 Year Undergraduate Degree or/and Bachelor of Science Degree in Biochemistry or similar area of study
- CSMLS Registration as a practicing Medical Laboratory Technologist in good standing preferred
- Toxicology specific continuing education
- Clinical laboratory experience with experience using toxicology specific laboratory instruments and processes
- 1 to 2 years of related experience required

**SKILLS AND ABILITIES**
- 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

**WORKING CONDITIONS**
- Perform duties in stationary standing/sitting positions
- High visual requirements
- Exposure to bio-hazardous material on a regular basis
- Noise from instrumentation upon occasion
- Some lifting and moving of reagents

**DNA of an Ideal Dynacare Employee**

I make a difference in people’s lives. I am a caring, collaborative team-player who is passionate about quality and continuous improvement.
- Caring - I demonstrate strong empathy and genuine concern for my colleagues, patients and customers.
- Collaborative Team Player - I know I play a key role in helping the Dynacare team achieve success. I am comfortable in a changing environment, and I can easily manage multiple priorities.
- Passion for Quality and Continuous Improvement - I am always looking to learn and solve problems. I am detailed oriented, adaptable and find ways to make things better.

Dynacare has been a “Top Employer” for many years and there is a reason why. We are a great place to work.

If your qualifications and experience fit with this position, we will contact you to learn