Manufacturing & Equipment Supervisor - Medical Devices - Liège


Our Client is a is an innovative medical device company based in Mont-saint-Guibert with a Production site in the area of Liège (but also in Israël and Australia) that is currently developing a novel neurostimulation technology to treat Obstructive Sleep Apnea (OSA). The mission of the company is to provide their users, with the freedom to enjoy life to its fullest by delivering reliable, durable and harmonious solutions to treat OSA.


You are looking for a professional challenge that allows you to work in a start-up environment in order to participate to the technology transfer and improvement of manufacturing activities?
You want to bring your expertise in order to improve manufacturing activities in GMP and/or ISO 13485 environment? You want to endorse polyvalent responsibilities in order to contribute to face a scaling-up phase?
Plus One can offer you this great challenge:

Your Responsibilities:

  • Lead different engineering activities, including maintenance of unique manufacturing equipment, with both internal operation team and external manufacturers.
  • Analyze and recommend improvements to all production process and methods to facilitate capacity, cost reduction and quality improvements.
  • Investigate equipment or manufacturing process related issues.
  • Create/update product drawings, manufacturing documents, BOM, etc..
  • Proactively identify issues, troubleshoots, and escalates concerns as appropriate.
  • Communicate requirements for validation execution and documentation.
  • Promote projects with external manufacturers.
  • Perform other duties assigned as needed.
  • Coordinate the maintenance activities, including facilities management.


Professional skills Requirements:

  • Mechanical , Electro-Mechanical, Biomedical Engineering Master/Bachelor Degree.
  • At least 3 years of experience in a Manufacturing/Process/Maintenance role.
  • A first experience in a highly regulated environment (GMP), Clean Room, Medical Device industry is preferred
  • Demonstrated knowledge of operation principles and practices, and procedures.
  • Hand’s on technical experience - (HVAC systems, Chiller, environment monitoring systems) -advantage
  • Experience in small projects execution
  • Experience working with international suppliers
  • Ability to work cooperatively with coworkers and the public.
  • English & French - High level (Verbal and non-verbal)
Personal Skills Required
  • Proactive, good communicator and innovative
  • Ability to work independently while within a group framework
  • Flexible (as the position requires to travel abroad)
  • Excellent proficiency in English (verbal and written).
  • Effective communication skills
  • Self-motivated, self-maintained and able to take the initiative to solve problems
  • Committed to follow company policies and procedures, follow cGMP and other regulatory requirements.


Our Client offers a full-time permanent position along with an attractive remuneration package.

The position is based in Belgium and has an international scope.

This is an agile start-up company culture focused on values of entrepreneurship, engagement, integrity, passion and team spirit.

Publication date


Contact person

Gaëlle Minet

All vacancies
Plus One uses cookies to remember certain preferences and align jobs interests.