Career opportunities


Reporting directly to the Logistics Manager, after a training period and a personalized accompaniment, you will be autonomous and in charge of:

  • The preparation of orders.
  • Picking up products from the stock.
  • Handling the goods with care.
  • Washing and cleaning products.
  • Repackaging non-sterile products in the gray room.
  • Creating “product” labels.
  • Creating delivery and transport notes.
  • Control of orders.
  • To respect the rules of hygiene and safety.
  • To ensure that the stock of consumables is available and sufficient.
  • To ensure the proper use and maintenance of equipment.
  • To ensure that work areas are kept “clean and disinfected”.
  • To actively contribute to the good maintenance of storage areas.
  • To complete the documentary part related to these actions.

Work individually and in teams in a pleasant, relaxed and efficient atmosphere. Work in a controlled atmosphere.


  • Bachelor’s degree or Bac +2 / BTS (Transport and logistics services)
  • Licence pro management of logistics processes.
  • Wearing of PPE (Blouse, gloves, cap).
  • Computer skills: Sage, CodeSoft, Excel.
  • Versatility on other tasks of the logistics department. Work in interaction with several internal departments (Quality department, Purchasing…)

Send us your CV to the following address :


Based in Antony, France, SPINEVISION, a Medical Device company which provides innovative solutions for the treatment of various spinal pathologies, is looking for an Intern for the Regulatory Affairs & Quality Assurance department.

Provide support in maintaining the quality assurance system in compliance with the company’s quality policy and current regulations, in order to market effective and reliable medical devices for the safety of patients and users.

Provide support to the regulatory affairs department for the registration of medical devices in the different countries where the products are marketed.

  • Support in the constitution of technical files for the CE marking of products and keep the files up to date according to the regulations in force
  • Support in the creation of technical files outside Europe (Canada, Brazil, Australia, etc.)
  • Operational follow-up of the company’s design change and change control
  • Ensure the global follow-up of the quality indicators of the company’s processes
  • Follow the implementation of the data register in the framework of the RGPD
  • Participate in the normative and regulatory watch
  • All other missions that will be requested by the hierarchy
  • Bonus: Evaluate the feasibility of implementing a quality monitoring software

Master’s degree or equivalent in the medical, biomedical or pharmaceutical sector – focused on quality and regulatory affairs
Biomedical Engineering School, ISIFC, UTC…

Main skills:

  • Know the directives and regulations associated with medical devices
  • Know the documents and the quality process

Send us your CV to the following address :

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