Senior Quality Engineer

☞ Integra LifeSciences

View: 240

Update day: 21-03-2024

Location: Le Locle Neuchâtel NE

Category: Quality Assurance / Quality Control

Industry: Medical Equipment Manufacturing

Position: Mid-Senior level

Job type: Full-time

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Job content

Responsibilities

  • Quality support for production (various production lines) and for various projects
  • Plan, coordinate and direct the quality aspects of process validation
  • Write validation documentation (protocols, reports, process specifications, work instructions, pFMEA, master validation plan)
  • Non-conformance management (initiation / evaluation / disposition on the batches / investigation)
  • CAPA management
  • Review and approve changes to documentation and processes
  • Provide projects updates and presentations
  • Quality control technical support
  • Participation in development and updating of procedures and other quality documents
  • Participation in validations of new processes (Processes, products, methods & software)
  • Validation of different integrated processes of Integra LifeSciences & Codman Neurosurgery
  • Apply and enforce GMP

Qualifications

  • Minimum of 4 years’ experience in Quality Engineering area (Medical device or pharma industry experience highly preferable)
  • Engineering degree or equivalent
  • Knowledge in statistic (capability, gage RR, Anova test, control chart)
  • Quality knowledge in the medical industry
  • Organized and methodical
  • Outstanding communication skills with outgoing and proactive attitude
  • Solid organizational skills
  • Team spirit
  • Fluent in French and English
  • Ability to work with cross functional team (R&D, RA, manufacturing engineering, planning, production)
  • Proactive, rigorous, autonomous

In an effort to minimize the spread of the coronavirus and to protect our employees, all new hires in the US and Puerto Rico will need to be fully vaccinated for COVID-19 in order to be considered for employment with Integra LifeSciences, unless eligible for an accommodation as provided by law.

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Deadline: 05-05-2024

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