Industrial Methods Technician – F/M

17/09/2024

Compensation and Logistics

  • Contact type: Full-Time Permanent Contract (CDI)
  • Status:  Non-Executive
  • Location: Clichy (subway line 13 or subway line 14, high-speed train service linking Paris to the suburbs : line RER C, train L, bus 74 or 341…)
  • Benefits: luncheon vouchers (€8.50 per day worked), health insurance (employer pays 50%), provident fund (employer pays 100%), travel pass (employer pays 50%) and 25 days of paid leave per year
  • Recruitment context: replacement
  • Partial teleworking possible (12 days/year)
  • Available from october 2024.

Please send your CV to: careers@corwave.com, reference « Industrial Methods Technician ».

Company description

CorWave is a medical technology startup, developing biomimetic implantable heart pumps with the goal of improving the survival and daily lives of patients with heart failure. 🫀🫁

The CorWave pump with undulating membrane is a disruptive technology protected by over 50 patents and 20 years of research. Funded by leading international investors, supported by renowned surgeons, with more than 85 employees of more than 13 different nationalities, CorWave aims to become a global leader.

The “EPIC” values are at the heart of the company’s success and drive CorWavers in this scientific, medical, industrial and profoundly human adventure: Each other together, Persist with passion, Innovate for patients and Cultivate trust.

 

Recruitment context

Are you looking for an exciting professional adventure within a dynamic company? We’re a passionate team that has made the leap from R&D 🔬 to industrial production. 🏭

Join us to be part of a committed industrial team, where innovation is our driving force and excellence our destination. 🤝

Our mission? To manufacture ultra-high-performance, ultra-reliable heart pumps to improve the lives of patients suffering from advanced heart failure. 👨‍⚕️

If you are ready to take on the challenge with determination, professionalism in an agile environment then this is the opportunity for you.

Welcome to the team where every beat counts!

 

Job description

As an Experienced NPI Technician, you will be responsible for providing technical recommendations to improve product manufacturing processes and implementing your recommendations during production, thereby contributing to their validation.

Your expertise will ensure the efficiency, quality, and compliance of the manufactured products while maintaining close collaboration with the development and quality control teams.

You will be responsible for the following tasks:

  • Contributing to the development of manufacturing and control processes
  • Working in tandem with the NPI Engineer, you will develop technical recommendations related to manufacturing processes
  • Contributing to the drafting of protocols and reports associated with the validation of manufacturing processes
  • Preparing work instruction sheets for manufacturing processes for the end user (operator)
  • Managing the production of pre-series products according to the work instruction sheets
  • Completing the Device History Record (DHR) for manufactured products
  • During production, you will share with the teams the improvements you have identified
  • Contributing to the drafting of non-conformity reports that arise during production and participating in root cause analysis
  • Contributing to the drafting of process FMEAs
  • Executing instructions from the NPI engineers.

Qualifications

  • You hold at least a BTS, DUT, Professional License, or bachelor’s degree (with a specialization in Lean Manufacturing)
  • You have a minimum of 5 to 10 years of experience in a similar role within the medical devices field or in various demanding environments with high production quality, such as aeronautics, aerospace, automotive, or other regulated mechanical industries
  • Proficiency in written and spoken English is recommended for this position (international environment).
Specific knowledge
  • You are familiar with electro-mechanical assembly.
  • You know and apply the best manufacturing practices for a Class III medical device. You are knowledgeable about risk analysis concepts (FMEA).
  • You have expertise in industrial drawing standards.
  • You can identify the causes of failures in manufacturing processes.You are familiar with electro-mechanical assembly.
Technical skills
  • You have experience in optimizing production, studying, and determining procedures for defined manufacturing processes.
  • You manage problem-solving methods and tools, oversee maintenance procedures, and design and create tools.
  • Proficiency in Microsoft Office (intermediate/advanced level) and SolidWorks or other CAD software (intermediate level) is required.
  • You also know how to use a microscope and specific production equipment for medical devices (such as sealing, cleaning, laser welding, etc.).
People skills
  • You exhibit rigor and have a strong sense of pedagogy (such as reporting, expressing dysfunctions, etc.).
  • You are curious and keep up with new technologies.
  • You demonstrate a team spirit
  • Take initiative in critical situations

Recruitment Process

  1. Pre-qualification (telephone or on Teams)
  2. Manager interview (on Teams or on site)
  3. Interview +Workshop
  4. Taking up references.