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Quality Assurance Specialist at Biopharmaceutical
Job in
Kingston, Ontario, A7K, Canada
Listed on 2026-07-16
Listing for:
Tandem Project Management Ltd.
Full Time
position Listed on 2026-07-16
Job specializations:
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Production QC/QA, Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Job Description & How to Apply Below
Join a leading biopharmaceutical company in Waterford as a Quality Assurance Specialist. Ensure compliance with cGMP standards through effective audit processes and documentation review.
As part of the Quality Assurance team, you will be instrumental in ensuring products are produced, stored, and packaged in accordance with strict cGMP guidelines.
Your role includes developing GMP training, conducting audits, and actively participating in quality initiatives. Bringing your attention to detail and interpersonal skills, you'll address quality system issues and contribute to continuous improvement efforts.
Key Responsibilities:
• Ensure adherence to cGMP in product manufacturing and storage
• Develop and deliver GMP training packages
• Review procedures and batch documentation
• Conduct audits across all departments
• Support investigation of product deviations
Requirements:
• Degree in science or related field preferred
• Minimum 2 years’ experience in QA role
• Knowledgeable in GMP environments
• Strong attention to detail and accuracy
• Good presentation and interpersonal skills
Your expertise in quality assurance and commitment to cGMP standards make you a valuable asset to our Waterford team.
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