Quality Assurance Auditor

Liberty Staffing; Cambridge; On-site; CAD 50,000 - 70,000; Full time

Job summary

A staffing agency in Cambridge, Canada, is seeking a Quality Assurance professional for a 12-month contract covering maternity leave. The role involves ensuring compliance with regulatory standards, improving systems for product quality, and working with third-party manufacturers. Candidates must have a degree in a science-related field and relevant pharmaceutical experience. Key skills include critical thinking and attention to detail.

Qualifications

• Pharmaceutical experience in a manufacturing environment is essential.
• Degree in a science related field required.
• Strong critical thinking and attention to detail are needed.

Responsibilities

• Ensure Quality Standards are met for material released in the Canadian Market.
• Track third party performance and propose improvement actions.
• Maintain appropriate Health Canada and GMP records.

Skills

Pharmaceutical Experience

Critical Thinking

Attention to detail

Education

Degree in a science related field

Job description

Overview

This position is a contract position covering a 12 month Maternity Leave. This position supports products manufactured and/or distributed in the Canadian market, continuously improving key systems and processes to ensure product quality, regulatory compliance and efficiency. This position works directly with Third Party Manufacturers, warehouse facilities as well as directly with the client.

Responsibilities

• Quality Assurance
  • Ensure Quality Standards are met for material released in the Canadian Market and transactions are processed in a timely manner.
  • Ensure all supplier qualification activities satisfy all regulatory requirements and audit reviews.
  • Change Control Review
  • Deviation review (as applicable)
  • Complaint investigation and maintenance
• Performance
  • Propose improvement actions and report regularly on implementation progress.
  • Track third party performance and report regularly to local and corporate departments.
  • Focus on standardizing all operations in the interest of improving the operating compliance and performance standards.
• Regulatory Compliance
  • Maintain appropriate Health Canada and GMP records for HC Inspectorate.
  • Provide required documentation to support regulatory body requests (incomplete letters, review questions and investigation progress).

Qualifications

• Pharmaceutical Experience in a manufacturing environment
• Must hold a Degree in a science related field
• Critical Thinking
• Attention to detail
• Accommodations are available upon request for all individuals with disabilities taking part in the recruitment and selection process.