Proposal
Would you like to learn how the Quality Management department Works in an industrial company within the In-Vitro Diagnostics sector?
Our QA team is looking for someone keen to learn and develop professionally within a company specializing in plastic injection molding for the healthcare sector.
You will have the opportunity to gain practical training in the operation of a Quality Management System, work in a regulated environment and collaborate with different departments. Furthermore, you will gain first‑hand insight into the working of a multinational company such as Werfen, a leader in the In‑Vitro Diagnostics sector, and learn in a real, highly regulated industrial environment.
Main responsibilities
* Assist in the management and updating of Quality System documentation.
* Contribute to activities related to ISO 13485 regulatory compliance, familiarizing yourself with the requirements of the Quality Management System.
* Interact with other departments to ensure compliance with quality requirements.
* Participate in the management of non-conformities and the monitoring of corrective and preventive actions (CAPA).
* Assist in the management of customer complaints and the preparation of internal audits.
Secondary activities
* Contribute to continuous improvement initiatives and the review of internal processes.
* Participate in the monitoring of quality indicators and data analysis.
* Take part in cross‑functional activities within the Quality Department, gaining a comprehensive overview of the department’s day‑to‑day operations.
Education
Undergraduate or postgraduate student studying for a degree in technical or scientific subjects, with an interest in quality management and the industrial sector.
Skilss & competencies
* Proactive attitude
* Initiative
* Strong willingness to learn
Working hours
Schedule to be agreed, preferably in the morning.
Additional requirements
Own vehicle is required to commute to the workplace.
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