Quality Engineer – Medical Devices & Continuous Improvement

Abilia AB

Solna kommun

On-site

SEK 520,000 - 700,000

Full time

14 days+

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Job summary

Abilia AB in Solna, Stockholm, is seeking a Quality Engineer | QA Specialist to ensure product quality across the supply chain and manufacturing. You will collaborate with Development, Operations, Manufacturing, Supply Chain and Regulatory Affairs, as well as external suppliers.

The role focuses on continuous improvement, risk identification, CAPA coordination, audits, and data analysis. You will report to the Quality Manager and contribute to strengthening quality processes within the

Qualifications

  • Bachelor’s degree in Engineering, Life Science or equivalent technical discipline.
  • 2–5 years in Quality Engineering/QA in regulated settings.
  • Knowledge of ISO 9001 and/or ISO 13485.
  • Experience with Q-tools: FMEA, RCA, 8D, CAPA or Six Sigma.
  • Strong analytical and problem-solving abilities.
  • Proficient Swedish and English communication.

Responsibilities

  • Support quality systems and supplier quality across the supply chain.
  • Perform internal quality audits according to ISO 13485.
  • Lead supplier audits and address findings.
  • Drive continuous improvement initiatives and CAPA processes.
  • Investigate quality issues and perform root-cause analyses.
  • Analyze quality metrics and monitor defect trends.

Skills

Quality mindset
Analytical thinking
Communication skills
Independent working
Collaboration

Education

Bachelor's degree in Engineering/Life Science or related

Tools

FMEA
Root Cause Analysis
8D
CAPA
Six Sigma

Job description

Abilia AB in Solna, Stockholm, is seeking a Quality Engineer | QA Specialist to ensure product quality across the supply chain and manufacturing. You will collaborate with Development, Operations, Manufacturing, Supply Chain and Regulatory Affairs, as well as external suppliers.

The role focuses on continuous improvement, risk identification, CAPA coordination, audits, and data analysis. You will report to the Quality Manager and contribute to strengthening quality processes within the

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