Prollenium Medical Technologies Inc.

Quality Assurance Associate

Prollenium Medical Technologies Inc.

contract

Posted on:

Location Type: Hybrid

Location: Richmond HillCanada

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About the role

  • Provide prepared documentation in support of audits and inspections from regulatory agencies ie. Health Canada, US FDA, Brazilian, European, UK, Australia, Japan
  • Assist in requesting Quality Metrics from PMT Depts for discussion during Management Review
  • Support the validation program by issuing validation report numbers, change control forms and obsolescence of older versions within the QMS
  • Edit and save SOPs as needed
  • Assist in coordinating PMT’s company-wide training program
  • Accession new customer complaints, collect information, prepare reports, submit within required timeframes
  • Develop and maintain documentation to ensure compliance for critical and non-critical suppliers (certificates, contracts/agreements, supplier audits, and corrective actions)
  • Maintain retrievable records (paper and/or electronic) of lower level inventory items
  • Fill paperwork as per GMP requirements
  • Participate in releasing lower-level inventory items using PMT’s ERP system
  • Participate in statutorily required meetings related to company health and safety policies

Requirements

  • 1 - 3 or more years of work experience in a Quality Assurance function in an ISO 9001, 13485 or 17025 environments
  • University degree in the science (chemistry, biology, pharmacy or similar)
  • Excellent written and oral communication skills
Benefits
  • Competitive compensation
  • Health insurance
  • Professional development opportunities
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
Quality AssuranceISO 9001ISO 13485ISO 17025GMPdocumentationvalidationchange controlsupplier auditsreport preparation
Soft Skills
communicationorganizationalattention to detailproblem-solvingteam collaboration