Position: Mid-Senior level

Jobtyp: Full-time

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Jobinhalt

You are an expert in Quality management and quality standards such as all ISO standards. Knowledge of GxP regulation is a plus. You have excellent coordination skills, communication, and people management skills. You enjoy working in a fast-paced environment, and you welcome challenging experiences. Leading for success is your style, and you are ready for the next step in your career. If all of this describes you, then keep on reading!
Your Role

As a Quality Manager, you will be responsible for improving, and monitoring the existing Quality management system. You would need to ensure that the above is done in line with the international quality standards and by the strategic objectives of the sites in Geel, Eindhout, Tessenderlo, and Liège. You manage a team of quality people and support them in their daily job. You will have direct contact with quality experts of our customers with whom you will jointly evaluate all quality-related actions and issues.
Your Responsibilities
  • Coordination and management of external Quality inspections and audits (performed by legal entities, customers, notified bodies, …) to maintain/achieve the existing/new licenses and certificates;
  • Securing the legal compliance of all Quality Management relates aspects, including:
  • Management of the pharmaceutical permits in cooperation with a Qualified Person
  • Securing all Quality requirements during the implementation of new customers/projects
  • Realization of the quality KPIs of the multiple customers and linked to this, the supervision of the root cause analysis and the implementation of structural improvement actions in response to customer complaints and deviations detected during internal quality control in cooperation with the relevant department managers;
  • Coordination and management of the internal audit process and the document management system, incl. correct usage of it by the different process owners;
  • Advise senior and local management on Setting Quality compliance objectives and ensure targets are met;
  • Manage a team of quality experts and support them in their day-to-day job. Set direction to your team and ensure they can develop;
  • Support Quality Management Review (QMR’s) meetings according to the certified standards;
  • Identify strategic weak points of the Quality system and development of improvement measures, if applicable in close cooperation with the responsible BU/FU.

Your Skills And Experiences
  • You have a Master degree or similar;
  • You have at least 3 years of experience in a management position and are an experienced leader;
  • You have a profound knowledge of the different management systems :
  • Minimum: ISO9001, ISO14001, and preferably OHSAS 18001
  • Preferably: GXP, ISO13485
  • You are a born communicator skilled in bringing different stakeholders together and aligning them. You can make clear agreements and proper adjustments when required;
  • You have an analytical mindset, and you can investigate root causes and CAPA’s and dig into legislation and international standards;
  • You speak Dutch and English fluently, French is a plus;
  • You are customer-oriented.
Good Reasons to Join

We offer a solid position within a strong international environment with a competitive salary and opportunities for further development within the Kuehne + Nagel Group. You will be part of the Management Team of Business Unit Pharma & Consumer Belux with direct reporting to the Business Manager Pharma and Consumer. Please contact us for more information. req78561

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Frist: 10-01-2026

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