Quality Specialist - Breda

Vacancy information

Publication date:November 20 2020
Employment type: Permanent
Sector: Medical Devices
Function Group: Quality/RA

Function Group: Quality/RA / Quality Specialist

Organization

For a global leader in the bioprocessing industry, we are looking for a Quality Specialist. The organisation is a global leader in the field of filtration products and the industries they supply to include medical devices, biotechnology, and pharmaceutical. By supplying these key industries, the organisation has an essential role and aims to improve product quality and safeguard health throughout the entire product lifecycle. Currently, they are scaling up their production activities in the Netherlands by making this their main manufacturing location for the EMEA region. Within this role as Quality Specialist, you will be part of the quality department, setting the quality standard with a newly established team, and be at the forefront of a great adventure full of potential.

Function

As Quality Specialist, you wil report directly to the Quality Assurance Director and participate actively in the ISO 13485 quality management system. Together with colleagues you carry the responsibility of quality reviews, product release of MPR’s that include verification of raw materials, and the evaluation of quality control testing.

Next to those main tasks you carry the responsibility of a big variety of tasks like:

  • Batch record review
  • Oversee complaints, deviation and non-conformances and deviations.
  • Label verification
  • Attend daily meetings
  • Mentor quality associates I personnel
  • Generate, review and approve quality investigations
  • Be part of maintaining the quality management system

Requirements

We are looking for a candidate with the following profile:

Mandatory requirements:

  • BSc of science (or a related field)
  • 2+ years of experience with ISO 13485 or GMP
  • Experience in a production or manufacturing environment
  • A background in the medical devices, pharmaceutical or biotechnology sector

Preferred requirements:

  • Internal Audit certification
  • Experience with good documentation practices

Offer

If you are a result-driven professional and want to make a difference in the world, our client is the perfect fit for you.

The organisation can offer:

  • Monthly salary between €3.000 to €4.000 depending on your experience
  • Non-contribution pension scheme
  • Social securities
  • Travel reimbursements
  • Holiday allowance of 8%
  • 26 holidays
  • An environment of meaningful innovation and ambitious professionals
  • Opportunity for personal and professional growth

Application

If you are interested in this job, or in similar ones, please feel free to contact me directly.

Joep Visser

Senior Associate | Medical Devices

+31(0)6-82635527

+31(0)23-7548660

j.visser@qtcrecruitment.com

Apply

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