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Group Quality Manager - In Vitro (M/F)

HAYS

08.06.2022 | Porto | Referência: 2046029


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Hays
Group Quality Manager - In Vitro (M/F)

Porto

Your new company



The Group Quality Manager is responsible for developing, deploying and maintaining the Group Quality Management System in line with our aspiration, the promises we make and the needs of the markets we serve.



Your new role




  • Participate to the development of a strong Quality Culture from the company’s executive management to the rest of the organization.

  • Drive the standardization and harmonization of quality related processes for the entire group.

  • Ensure that where required that our laboratories and other operations such as radiology units are fully accredited via the generalization of best practices.

  • Ensure the correct definition and follow up of quality KPIs in our service offerings.

  • Ensure that quality related incidents are investigated and followed up in a systematic way across all geographies.

  • Drive the implementation of digital solutions with respect to quality related processes (e.g. complaint and incident management) and other operational processes that impact customer satisfaction and / or the overall compliance level



  • Lead projects that impact the QM strategy or the organizational structure, being responsible for the implementation of the projects within the given framework (time, budget, quality) and manage the projects through KPIs.

  • Highlight potential threats and opportunities for quality through systematic risk assessment.

  • Facilitate the communication and sharing of best practices and good examples.

  • Support a culture of continuous improvement throughout the organisation.




What you will need to succeed




  • Master’s Degree in a technical/ process engineering/QA discipline, Advanced Degree preferred, with significant related professional experience preferably within the healthcare environment.

  • Fully versed in ISO 15189, ISO 17025 and ISO 9001

  • Ideally with experience with in-vitro diagnostic directive and/or regulation

  • Demonstrated in-depth knowledge in quality process mapping and development

  • Demonstrated ability to affect change.

  • English fluent as a must (presenting, writing, reading). Minimum Years Recommended and/or Preferred: 5-7 years



  • Solid interpersonal skills and relationship management



  • Outgoing and dynamic. Comfortable working in a flat non-hierarchical environment.

  • Rigorous, organized, autonomous.




What the company can offer you



Be part of one of the main multinational companies in the pharma industry.

Good Salary Package.

Possibility to grow.



Next step



If you are interested in this opportunity, click on "Send application" to send us your updated CV.

If this is not what you are looking for, contact us to talk about other career opportunities, always in an absolutely confidential manner.

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