Europeos.es : Inicio > Oferta de trabajo en Luxemburgo > director de control de calidad en industrias/directora de control de calidad en industrias > Senior Manager Quality Assurance & Product Compliance (m/f)
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Trabajos de director de control de calidad en industrias/directora de control de calidad en industrias en Luxemburgo
Senior Manager Quality Assurance & Product Compliance (m/f)
Clasificación del trabajo: Directores y gerentes › Directores y gerentes de producción y operaciones › Directores de industrias manufactureras, de minería, construcción y distribución › Directores de industrias manufactureras › director de fabricación/directora de fabricación › director de control de calidad en industrias/directora de control de calidad en industrias.
Traducción de la profesión: Führungskräfte › Führungskräfte in der Produktion und bei speziellen Dienstleistungen › Führungskräfte in der Produktion bei der Herstellung von Waren, im Bergbau und im Bau sowie in der Logistik › Führungskräfte in der Produktion bei der Herstellung von Waren.
Descripción de la oferta de trabajo:
What you'll do
Contribute to the creation and implementation of the strategy and development in
terms of Quality Assurance activities.
Establish the company's Quality Management System (QMS) compliance to ISO
standards, applicable regulations, and all associated tasks around Quality
Management
Support and collaborate with different internal departments in relation to
Operational Quality (Production Quality, Quality Control, Supplier Quality), including
participation in Quality Circle, support and overview of the CAPA activities.
Act as companVs representative for all activities related to product certification and
the registration of products in and outside the European Union
Carry out and/or support all risk management activities and conduct risk
assessments of processes and tasks
Ensure the conformity in terms of Safety Officer for Medical Devices
Develop and maintain strong relationships with internal and external stakeholders to
ensure optimal performance
According to Article 15 of the European Regulation (EU) 2017/745 for medical
devices, T
The PRRC (Person responsible for regulatory compliance) responsibilities are
according to the article 15 of the European Regulation (EU) 2017/745 for medical
devices
What you'll bring
Successfully completed master's degree in engineering
Diploma, certificate or other evidence of formal qualification, awarded on
completion of a university degree or of a course of study recognized as equivalent by
the Member State concerned, in law, medicine, pharmacy, engineering or another
relevant scientific discipline
5 years of experience, ideally in regulatory affairs or in quality management systems
relating to medical devices
Work experience in an international and multicultural environment
Excellent leadership and management skills
Ability to manage cross-functional teams and to collaborate with business partners
across multiple functions
Planning and organization skills
Strong communication skills — written, verbal and presentation
Competent in problem solving, team building, planning and decision making
Attention to detail
Commercially aware
Mircosoft suite
Languages: English is mandatory any other language will be appreciated.
Our Offer
Become part of a company that makes a positive contribution to launching
groundbreaking scientific developments and therapies.
Contribute to innovative cell therapies and be a part of revolutionary cancer
therapies.
Take advantage of the operational opportunities in a growing, modern, and
innovative company within the health care/life science industry.
Experience an intensive exchange of experiences and close cooperation in a
worldwide network with our customers, friends and partners.
We offer participation in national and international company events.
After your initial training, you will receive regular training and further education
opportunities that are tailored to your needs.
A workplace that promotes your maximum.
You will participate in capital-forming benefits, numerous corporate benefits.
33 days of vacation.
Positive corporate culture and practiced teamwork across all locations.
Individual development opportunities of your international competencies and
language skills.
País del trabajo: Luxemburgo.
Número de puestos: 1.
Nivel educativo: Máster o nivel equivalente.
Experiencia: 5 años.
Empleador: B Medical Systems S.à r.l..
Instrucciones para solicitar:
Oferta de trabajo obtenida del portal Eures, con fecha 10 de Julio de 2024, y con identificador de la vacante:PES_LU_724726.
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