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Quality Assurance Manager Distribution Center

SIRE Life Sciences®

Netherlands, zagranica

SIRE Life Sciences®

Quality Assurance Manager Distribution Center

Location: Netherlands

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Medical Devices organization, based in Netherlands.

The corporate company decided to set up their own distribution center as a result of continuous expansion and growth. This client is an international organization which is active in various industries. As for healthcare, the company is playing a major part as they offer reliable, efficient logistic and supplier solutions for the distribution of medical devices and healthcare products.

ROLE DESCRIPTION

In your role as Quality Assurance Manager, your main responsibility is to overview and maintain the Quality Assurance of healthcare products at the distribution center. You are the direct support to the distribution site director. As a manager you will become a mentor, in which you distribute your knowledge and experience to both internal and external stakeholders. This involves Quality Assurance documentation which does not only include ISO certifications. In addition, this also includes regulations related to the spread of medical devices. Furthermore, you will receive the opportunity to develop your own leadership strategy and create your own vision of the site with the ultimate challenge to improve the quality system. As this role directed to the set up of the processes within the distribution center, this project will at least take a year with possible extension to two years.

RESPONSIBILITIES

* Apply and improve Quality Management System
* Maintain and apply QA standards and compliance in relation to global and European regulations
* Identification of discrepancies in CAPA and offering solutions
* Development of quality improvement processes and creation analytic tools.
* Preparation and supervision of internal and external audits
* Creation of objectives and strategies validating Quality Assurance

REQUIREMENTS

* BA in Life Sciences
* 6 years of experience within Quality Assurance and Regulatory Affairs within the Medical Devices sector
* 3 years of experience within a management role in Medical Devices company
* Knowledge of ISO 13485 into detail
* Experience with Risk and change management
* Fluency in English and Dutch
* Experience with QMS and MMD principles

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Juliette van Kraaij.

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SIRE Life Sciences®

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