Vacature Quality Technician in Schiphol-Rijk

  • Referentie nr.: HK.1725-UZP-NL-FPC-050319
  • Geplaats op: 2025-03-05
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Vacature omschrijving



Organisation

Working at a leading pharmaceutical company where quality comes first. A place where you can grow in your role and as a person. Being part of a large international organization that still maintains short communication lines and a family-oriented culture. You have already taken your first steps in quality regulation and are familiar with MDR and ISO13485 guidelines, but you are looking for an environment where you can learn even more. Don't wait any longer—apply now!

As one of the most well-known and respected eye care brands in the world, we offer the broadest and best range of eye health products, including contact lenses and lens care solutions, pharmaceuticals, intraocular lenses, and other eye surgery products. The location where you will be working is responsible for storing and preparing eye care solutions for transport.

You will be part of the QA team. Within the hierarchy, you will report directly to the Senior QA Manager in your unit and the QA Director. The entire QA department consists of seven employees. The team is highly engaged in their work, and a positive atmosphere is key—there is room for jokes, enjoyment in the job, and looking out for one another.



Job Description

Working at a leading pharmaceutical company where quality comes first. A place where you can grow in your role and as a person. Being part of a large international organization that still maintains short communication lines and a family-oriented culture. You have already taken your first steps in quality regulation and are familiar with MDR and ISO13485 guidelines, but you are looking for an environment where you can learn even more. Don't wait any longer—apply now!

In this role, you will be responsible for collecting and assessing data related to MDR (Medical Device Regulation) guidelines and legislation. Bausch + Lomb is an international company with many suppliers, and this is exactly where you will play a crucial role. Thanks to your involvement, we will have a clear understanding of which suppliers and products comply with MDR regulations and which do not. You will gather the necessary information and process it in our systems and Excel.

Your key tasks will include:

  • Setting up and managing processes that comply with MDR requirements for distributors and importers.
  • Assisting in the management and maintenance of the product restriction table (products temporarily prohibited from shipment).
  • Acting as the main point of contact for manufacturers, Regulatory Affairs (RA), and authorized representatives.
  • Updating and maintaining key product data.
  • Ensuring that approved products can be shipped to customers.

We believe that by giving talented people the right opportunities and on-the-job guidance, they can grow. This is currently a temporary position, but if you perform well, other opportunities may arise within this large international company.

This role involves frequent meetings with colleagues and suppliers abroad. As a result, you may occasionally need to attend meetings outside of regular working hours. After the initial training period at the office, you will have the flexibility to organize your work schedule.





Job Requirements

You are someone who works meticulously. Quality is your priority, and you can effectively communicate this to your colleagues. You are eager to learn, focused on self-development, and want to do so in an international environment. Data is no mystery to you, and you enjoy working with it extensively.

Additionally, you bring the following qualifications:

  • A completed MBO/HBO degree and experience with ISO13485 and/or MDR.
  • Proficiency in Microsoft Excel.
  • Strong communication and writing skills in English (company language).
  • Availability for 37.5 hours per week and willingness to occasionally work outside office hours.
  • Residence in the Netherlands and willingness to be on-site full-time for the first few months.
  • Familiarity with and/or interest in MDR laws and regulations.
  • Experience with quality management systems.




Salary and Benefits

At Bausch + Lomb, you are at the center of our organization. As part of our community, we offer you the following excellent employment conditions:

  • A one-year contract for 37.5 hours per week.
  • A competitive salary based on your experience and educational background.
  • A travel allowance of €0.23 per kilometer (up to 70 km) or full reimbursement for public transport.
  • A 13th-month salary and 8% holiday allowance.
  • 25 vacation days based on a full-time contract.
  • Free contact lenses through the Bausch + Lomb lens program.
  • A fun Social Club that organizes multiple activities throughout the year.




Ref.nr.:HK.1725-UZP-NL-FPC-050319 - RT180494901

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