QC Associate at Assist My Day
Etobicoke, ON, Canada -
Full Time


Start Date

Immediate

Expiry Date

04 Sep, 25

Salary

18.0

Posted On

26 Jul, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Outlook, Excel, Microsoft Word

Industry

Pharmaceuticals

Description

JOB SUMMARY

We are seeking a detail-oriented Quality Control Associate to join our team. In this role, you will be responsible for ensuring that our products meet the highest quality standards through rigorous inspection and testing processes.
Reporting to the Quality Control Manager, the Quality Control Associate is responsible for the administration of QC functions as they relate to Raw Material dispensing, product sampling and inspection of the raw materials, packaging materials, finished goods, and in-process goods to achieve customer product specifications as well as results analysis, documentation and general administrative duties

REQUIREMENTS

  • Must have at least 2 years of nutraceutical / natural health product experience
  • Strong analytical capabilities in chemical and/or microbiological environment
  • Interest in food/natural health products/pharmaceuticals is an advantage.
  • Basic proficiency in Microsoft Word, Excel, Outlook
  • Motivated, positive attitude and an attention to detail necessary
    Job Type: Full-time
    Pay: $18.00-$20.00 per hour
    Expected hours: 40 per week
    Work Location: In person
    Application deadline: 2025-08-05
    Expected start date: 2025-08-1
Responsibilities
  • Follow written procedures for dispensing, sampling, inspecting and approval of raw materials, in-process, finished product and packaging materials.
  • Perform analytical testing
  • Monitoring and enforcing Good Manufacturing Practices.
  • Monitor environmental controls.
  • Maintenance and calibration of equipment.
  • Help in monitoring the facility, trained personnel and equipment are up to GMP standards.
  • Provide support to the QA/QC Team and perform other related duties as required.
  • Interpret test results of all products to approve or reject materials and goods based on established specifications.
  • Enforce Good Document Practices and ensure all in-process records are maintained.
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