Senior Quality Engineer

☞ Integra LifeSciences

View: 199

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

Loading ...

Job content

Integra LifeSciences is a global leader in regenerative technologies and neurosurgical solutions dedicated to limiting uncertainty for clinicians, so they can focus on providing the best patient care.Founded in 1989, Integra develops, manufactures, sells and supplies best-in-class products to regenerate tissue, remove brain tumors, prevent infection and much more. And over the last three decades, we’ve evolved into one of the world’s leading global medical technology companies with more than 4,000 dedicated employees who deliver innovative medical technology solutions.But that’s just the beginning. Integra is growing at an unprecedented rate. We’re at a moment in time where the experience you’ll gain is more robust than the experience you bring. And we’re out to invest in your future because it’s the best way to maximize ours.At Integra, we firmly believe our people are our greatest asset and the foundation of our success. Our comprehensive Global Total Rewards program provides competitive compensation and benefits designed to keep our people healthy, motivated and engaged. Investing in our people through these programs is possible because of Integra’s ongoing commitment to our values and our shared success.Integra’s health as a company begins with the well-being of our people. Benefit programs vary by country, whether provided through company-sponsored insurance and programs, through statutory government programs, or a combination of both.Regardless of geographic location, our commitment is to offer the following, whenever possible
  • Benefit plans that meet all local statutory requirements
  • A range of programs that reflect typical local market practices
  • An opportunity for employees to tailor benefits to their specific needs
  • Benefits that balance employee’s short-term and long-term needs
Click HERE for more information regarding our benefits and total rewards program
  • Quality support for production (various production lines) and for various projects
  • Plan, coordinate and direct the quality aspects of process validation
  • Non-conformance management (initiation / evaluation / disposition on the batches / investigation)
  • CAPA management
  • Review and approve changes to documentation and processes
  • Work validation documentation in collaboratin with engineering (protocols, reports, process specifications, work instructions, pFMEA, master validation plan)
  • 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
  • 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
Loading ...
Loading ...

Deadline: 05-05-2024

Click to apply for free candidate

Apply

Report job
Loading ...
Loading ...

SIMILAR JOBS

Loading ...
Loading ...