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Grifols

Quality Assurance Specialist

Grifols

Quality Assurance Specialist at Grifols improving healthcare through plasma-derived medicines. Performing daily QA functions like reviews and providing support to production and engineering teams.

Posted 7/2/2026full-timeMontreal • 🇨🇦 CanadaJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Quality Assurance within the biopharmaceutical industry, focusing on quality systems, regulatory compliance, and data integrity. Proficient in conducting investigations, managing deviations, and implementing CAPA processes.

Highest-signal resume keywords
Quality Assurance ExperienceQuality Systems ExpertiseRoot Cause AnalysisCAPA ManagementRegulatory Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Change ControlDeviations ManagementInvestigationsRisk AssessmentsQuality Metrics Development
Soft Skills
JudgmentTechnical CompetenceTeam CollaborationIndependent Work
Industry Keywords
Biopharmaceutical IndustryPharmaceutical ManufacturingData IntegrityTraceabilityQuality Control

About the role

Key responsibilities & impact
  • Perform the following daily functions, including but not limited to: review of deviations, investigations, and CAPA
  • Ensure the integrity and traceability of all data generated and reported
  • Provide support to other departments such as Production, Quality Control, Validation, and Engineering
  • Develop and report quality metrics for deviations and other systems, as assigned
  • Assume additional responsibilities under the quality system program, as trained and assigned

Requirements

What you’ll need
  • Bachelor's degree in Science required (preferably in Microbiology, Chemistry, or Biology)
  • Minimum 2–3 years of Quality Assurance experience in the biopharmaceutical or pharmaceutical manufacturing industry
  • Specialist-level expertise with advanced knowledge of quality systems (change control, deviations, investigations, root cause analysis, CAPA, and risk assessments)
  • Demonstrated judgment, technical competence, and subject-matter knowledge essential to the role
  • Able to apply, follow, and rigorously maintain rules, regulatory requirements, procedures, and processes
  • Able to work independently and as part of a team

Benefits

Comp & perks
  • Proficient computer skills with MS Office and Adobe Acrobat
  • Strong organizational skills, with attention to detail and ability to meet deadlines