columbus lab jobs entry Jobs – 4 Openings This Week

Quality Assurance and Regulatory Affairs Associate - Entry Level
BTNX Inc. —Markham, ON
- $40,000–$45,000 a year
- Full-time
- Master's degree
- Bachelor's
- Quick service & fast food restaurant
- Disability insurance
- Dental care
11d
Manufacturing Technician - Quality
Accuenergy Canada Inc —Toronto, ON
- $43,000–$50,000 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Designated paid holidays
Quick apply
4d
Dental Laboratory Junior Technician
Krest Dental Ceramics —East York, ON
- $40,000–$60,000 a year
- Full-time
- CAD
- Laboratory experience
- English
- Dental care
- Vision care
Quick apply
2d

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Quality Assurance and Regulatory Affairs Associate - Entry Level
BTNX Inc. —Markham, ON
Bachelor’s or master’s degree or equivalent in Regulatory Affairs, Medical Science, Life Science or another relevant field. Recognized Degree in Relevant Field.
$40,000–$45,000 a year
11d
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Quality Assurance and Regulatory Affairs Associate - Entry Level

BTNX Inc.
Markham, ON

Apply Now

Job details

Full-time
11 days ago

Benefits

Extended health care
Disability insurance
Dental care
On-site parking

Skills

Master's degree
Bachelor's
Communication skills

Full job description

Job Title: Quality Assurance and Regulatory Affairs Associate - Entry Level

Department:

Quality Assurance and Regulatory Affairs

Employment Type: Full-time

Location: 722 Rosebank Road, Pickering, Ontario

Company Overview

BTNX Inc. (BTNX) is a leading biotechnology company specializing in rapid, point-of-care diagnostics. As a pioneer in the field, we are dedicated to innovation, research, and the development of advanced in-vitro diagnostic (IVD) tests. Our operations extend across laboratories, clinics, hospitals, and physician offices, with our core business presence in Canada & USA as well as a global presence spanning dozens of countries. Headquartered in Pickering, ON, BTNX offers an exciting opportunity for a motivated individual to join our team.

Job Overview

The Quality Assurance and Regulatory Affairs Associate is responsible for the upkeeping and monitoring of the Quality System, to ensure its effective use and functionality. This position requires the development of an in-depth knowledge of all facets of the company and of the various regulations and quality systems of which BTNX Inc. may be a part. The Quality Assurance and Regulatory Affairs Associate is responsible for all the tasks outlined by the pertinent regulations, which include the ISO13485:2016, US FDA QSR, IVDR, Health Canada MDR.

Job Responsibilities

Ensuring Senior Management is up to date on medical device regulatory requirements, and ensure required changes or updates are implemented
Ensuring all facility and product registrations are current i.e. Health Canada, FDA, CE mark
Assist in preparation of documents and submission for FDA, Health Canada, EU, and other international product registration
Involved in updating and maintaining of BTNX’s ISO 13485 QMS
Involved in Internal audit process and to coordinate external audits
Document Control: Creation, revision, review, approval, and control of documents
Review of complaint files, Nonconformity Documentation forms, and corrective/preventative actions
Risk management as determined in meeting all applicable regulatory requirements
Review and approval of content for Product Labeling
Recalls and medical device reporting
Assist in organization of Management Review meeting(s)

Salary and Benefits

$40,000.00 - $45,000.00 CAD annually - pay commensurate to experience.

Benefits

Dental care
Disability insurance
Extended health care
On-site parking

Schedule:

Monday to Friday

Required Skills/Qualifications

Bachelor’s or master’s degree or equivalent in Regulatory Affairs, Medical Science, Life Science or another relevant field
0 to 2 years of relevant experience (or demonstrated abilities)
Strong Organizational and Multi-Tasking Skills
Recognized Degree in Relevant Field
Regulatory Affairs knowledge (strongly preferred)
Quality Systems knowledge (preferred)
Experience in FDA or Health Canada, and/or European in-vitro diagnostic medical device regulations
Excellent communication skills, including written, oral, and phone

Application

To apply, submit your resume and a cover letter explaining your interest and qualifications for the role to [email protected]. For questions about the application process, please contact [email protected]. We look forward to learning more about how you can contribute to our team.

AI will be used as part of the applicant screening process.

Apply Now

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