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Quality Assurance Associate

  • Mississauga, ON, Canada

This is a full time hybrid role with a salary range of $62,000 to $70,000 per year. · Full-time

This opening has closed.

The original listing is kept below for reference.

Job details

Pay
This is a full time hybrid role with a salary range of $62,000 to $70,000 per year.
Job type
Full-time
Closing date
Posting language
English
Posted

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Original job description

Archived listing. The details below describe a past opening.

About the role

Mint Pharmaceuticals is hiring a Quality Assurance Associate to join its quality team in Mississauga, Ontario. This is a full time hybrid role with a salary range of $62,000 to $70,000 per year.

You will own the preliminary review of documents for product release, review executed batch records, and track third party testing and stability data. You will work closely with warehouse staff, contract fabricators and foreign sites to ensure every product released to market is fully compliant with current Health Canada GMPs.

For a candidate with exceptional depth, there is scope for this position to be set at Senior QA Associate level.

What you will do

  • Conduct the preliminary review of documents for product release, including executed batch documentation.
  • Coordinate finished product testing and review the quality documentation required to release finished products to market.
  • Ensure SOPs across product importation, distribution, testing, warehousing and quality assurance remain compliant with current Health Canada GMPs.
  • Assist with and execute product recalls as required by company policy and Health Canada.
  • Approve products intended for destruction.
  • Perform temperature downloads, and define and execute temperature mapping where applicable.
  • Coordinate with warehouse staff on incoming product inspection and label review.
  • Maintain retain sample inventory, including the annual physical inventory of retain samples.
  • Communicate promptly on documentation and release issues, including delays from contract fabricators and deviation investigations.
  • Collect and review technical records from foreign sites, such as method and process validation protocols and reports.
  • Track stability for commercial and submission lots and ensure data supporting shelf life is properly filed.
  • Interface with third party and foreign site organizations on GMP matters to meet Canadian GMP requirements.

What we are looking for

  • Minimum three years of quality assurance experience in a Canadian generic pharmaceutical environment.
  • Working knowledge of Canadian GMPs and relevant Health Canada policies and guidances.
  • Bachelor of Science in a science related discipline. Postgraduate training in Pharmaceutical Quality Studies is an asset.
  • Hands on experience reviewing and dispositioning executed batch records.
  • Works independently with minimal supervision and is decisive by nature.
  • Meticulous, detail oriented, and highly organized across multiple concurrent projects.
  • Strong problem solving and analytical ability, with a track record of issue resolution and process improvement.
  • Excellent written and verbal communication skills.
  • Proficient in Microsoft Excel, Word and PowerPoint.

Applications are managed by Rossi Recruitment on behalf of Mint Pharmaceuticals.

More about this job

Responsibilities

Review product release documentation and executed batch records, coordinate finished product testing, and ensure products and procedures comply with current Health Canada GMPs. Manage recalls, temperature monitoring, warehouse inspections, retain samples, stability records, and technical documentation while coordinating with contract fabricators and foreign sites.

Requirements

Requires at least three years of quality assurance experience in a Canadian generic pharmaceutical environment, working knowledge of Canadian GMPs and Health Canada guidance, and a Bachelor of Science in a science-related discipline. Candidates should have hands-on batch record review and disposition experience, strong organizational, analytical, and communication skills, and proficiency in Microsoft Office; postgraduate training in Pharmaceutical Quality Studies is an asset.

Skills

  • Quality Assurance
  • Canadian GMP Compliance
  • Executed Batch Record Review
  • Product Release
  • Finished Product Testing
  • SOP Compliance
  • Product Recall Execution
  • Temperature Mapping
  • Incoming Product Inspection
  • Label Review
  • Retain Sample Inventory
  • Stability Data Tracking
  • Technical Record Review
  • Deviation Investigation
  • Problem Solving
  • Microsoft Excel

Visa sponsorship

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Categories

  • Healthcare
  • Manufacturing
  • Science & Research

Keywords

  • Quality Assurance
  • Pharmaceutical Manufacturing
  • Generic Pharmaceuticals
  • Canadian GMPs
  • Health Canada
  • Product Release
  • Batch Records
  • Finished Product Testing
  • Standard Operating Procedures
  • Product Recalls
  • Temperature Monitoring
  • Temperature Mapping
  • Warehouse Inspection
  • Label Review
  • Retain Samples
  • Stability Data
  • Technical Records
  • Method Validation
  • Process Validation
  • Deviation Investigations
  • Contract Fabricators
  • Product Importation
  • Product Distribution
  • Microsoft Excel
  • Microsoft Word
  • Microsoft PowerPoint

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