QA Specialist

Posted 07 January 2022
Job type Limited
DisciplineLife Sciences

Job description

For its Medical Devices partner, Kelly Life Sciences is looking for:

QA Specialist
(Temporary mission - min 6 months)

Your mission:

  • You will be reporting to Regulatory Affairs and Quality Assurance Manager
  • You will ensure conformity of good manufacturing practices and QMS

Your responsibilities:

  • Guarantee the application of applicable standards and regulations (i.e. ISO13485, MDSAP, 21CFR part 820)
  • Support and manage quality events (incident report, non-conformances)
  • Contribute to quality assurance documentation (release documents, records)
  • Participate to training steps related to your scope of activities
  • Define corrections, corrective and preventive actions to prevent reoccurrence of events
  • Participate to continuous improvement
  • Support QA Team during audits & inspections
  • Ensure back up of other QA Team members when applicable
  • Support and promote the diffusion of a high-quality mindset in the company

Your profile:

  • Scientific education such as biological, biochemist, medical devices, quality assurance or equivalent
  • Experience in Medical Devices Quality Management Systems (21 CFR part 820 & ISO13485)
  • Knowledge of GMP environment
  • At ease with Microsoft Office and usual software tools
  • Fluent in English & French

Your contact at Kelly:
Anaïs Mieszczak
Consultante Professional Staffing
Kelly Life Sciences