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Technical Advisor - Automotive - Brussels

Based in Brussels (Belgium), FIGIEFA is the European federation and political representative of the independent wholesalers and retailers of automotive replacement parts. Together with its 19 national European Member State members, it represents the interests of more than 30.000 companies trading with vehicle parts, components and accessories throughout Europe.

The aim of FIGIEFA is to safeguard a legislative environment in the EU that provides access to technical information, to the ‘connected vehicle’ and its in-vehicle data as well as to replacement parts/equipment as the basis for free and fair competition in the automotive aftermarket in a rapidly changing automotive technology environment.

In order to support the activities of its office in Brussels, we are currently looking for a (m/f):

Technical Advisor

Responsibilities:

As a Technical Advisor, you manage all technical and ‘connected vehicle’ IT-related dossiers and processes in connection with FIGIEFA’s activities in the area of the automotive aftermarket.

Your main responsibilities are:

  • Advise FIGIEFA in all technical and ‘connected vehicle’ IT-related matters.
  • Participate in meetings (in Brussels or EU) and take responsibility for the management of technical subjects and dossiers (e.g. telematics, EC type-approval legislation).
  • Support the FIGIEFA Secretariat in its information activities and meetings.
  • Advise and prepare answers on upcoming questions from the EU institutions and help in the preparation of position papers.
  • Liaise with FIGIEFA’s partner alliance AFCAR (Alliance for the Freedom of Car Repair in the EU).
  • Communicate with FIGIEFA legal/political experts and work out common strategies, statements, papers and positions.
  • Report results and work evolution on a regular basis.
Profile:
  • You are an experienced automotive technical expert or are experienced in vehicle-related IT technologies around the ‘connected vehicle’ (e.g. telematics and cybersecurity).
  • You are, preferably, specialised in vehicle communication, vehicle design/functionality, diagnostics or contemporary and developing vehicle technologies.
  • You have excellent oral and written communication skills in English and strong interpersonal skills.
  • You are flexible, proactive, and able to work on your own as well as in close cooperation with the FIGIEFA Secretariat.
  • You are able to assess the business consequences of new legislation, automotive technologies and vehicle related services.
  • You are ready to travel frequently to other European countries.
Offer:
  • A challenging position within a multi-national and political environment that tackles a wide range of technical issues.
  • The opportunity to support and promote free and fair competition in the automotive aftermarket and to safeguard a legislative environment at EU level.
  • Various contacts with European and international institutions while representing the interests of FIGIEFA members.
  • An attractive salary package in line with the position responsibilities and your experience.

Senior R&D Project Leader - Medical Device - Awans (Liège)

Founded in 2009, CryoTherapeutics is an early stage European innovative company that is now establishing its operations in Liège (Awans). The company is in the process of developing a novel catheter system to treat atherosclerotic plaque that causes heart attacks by delivering cryoenergy to the coronary arteries. For additional information about the company, please visit http://www.cryotherapeutics.com/

CryoTherapeutics aims to develop and market the novel cryoenergy therapy initially for patients who have suffered a heart attack, and in the longer term also for patients identified as being at future risk of heart attack. CryoTherapeutics recently raised 7M€ in its latest round of financing and will use these funds to continue development of this technology with the aim of starting clinical studies later this year.

In order to support the expansion of the team in Awans, we are looking for a (m/f):

Senior R&D Project Leader

Responsibilities:

As a Senior R&D Project Leader, the candidate will lead strategic R&D projects, including software and hardware components and equipment. Reporting to the CTO, the candidate will lead innovation throughout the company.

The positions’s main responsibilities are:

  • Lead strategic R&D projects from concept to commercialization including specifications, design, prototype, industrialisation, manufacturing, and commercial release of software driven electromechanical systems.
  • Ensure resources, processes, procedures and controls are adapted to the projects needs.
  • Lead internal and external project teams with respect to timelines, budgets, quality, safety and business requirements.
  • Analyse the market, select, lead and manage supppliers, vendors, contractors and external partners in order to meet the innovation goals.
  • Understand medical safety requirements, FMEA and risk analysis. Prepare validation plans in line with company documentation, CE and FDA requirements and industry standards.
  • Lead compliance to the Quality Management Systems (ISO 13485 environment).
  • Be a key person of contact for KOL, scientific experts and governmental authorities.
  • Develop appropriate test methods and write protocols and related reports,
  • Report results and work evolution on a regular basis to the top management.
Profile:
  • Engineering Master’s degree in Electronics, electromechanical or related fields.
  • At least 7 years experience in R&D positions within small and large medical devices companies.
  • Expertise in hard- and software technologies and, ideally, also in catheter engineering, including equipment and software validations
  • Excellent project management methodologies and tools.
  • Strong leadership and communication skills together with hands-on and pragmatic mind-set.
  • Proven record of dealing with vendors for electromechanical and software based systems for medical devices,
  • Very good organizational, analytical and problem solving skills.
  • Highly collaborative, self-motivated and team-oriented individual in a company setting.
  • Excellent oral and written communication skills in English. Any other language is a plus.
  • Prone to travel up to 20% of your work time.
  • Despite joining at senior level, be a hands-on person and can lead and manage the team as well as perform some of the work at task.
Offer:
  • A challenging position with a high potential innovative and young medical device company.
  • To work in a human-sized, collaborative and respectful environment
  • Work within a dynamic and experienced team that brings the best out of motivated potentials.
  • An attractive compensation package in line with the position’s responsibilities and your experience.

Quality Assurance Manager - Medical Device - Liège

Founded in 2005, Graftys develops, manufactures and markets patented synthetic bone biomaterials for reconstructive orthopedic surgery. Graftys is specialized in new generations of resorbable calcium-phosphate cements and is based on the research works of Pr. Jean-Michel Bouler (CEISAM/CNRS). 

The Company’s key products are commercialized in more than 25 countries, including Europe and the USA, through distribution partnerships. The objective of Graftys is to expand the company product lines by offering new versions of existing products and new products with enhanced regenerative properties.

Graftys, one of the world leaders in resorbable bone cements, is based in Belgium and France. For more information about the company, please visit https://www.graftys.com 

In order to support the expansion of the dynamic team in Liège, we are looking for a (m/f):

Quality Assurance Manager

Responsibilities:

As a Quality Assurance Manager, you contribute to the implementation of a quality assurance system. Reporting to the Site Director, you establish, implement and maintain an efficient and cohesive quality management system that ensures compliance with the ISO, FDA & MDSAP requirements

Your main responsibilities are:

  • You manage batches activities related to manufacture and testing of medical device in order to ensure compliance with internal and regulatory requirements.
  • You are responsible for quality assurance organization, which consists in:
    • Quality Systems, Metrics, Management Review, Internal/External Audits, Change Controls, …
    • Training, Documentation Control, Product Lifecycle Management, …
    • Complaints, Recall…
  • You monitor and report the performance of the quality management system to the Executive Management.
  • You ensure partnership with Regulatory team in order to develop, support and execute compliance related strategies.
  • You closely collaborate with Production team in order to ensure quality system enables design and manufacturing success while maintaining compliance.
  • You contribute to the continuous improvement of the quality management system.
Profile:
  • You hold a Master’s in Industrial Pharmacy, or a PhD in biomedical sciences, biochemistry, life sciences, etc.
  • You are ideally QP registered.
  • You have at least 5 years’ experience in production in the life sciences, ideally in the medical device industry.
  • You have experience with FDA Quality Systems Regulations, ISO 13485:2016, Quality Certificates and MDSAP.
  • You are able to foster a positive culture of growth, collaboration, and achievement across the organization.
  • You are rigorous, independent, pro-active and versatile.
  • You are a team player with a good oral and written communication.
  • You are fluent in French and English.
Offer:
  • A challenging and rewarding position within a fast-growing company.
  • The opportunity to join a company specialized in innovative products for reconstructive orthopedic surgery.
  • To work in a human-sized, innovative, collaborative and dynamic company.
  • An attractive salary package in line with your experience.

Scientific & Business Development Manager - Medical Device - Gosselies

Founded in 2005, Graftys develops, manufactures and markets patented synthetic bone biomaterials for reconstructive orthopedic surgery. Graftys is specialized in new generations of resorbable calcium-phosphate cements and is based on the research works of Pr. Jean-Michel Bouler (CEISAM/CNRS).

The Company’s key products are commercialized in more than 25 countries, including Europe and the USA, through distribution partnerships. The objective of Graftys is to expand the company product lines by offering new versions of existing products and new products with enhanced regenerative properties. 

Graftys, one of the world leaders in resorbable bone cements, is based in Belgium and France. For more information about the company, please visit www.graftys.com.

In order to support the expansion of the dynamic team in Gosselies, we are looking for a (m/f):

Scientific & Business Development Manager

Responsibilities:

As a Scientific & Business Development Manager, your mission is to analyze the market and internal data, to manage the R&D projects grants and to elaborate the business plan and budgets. You directly report to the CEO.

Your main responsibilities are as follows:

  • You analyze the biomaterials and bone tissue engineering market trends & evolutions.
  • You determine production costs and suggest optimization options based on market analysis and on prices, and reimbursement trends.
  • You write/defend research projects (R&D, Preclinical, Industrialization, Clinic, etc.) in French and English.
  • You manage funded projects by providing scientific reporting, financial statement of claim and administrative (IP, confidentiality…) monitoring.
  • You elaborate business plans at 5-8 years, and you build consolidated budgets.
  • You organize the budget process: collect, analysis and summary of budgets data.
  • You report work evolution to the top management in a structured way.
Profile:
  • You hold a MD, a DVM, or a PhD in biomedical sciences, or pharmacy. An MBA (or equivalent) is a plus.
  • You have a first experience in high-end consulting or in business development in the field of implantable medical device (ideally), biotech or pharma.
  • You ideally have a good knowledge of national and international laws and requirements in the field of implantable medical devices.
  • You have strong analytical and synthesis skills.
  • You have a strong business orientation mindset.
  • You are rigorous, independent, pro-active and versatile.
  • You are a team player with a good oral and written communication.
  • You are fluent in French and English.
Offer:
  • A challenging and rewarding position within a fast-growing company.
  • The opportunity to join a company specialized in innovative product for reconstructive orthopedics.
  • To work in a human-sized, innovative, collaborative and dynamic company.
  • A full-time permanent contract (CDI) with an attractive salary package in line with your experience.

Research Assistant – Flow Cytometry and Serology - Bio-Pharma/Biotech - Gosselies

Caprion Biosciences is a contract research organisation with facilities in Montreal (Canada) and Gosselies (Belgium). Caprion Biosciences offers analytical services to biopharmaceutical companies ranging from mass spectrometry-based analytical services to the characterization of the human immune response in clinical samples.

Caprion Biosciences operates globally, with partners in North America, Europe and Asia, including large pharmaceutical companies and biotech companies.

In the context of its growing immune monitoring service offering in Gosselies (Belgium), we are looking for a (m/f):

Research Assistant – Flow Cytometry and Serology

Function :

Reporting to the Laboratory Manager and working closely with Principal Scientists, you work within a team focusing on the characterization of the cellular (ELISPOT and various flow cytometry assays such as phenotyping of PBMC, detection of intra-cellular cytokines, etc) and of the humoral (ELISA, Luminex, viral neutralization tests, etc) immune response.

Your tasks include :

  • Perform immunoassays according to current standard operating procedures;
  • Participate to the writing and/or to the review of method SOP and worksheets;
  • Manage reagents inventories and orders;
  • Participate to the technical management of the laboratory;
  • Perform work according to internal quality standards, apply relevant Quality System procedures and participate to the continuous improvement of Quality documents;
  • Attend relevant internal training activities;
  • Depending on the experience level of the candidate, additional tasks may include:
    • Act as a leader in the laboratory for specific studies;
    • Work with the Principal Scientist to prepare experimental plans needed for the conduct of immune monitoring assays;
    • Participate in the development and qualification/validation of complex methods;
    • Participate in experiment planning and problem solving.
Profile:
  • You hold a bachelor degree or a master’s degree (or the equivalent) in a life science discipline such as biology, medical biology or biochemistry/biotechnology
  • You demonstrate a relevant laboratory experience.
  • You have theoretical and practical knowledge of techniques related to cellular and humoral immunology. Experience in cell culture and handling infectious materials in BL2+ environment is an asset.
  • You demonstrate excellent organisational skills.
  • You demonstrate schedule adaptability and flexibility.
  • You are willing to actively participate to the generation, the implementation and the continuous improvement of laboratory processes.
  • You are willing to work in a Quality environment (ISO17025, GCLP, GMP) and apply good documentation procedures (GDP).
  • You are functional in French (spoken and written) and have a functional knowledge of written English. Knowledge spoken English is an asset.
Offer :
  • Diversified tasks and responsibilities and interesting projects.
  • A professional, dynamic and stimulating work environment.
  • Continous training and development opportunities.
  • A competitive salary package including benefits, adapted to your experience and the context.
  • Full time permanent contract, with possibility of rapid start.

Clinical Research Associate/Manager - Bio-Pharma/Biotech - Awans

Founded in 2009, CryoTherapeutics is an early stage European innovative company that is now establishing its operations in Awans (Liège). The company is in the process of developing a novel catheter system to treat atherosclerotic plaque that causes heart attacks by delivering cryoenergy to the coronary arteries. For additional information about the company, please visit http://www.cryotherapeutics.com/

CryoTherapeutics aims to develop and market the novel cryoenergy therapy initially for patients who have suffered a heart attack, and in the longer term also for patients identified as being at future risk of heart attack. CryoTherapeutics recently raised 7M€ in its latest round of financing and will use these funds to continue development of this technology with the aim of starting clinical studies later this year.

In order to support the expansion of the team in Awans, we are looking:

Clinical Research Associate/Manager

Responsibilities:

Reporting to and working closely with the Chief Medical Officer, as Clinical Research Associate/Manager, you are responsible for the operational management and the oversight of clinical trials according to the clinical strategy.

Your main responsibilities are :

  • Support and manage clinical trials for company, including protocol writing, clinical investigation reports, site selection and qualification of investigators.
  • Facilitate and support physician training for initiation of the trial, Site Initiation Visits, patient enrollment according to protocol inclusion criteria and site monitoring.
  • Assist in clinical cases and ensure that physicians and staff are well trained and educated with regards to patient selection, treatment planning, optimum use of system, etc.
  • Site monitoring, including scheduled visits, events reporting and documented interactions with clinical sites
  • Compiles required clinical documentation for regulatory submissions including patient consent forms, contracts and monitoring plans.
  • Work closely with the research team to ensure that all protocol required procedures and visits occur according to protocol specified guidelines and timely entry of the data in the electronic database.
  • Represent the company in all regulatory and third party audit requests for clinical trial information.
  • Deal with product-related site request and solve issues.
  • Engage with physicians and clinical staff, build relations and credibility to be a high level spokes partner.
  • Create and maintain effective partnerships with KOL.
  • Report results and work evolution on a regular basis to your line manager.
Profile:
  • Master’s degree in Biomedical Sciences, Bioengineering or any related field.
  • 4-7 years minimum in the management of pre- and post-market medical device studies (class III) at country or European level.
  • Experience in clinical trial protocol writing, support for cardiovascular medical devices, and ability to manage cases in cath lab.
  • Experience introducing disruptive technology, which somehow changes the way clinicians operate.
  • Experience in directing, training physicians and staff to stand-alone level.
  • Flexible, roll-up-sleeves attitude, self-directed and willing to travel frequently.
  • Keen interest in scientific and technical issues related to clinical study.
  • Ability to work and collaborate effectively with internal and external actors to achieve company objectives.
  • Excellent oral and written communication skills in English. Any other language is a plus.
  • Up to 30% travel may be required.
Offer:
  • A challenging position with a high potential innovative medical device company.
  • To work in a human-sized, collaborative and respectful environment
  • A variety of interesting contacts with international exposure.
  • An attractive compensation package in line with the position’s responsibilities and your experience.

Scientific Communication & Marketing Officer - Medical Device - Gosselies

Founded in 2005, Graftys develops, manufactures and markets patented synthetic bone biomaterials for reconstructive orthopedic surgery. Graftys is specialized in new generations of resorbable calcium-phosphate cements and is based on the research works of Pr. Jean-Michel Bouler (CEISAM/CNRS). 

The Company’s key products are commercialized in more than 25 countries, including Europe and the USA, through distribution partnerships. The objective of Graftys is to expand the company product lines by offering new versions of existing products and new products with enhanced regenerative properties.

Graftys, one of the world leaders in resorbable bone cements, is based in Belgium and France. For more information about the company, please visit https://www.graftys.com 

In order to support the expansion of the dynamic team in Gosselies, we are looking for a (m/f):

Scientific Communication & Marketing Officer

Responsibilities:

As a Scientific Communication & Marketing Officer, you are the scientific referent of the marketing and sales department. You support new market/customer development and fuel existing partners.

Your main responsibilities are as follows:

  • You organize and ensure scientific and technological watch (clinical & lab data) and propose digital optimization models.
  • You write and help writing scientific, clinical or white papers including scientific and clinical data collection.
  • You build the scientific communication of the products (characteristics, performances …).
  • You ensure training to practitioners and distributors internationally.
  • You are the interface with and answer technical questions from customers/partners.
  • You represent Graftys at conferences, workshops and meetings internationally.
  • You provide internal scientific communication and training.
  • You are the link between the departments of the company (e.g., Clinical & Regulatory – PMS, clinical data, R&D department -pipeline and publication program…).
Profile:
  • You hold a master’s degree in biomedical sciences, chemistry, pharmacy, etc.; a PhD is a plus.
  • You have at least 3 years’ experience in medical writing and/or scientific marketing communication, ideally in the implantable medical device, biotech or pharma industry.
  • You show excellent oral and written communication skills and strong interpersonal skills.
  • You demonstrate a good sense of organization, responsibility and flexibility.
  • You are motivated, proactive, curious and attentive to new trends and technologies in the Graftys’ sector.
  • You are fluent in French and English, written and spoken. Knowledge of another language is an asset.
Offer:
  • A challenging and rewarding position within a fast-growing company.
  • The opportunity to join a company specialized in innovative product for reconstructive orthopedic surgery.
  • To work in a human-sized, innovative, collaborative and dynamic company.
  • An attractive salary package in line with your experience.

Clinical Study Manager - Medical Device - Gosselies

Founded in 2005, Graftys develops, manufactures and markets patented synthetic bone biomaterials for reconstructive orthopedic surgery. Graftys is specialized in new generations of resorbable calcium-phosphate cements and is based on the research works of Pr. Jean-Michel Bouler (CEISAM/CNRS).

 The Company’s key products are commercialized in more than 25 countries, including Europe and the USA, through distribution partnerships. The objective of Graftys is to expand the company product lines by offering new versions of existing products and new products with enhanced regenerative properties.

Graftys, one of the world leaders in resorbable bone cements, is based in Belgium and France. For more information about the company, please visit www.graftys.com.

In order to support the expansion of the dynamic team in Gosselies, we are looking for a (m/f):

Clinical Study Manager

Responsibilities:

As a Clinical Study Manager, you lead and coordinate clinical trials (phases I, II and III) from study design and protocol development to the study close-out and clinical data review.

Your main responsibilities are as follows:

  • You manage and coordinate clinical trials of phases I, II and III and/or medical device equivalents.
  • You participate to study design and protocol development.
  • You deal with the medical writing of study related documents: protocols, IB, ICF, CRF…
  • You prepare regulatory documents and submission files to EC and CA.
  • You manage site relationships: investigators, site selection, initiation visits, investigator agreement preparation, organization of investigator/meetings, monitoring activities
  • You ensure the review of clinical trial data, support in preparation of clinical study reports
  • You manage vendors.
  • You review medical literature and related new technologies, and close collaboration with other departments: preclinical, regulatory, production, QC, IP…
Profile:
  • You hold an advanced scientific degree: PhD, DVM, MD.
  • You have at least 5 years’ experience in clinical operations, ideally in the implantable medical device or in the biotech industry.
  • You have good knowledge of ISO & GCP-ICH principles.
  • You show excellent oral and written communication skills and strong interpersonal skills.
  • You demonstrate a good sense of organization, responsibility and flexibility.
  • You are fluent in French and English, written and spoken. Knowledge of another language is an asset.
Offer:
  • A challenging and rewarding position within a fast-growing company.
  • The opportunity to join a company specialized in innovative product for reconstructive orthopedics.
  • To work in a human-sized, innovative, collaborative and dynamic company.
  • A full-time permanent contract (CDI) with an attractive salary package in line with your experience.

Network & Security Engineer and Architect - IT & Consultancy Solutions - Louvain-la-Neuve

Fondée en 2015, PROCSIMA-GROUP est une entreprise spécialisée en sécurité informatique. PROCSIMA-GROUP aide les entreprises à protéger leurs informations et leurs données contre les attaques externes et internes de toute nature, et à assurer la bonne performance de leurs systèmes ainsi que la bonne disponibilité de leurs services.

Située à Louvain-la-Neuve et composée d’une quinzaine de consultants, PROCSIMA-GROUP vise à devenir le leader belge de la cyber protection en fournissant des services, de la consultance et des solutions à haute valeur ajoutée, tels que : services d’audit & reviews, protection des données, stratégie, architecture, gouvernance, GDPR, etc.

Pour de plus amples informations, veuillez consulter http://www.procsima-group.eu.

Afin de renforcer l’équipe, nous sommes activement à la recherche (CDI ou freelance) d’un(e) :

Network & Security Engineer and Architect

 Responsabilités :

En tant que Network & Security Engineer and Architect, vos principales responsabilités sont les suivantes :

  • Réaliser des audits et études de robustesse et d’architecture du réseau et de la sécurité mise en place chez les clients, notamment via des tests d’intrusion et de pénétration.
  • Conseiller le client en fournissant des recommandations concrètes.
  • Proposer au client une feuille de route et une stratégie à court, moyen et long terme.
  • Accompagner le client dans ses projets d’amélioration et à la mise en place de la stratégie.
  • Participer à des projets en tant qu’ingénieur spécialisé en réseau et sécurité, et en tant qu’architecte de sécurité.
  • Créer les designs avec méthode et conseiller les équipes projets et opérationnelles.
  • Participer à la gestion et à l’amélioration des services de sécurité des réseaux de PROCSIMA-GROUP.
Profil :
  • Vous disposez idéalement de 3 à 5 ans d’expérience dans une position similaire. Les profils juniors sont également les bienvenus.
  • Vous maitrisez le design des architectures réseau.
  • Vous possédez une bonne connaissance générale des firewalls les plus utilisés (Palo Alto, Checkpoint, Fortinet, F5, etc.) et des proxys, reverse proxys et autres équipements (Bluecoat, etc.).
  • Vous avez des notions de gestion de projet (Prince2 ou PMI), et avez une bonne connaissance des systèmes de gouvernance ITIL et CobiT. Une certification réseau Cisco, Ethical Hacking ou en cybersécurité est un sérieux atout.
  • Vous êtes pragmatique, organisé(e), autonome, et doté(e) d’un bon esprit d’analyse et de synthèse.
  • Vous faites preuve d’un esprit d’équipe développé et avez de bonnes compétences communicationnelles et d’écoute.
  • Vous communiquez aisément en français. La connaissance de l’anglais/néerlandais est un atout.
  • Vous êtes disposé(e) à vous déplacer en fonction des missions (Bruxelles, Wallonie).
Offre :
  • Intégrer une entreprise en pleine croissance proposant des solutions innovantes et variées.
  • Une fonction challengeante et diversifiée dans un secteur en plein développement.
  • L’opportunité de travailler sur divers projets pour le compte de différents clients.
  • La possibilité de travailler sous contrat à durée indéterminée ou en tant que freelance.
  • Une offre salariale attrayante, assortie d’avantages extralégaux compétitifs en phase avec votre expérience.
  • Un plan de formation en adéquation avec des objectifs de développement clairs.

Expert Qualité Produit - Aéronautique - Sars-et-Rosières

Née d’un projet industriel commun de deux leaders mondiaux de l’industrie aéronautique, Air France Industries KLM E&M et Safran Aircraft Engines, Airfoils Advanced Solutions est une usine 4.0 mettant en œuvre des hautes technologies dans ses procédés industriels et dans ses systèmes d’information. Ce site unique en Europe est dédié à la réparation d’aubes de compresseurs haute-pression de moteurs d’avions de ligne (GE90, CFM56, GP7200).

Implantée sur le Parc d’Activités de Sars-et-Rosières, à 25 min de Lille, Airfoils Advanced Solutions emploie actuellement 50 personnes, avec l’objecitf d’atteindre le cap des 200 employés à l’horizon 2022.

Afin de renforcer son équipe, nous sommes activement à la recherche d’un (h/f) :

Expert Qualité Produit

Responsabilités :

En tant qu’Expert Qualité Produit, vous assurez aux clients de l’entreprise des produits et services de classe mondiale en termes de sécurité, de qualité, de fiabilité et de performance. Rapportant au Responsable Qualité & Sécurité, vous contribuez au développement de la culture qualité et sécurité de l’entreprise.

Vos principales responsabilités sont :

  • Mettre en place les indicateurs, les outils qualité et les procédures de contrôle appropriées.
  • Coordonner les moyens de suivi de la qualité des produits livrés aux clients et de leur conformité pendant les phases d’industrialisation et de production.
  • Assurer l’amélioration continue de la qualité du produit, collecter les problématiques produit/process rencontrées et suggérer des recommandations pour améliorer les instructions et la qualité du produit.
  • Organiser un programme de surveillance (Sondages, Self audits) en vue de vérifier la conformité des produits aux procédures en vigueurs.
  • Être le garant du respect des exigences réglementaires internes/externes et des spécifications normatives applicables.
  • Animer, promouvoir et garantir le respect de la politique Qualité et Sécurité de l’entreprise pour assurer la confiance des clients.
  • Organiser des actions de sensibilisation et de formation du personnel aux problèmes de la qualité.
Profil :
  • Vous possédez 10 ans d’expérience dans les technologies industrielles, telles que la fabrication et/ou la réparation de pièces de moteurs d’avion. A ce titre, vous avez acquis de solides compétences techniques liées aux activités de la maintenance moteurs d’avions.
  • Vous démontrez de bonnes connaissances des activités relatives à la qualité produit/process ainsi qu’une maitrise des outils de qualité (8D ; AMDEC, PDCA, audit,…).
  • Vous disposez d’une réelle aisance relationnelle.
  • Vous appréciez le travail en équipe et êtes capable de mobiliser et fédérer.
  • Vous êtes organisé(e), analytique et faites preuves de bonnes capacités de synthèse et rédactionnelles.
  • Vous êtes disposé(e) à vous déplacer en France.
  • Vous communiquez aisément en français et en anglais.
Offre :
  • Une fonction diversifiée incluant des projets intéressants.
  • Intégrer un site unique en Europe à la pointe du développement.
  • Un salaire attractif assorti d’avantages extra-légaux, en phase avec votre expérience.
  • Un contrat à durée indéterminée à temps plein.