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QA Validation & Engineering
QA Validation & EngineeringResolute Workforce Solutions • Richmond Hill, Canada
QA Validation & Engineering

QA Validation & Engineering

Resolute Workforce Solutions • Richmond Hill, Canada
30+ days ago
Job type
  • Full-time
Job description
Resolute Workforce Solutions (Staff augmentation subsidiary of Brevitas Consulting Inc.) is dedicated to helping organizations achieve tangible results and lasting improvements via successful project delivery, continuous process improvement, and effective management of change. Our expertise is in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Project Management.
We are looking for a highly motivated and energetic individual to join our team as a QA Validation & Engineering in Richmond Hill, ON (On-site).
Responsibilities:
  • Review Validation Master Plans, validation strategies, and related documentation to ensure compliance with regulatory and GMP requirements.
  • Act as QA reviewer/approver for validation protocols, reports, commissioning documents, SATs, FATs, qualification activities, change controls, preventive maintenance, and calibration records.
  • Support process validation, equipment and facility qualification, cleaning validation, and technical operations by providing guidance and troubleshooting validation issues.
  • Perform technical assessments and review change controls using quality management systems (, TrackWise).
  • Review and approve investigations, deviations, and corrective/preventive actions (CAPAs) related to validation activities.
  • Participate in cross-functional teams (, product launches, change control boards) and periodic reviews of maintenance and calibration trends.
  • Ensure manufacturing and packaging processes remain in a validated state and comply with GMP and internal quality procedures.
  • Follow company policies related to quality, safety, compliance, and ethics, and perform other duties as assigned.
Qualifications:
  • Bachelor’s degree ( / in a related field or equivalent.
  • 5+ years of pharmaceutical manufacturing experience, including at least 4 years in a validation role.
  • Experience in liquid dosage manufacturing with knowledge of TPD, FDA, EU, and other validation regulatory guidelines.
  • Strong understanding of validation concepts and experience using statistical tools for process capability and control.
  • Proficiency with SAP, TrackWise, and Microsoft Office tools.
  • Strong organizational, project management, problem-solving, and troubleshooting skills.
  • Ability to analyze processes, recommend improvements, and work independently with minimal supervision.
  • Salary: CAD $100,000 – $130,000 (depending on experience).
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QA Validation & Engineering • Richmond Hill, Canada

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