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Quality Assurance Specialist - Pharmaceutical Packaging


Brian Pho


Technical Management

Work city:

Hamilton, ON

Work start:






Quality Specialist - Pharmaceutical Packaging

Location: Hamilton, ON

Salary: $55,000 - $65,000 per annum (Base salary) + Bonus.

We are looking for a Quality Assurance Specialist in Pharmaceutical Packaging.

You will possess:
Education and Experience
 BSc
 certifications an advantage including Quality Auditor, Quality Engineer, Quality Improvement Associate, Six Sigma
 quality inspection, auditing and testing experience, GMP experience in pharma
 experience with implementation of corrective action programs
 product or industry-specific experience
 strong computer skills including Microsoft Office, QA applications and databases
 knowledge of tools, concepts and methodologies of QA
 knowledge of relevant regulatory requirements
Key Competencies
 attention to detail
 communication skills - verbal and written
 data collection, management and analysis
 problem analysis and problem solving
 planning

General Purpose

Responsible for ensuring a product or service meets the established standards of quality including reliability, usability and performance.

Main Job Tasks and Responsibilities
 draft quality assurance policies and procedures
 interpret and implement quality assurance standards
 evaluate adequacy of quality assurance standards
 devise sampling procedures and directions for recording and reporting quality data
 review the implementation and efficiency of quality and inspection systems
 plan, conduct and monitor testing and inspection of materials and products to ensure finished product quality
 document internal audits and other quality assurance activities
 investigate customer complaints and non-conformance issues
 collect and compile statistical quality data
 analyze data to identify areas for improvement in the quality system
 develop, recommend and monitor corrective and preventive actions
 prepare reports to communicate outcomes of quality activities
 identify training needs and organize training interventions to meet quality standards
 coordinate and support on-site audits conducted by external providers
 evaluate audit findings and implement appropriate corrective actions
 monitor risk management activities
 responsible for document management systems
 assure ongoing compliance with quality and industry regulatory requirements

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