S

Stryker

Manufactures orthopedic and surgical medical devices

Superviseur Contrôle Qualité

Inspection & TestConfirmed live in the last 24 hours
Full-timeGrenoble, France

About the Job

Requirements

  • A minimum Bac+2 qualification in a technical field focused on mechanics, metrology, or quality is required.
  • At least 4 years of experience in a regulated or demanding industrial environment, such as medical devices, automotive, or aerospace, is required.
  • At least 3 years of team-management experience in a production or quality-control environment is required.
  • Knowledge of ISO 13485 and 21 CFR Part 820 is required.
  • Experience with quality and problem-solving analysis tools, including 5M, 8D, FMEA, and SPC, is required.
  • Proficiency with office applications, including Excel, Word, PowerPoint, and Outlook, is required.
  • Professional-level spoken and written English is required.
  • A Bac+5 qualification in engineering, quality, or an associated technical discipline is desirable.
  • Previous experience in industrial engineering, continuous improvement, or industrialization is desirable.
  • Experience with an ERP, a production-management system, and quality software for document management, nonconformities, and CAPA is desirable.
  • Proficiency with statistical software such as Minitab is desirable.

Responsibilities

  • Lead incoming and final quality-control activities to achieve quality, delivery, and performance objectives.
  • Organize resources and workflows to ensure operational continuity and achieve sector results.
  • Monitor performance indicators, analyze deviations, and implement necessary corrective actions.
  • Supervise, develop, and support a quality-control team, including management of objectives, training, and cross-skilling.
  • Contribute to recruitment and ensure the onboarding and skills development of new employees.
  • Ensure compliance with quality requirements, associated documentation, and continuous-improvement standards.
  • Lead or contribute to quality investigations, corrective and preventive actions, and process-improvement projects.
  • Ensure compliance with health, safety, and environmental rules, and participate in internal and external audits and regulatory inspections.
  • Collaborate across production, engineering, quality, and support-function teams.

About the Company

Stryker

Manufactures orthopedic and surgical medical devices

Stryker makes medical devices for hospitals, surgical centers and emergency responders, spanning joint implants, surgical instruments and patient transport equipment. Its Mako platform assists surgeons with joint replacement, while its neurotechnology products support brain and spine procedures and stroke treatment. Clinicians use its equipment during surgery and emergency care, and the company earns money by selling implants, disposable products and capital equipment through direct sales teams and distributors. The business also supplies training and technical support for healthcare providers using its devices. Stryker was founded in 1941 and is headquartered in Portage, Michigan.

Company size
10,001+
Company stage
IPO
Headquarters
Portage, MI
Founded
1941

Recently Posted Jobs

Explore more opportunities at Stryker

See more jobs