Chatham Kent, On Quality assurance associate Jobs – 2 Openings This Week

Senior Quality Associate
Decibel Cannabis Company —Chatham-Kent, ON
- $65,000–$75,000 a year
- Weekends as needed
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Quick apply
Bilingual Associate Program Manager
BioScript Solutions —Canada
- Remote
- Bilingual
- English
- Project management
Quick apply

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Senior Quality Associate

Decibel Cannabis Company -
Chatham-Kent, ON

Quick apply

Job details

Full-time
$65,000–$75,000 a year

Qualifications

Microsoft Word
Microsoft Excel
Microsoft Outlook
Post-secondary education
Microsoft Office
Quality assurance
Chemistry
Manufacturing
Communication skills

Full job description

Senior Quality Associate
Location: Chatham, ON
Company: Decibel Cannabis Company / AgMedica Bioscience Inc.

About Us

Decibel Cannabis Company is a consumer-focused cannabis company with a portfolio of premium brands including General Admission, Qwest, and Vox. AgMedica Bioscience Inc., a division of Decibel, operates a GMP-certified cannabis processing facility in Chatham, Ontario, supporting both domestic and international markets.

We are committed to quality, compliance, and continuous improvement in a highly regulated environment.

Position Overview

This is a newly created position within the organization.

Reporting to the QA Supervisor, the Senior Quality Associate plays a key role in supporting and maintaining Quality Assurance systems in compliance with GPP, GACP, and GMP requirements. This role also acts as the Alternate QA Person (AQAP), providing oversight and guidance across departments to ensure regulatory compliance and product quality.

Key Responsibilities

Act as AQAP and support the QA Supervisor in daily quality oversight
Provide guidance and mentorship to Quality staff and cross-functional teams
Maintain and continuously improve quality systems, including SOPs, Work Instructions, and records
Manage supplier quality and ensure compliance of raw materials
Maintain receiving specifications and inspections within internal systems
Support equipment validation and lifecycle activities (DQ/IQ/OQ/PQ)
Conduct internal audits, investigations, root cause analysis, and CAPA implementation
Review and support approval of Batch Production Records (BPRs)
Support environmental monitoring, sanitation validation, and pest control programs
Assist with sampling, testing, and product release activities
Support regulatory inspections and third-party audits
Prepare and maintain quality reports (monthly, quarterly, annually)
Perform other duties as required

Qualifications

Post-secondary education in Chemistry, Biology, Pharmacy, or a related field
3+ years of experience in a Quality Assurance role (pharmaceutical or regulated industry preferred)
Strong knowledge of Good Manufacturing Practices (GMP)
Experience with HACCP and Preventative Control Plans (PCPs) is an asset
Experience with validation/qualification activities is an asset
Previous experience with a Licensed Producer (LP) is considered an asset
Strong technical skills, including Microsoft Office (Excel, Word, Outlook)
Strong attention to detail, organization, and communication skills

Working Conditions

GMP manufacturing environment with required PPE (gowning, mask, gloves, etc.)
Exposure to moderate noise, strong odours, and variable temperatures
Physical requirements may include lifting up to 25 kg, standing for extended periods, and performing repetitive tasks
May require occasional evening or weekend work based on operational needs

Why Join Us?

Work in a highly regulated, GMP-compliant environment
Be part of a growing and innovative cannabis company
Opportunities for professional growth and cross-functional collaboration
Competitive compensation and benefits

Applicants must be 19 years of age or older and able to successfully complete a background check.

7:00 AM - 3:30 PM

Quick apply

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