Production Supervisor – F/M

20/12/2024

 

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: job creation
  • No remote work possible for this position
  • Available from: January 2025.

To apply, please visit this page: Link to the job posting

Company description

CorWave is a medical technology start-up developing biomimetic implantable heart pumps with the mission to improve the lives of patients suffering from advanced heart failure.

The CorWave membrane pump is a breakthrough technology, protected by more than 50 patents, and the result of 20 years of research.

Funded by leading international investors and supported by renowned surgeons, CorWave aims to become a global leader.

More than 90 CorWavers from 13 different nationalities are driving this scientific, medical, industrial, and deeply human adventure.

Recruitment context

Are you looking for a new challenge in an innovative and dynamic company?

Join our committed team, which has transitioned from R&D to advanced industrial production.

Our mission: to design and manufacture ultra-high-performance and reliable heart pumps, dedicated to improving the lives of patients with advanced heart failure.

If you are motivated, ready to innovate, and excel in an agile environment, this adventure is for you.

Join us, where every heartbeat makes a difference!

Job description

As a Production Supervisor, you will play a key role in managing production activities within a Controlled Atmosphere Zone (ZAC).

Your main mission will be to supervise the teams (3 Operators currently, with 4 more Operator profiles joining by January 2025), ensure compliance with production processes, and guarantee the achievement of quality and productivity goals.

You will be responsible for the following tasks:

Operational Management (30%):

  • Manage the production operators, organize, and coordinate their activities within the ZAC
  • Participate in the onboarding and training of new arrivals, while transferring the necessary skills
  • Monitor individual performance and ensure a high level of motivation within the team.

Monitoring Production Schedules:

  • Ensure adherence to production schedules and adjust priorities according to production needs
  • Collaborate with the Production Manager to ensure the optimization of resources and delivery timelines.

Handling Anomalies & Communication:

  • Identify and document anomalies or malfunctions encountered during the production process
  • Report key information to hierarchical managers and propose corrective actions to improve processes.

Production Supervision (70%):

Managing Production Processes:

  • Supervise assemblies and sub-assemblies while strictly following technical files and work orders
  • Ensure parts compliance, component availability, and the smooth running of production operations
  • Ensure the visual and three-dimensional inspection of the produced assemblies and sub-assemblies.

Compliance and Quality:

  • Ensure the application of Good Manufacturing Practices (GMP) for Class III medical devices
  • Check and validate the records of the DHR (Device History Record) and monitor non-conformities throughout the process via NMR (Non-conformity Management Report).

Continuous Improvement:

  • Actively participate in the continuous improvement of production procedures
  • Propose initiatives to optimize team and equipment performance and productivity.

Maintenance and Safety:

  • Perform first-level preventive maintenance of equipment and ensure a clean and safe working environment
  • Enforce and comply with safety instructions within the ZAC.

Qualifications

  • You hold a BTS, DUT, or a minimum of a professional bachelor’s degree
  • You have between 7 and 15 years of minimum experience in a similar position in the medical device field or in varied and demanding environments (high production quality) such as aeronautics, aerospace, automotive, or other regulated mechanical industries
  • Previous experience in team management, ideally in a clean room or high-quality industrial environment.
Specific knowledge

Knowledge of GMP and regulations for Class III medical devices.

Technical skills
  • Mastery of specific production equipment (microscope, sealing, cleaning, laser welding, etc.)
  • Experience in planning and project management (PDCA approach: Plan-Do-Check-Act)
  • Ability to organize and coordinate projects to achieve production goals.
People skills
  • Leadership
  • Rigor
  • Team spirit

 

Recruitment Process

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