Senior Specialist Capa

Stryker Corporation

Montbonnot-Saint-Martin, France
Competitive salary; performance-based bonuses; hea...
Hybrid
Nc/capa process management
Root cause analysis execution
Regulatory compliance assurance
Stryker Corporation is seeking a Senior Specialist CAPA to oversee non-conformities and corrective/preventive actions in their Montbonnot-Saint-Martin facility. The role requires experience in regulatory environments, particularly within the medical device sector, and offers a hybrid working model with a focus on career development and employee recognition

Job Summary

  • The role involves leading the Non-Conformity and Corrective/Preventive Action (NC/CAPA) process from initiation to closure while ensuring regulatory compliance.
  • Candidates will conduct root cause analyses, evaluate corrective actions, and drive continuous improvement initiatives within a quality-focused environment.
  • Stryker offers a flat hierarchy structure that encourages employee initiative, along with competitive compensation and comprehensive benefits packages.

Matching Summary

Match Score: 85

Stryker Corporation is seeking a Senior Specialist CAPA to oversee non-conformities and corrective/preventive actions in their Montbonnot-Saint-Martin facility. The role requires experience in regulatory environments, particularly within the medical device sector, and offers a hybrid working model with a focus on career development and employee recognition.

Salary

Competitive salary; Performance-based bonuses; Health insurance, retirement plans, wellness programs

Skills & Requirements

Must-have

  • NC/CAPA process management
  • Root cause analysis execution
  • Regulatory compliance assurance
  • Internal audit participation
  • Trend analysis for improvement

Nice-to-have

  • International team collaboration
  • Cross-functional influence skills
  • Continuous improvement mindset
  • Project management capabilities
  • Training and mentoring abilities

Key Requirements

  • Minimum 2 years NC/CAPA experience
  • Experience in regulated medical device sector
  • Knowledge of ISO 13485 and MDSAP standards
  • Bachelor's degree or equivalent (Bac+3)
  • Professional English proficiency required

Work Rights

Not specified

Tailored Resume

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