41 Emplois pour Process Improvement - France

Join 3C Metal: A Global Leader in Turnkey Project Solutions!

Are you ready to join a dynamic team driving innovation in engineering?

Established in 1995, 3C Metal Group started as a specialist in high-pressure piping, welding, and installation services for the oil and gas sector. Over the years, the company has diversified its expertise into renewable energy, green technology, power generation, marine, and mining industries. Today, 3C Metal Group is present in eight countries across four continents and has a workforce of 1,000 employees. In 2024, 3C Metal Group joined the Ortec Group, further enhancing our capabilities and expanding our global presence.

As part of this global network, the Namibia location, based in Walvis Bay, specializes in engineering, fabrication and construction, project management, onsite installation, procurement, and laser scanning. The recent oil discovery in Namibia opens up prospects for economic growth, job creation, and a transformative energy future—and 3C Metal Belmet is proud to be part of this exciting journey. Our mission is to provide efficient and competitive solutions for retrofit and upgrade projects for the energy industry worldwide to become the market leader for turnkey project solutions.

Why Choose 3C Metal?

• Global footprint: Originating in France, 3C Metal has expanded its presence to the USA, Namibia, South Africa, Mozambique, the UAE, and Malaysia, offering a truly international experience.
• Innovation & Expertise: We pride ourselves on our ability to deliver exceptional results through cutting-edge technologies, design solutions, and world-class project management.

As part of our Quality team, you will play a crucial role in ensuring the successful delivery of engineering solutions for complex projects. You will be responsible for the full coordination of quality control for 3C Metal Belmet.

Your responsibilities will include:

• Ensuring sufficient coverage for all QC requirements across all projects without hindering production progress.
• Implementing and adhering to code requirements across standard workshop activities without deviation.
• Reviewing and implementing specific client requirements without deviation.
• Providing technical support and guidance to the production team.
• Training and developing QC Inspector trainees.
• Ensuring ISO 9001 compliance.

Quality Control Technician (CDI)

Company Overview

Kimialys is an innovative industrial company specializing in in vitro analysis, with applications centered around K-One, a patented surface treatment technology developed over a decade at ENS Paris-Saclay. Our mission: enabling the development of tomorrow’s diagnostics and therapeutics.

The company comprises fifteen employees, including ten chemists and engineers specialized in biosensors. Our clients include developers of rapid and point-of-care diagnostic tests as well as pharmaceutical laboratories in the drug discovery and clinical development phases.

Responsibilities

1. Performing physicochemical analyses of raw materials, reaction intermediates, and finished products;
2. Verifying results against specifications and completing qualification/validation documents;
3. Preparing quality control reports and certificates of conformity for each production batch;
4. Calibrating and maintaining production and R&D equipment;
5. Complying with HSE guidelines, procedures, and the existing quality system;
6. Ensuring the production of reaction intermediates.

Note that the above list is not exhaustive and may be supplemented based on activity or Kimialys' strategy.

Qualifications

1. Graduate with a 2-year or 3-year degree in Biophysics, including Quality Control;
2. First experience in physico-chemical characterizations for quality control would be highly appreciated;
3. Background in nanomaterial characterization would be a plus (UV-vis, DLS, Zeta Potential, TEM), but not required.

Required Skills & Qualities

1. Rigor, critical thinking, autonomy, and proactivity will be essential qualities for this position;
2. Ability to collaborate effectively within a team and good communication skills;
3. High adaptability and flexibility to navigate in a dynamic environment;
4. Capacity to take initiatives for the continuous improvement of our processes;
5. Professional English proficiency, both written and spoken.

Why Join Kimialys?

1. Be part of a human journey where excellence and conviviality coexist;
2. Have the chance to work with some of the most innovative companies in the life science industry worldwide, developing tomorrow’s diagnostics and therapeutics;
3. Enjoy working in the heart of Paris, within the Cochin hospital campus.

Interested in the position? Contact us at Thank you for your interest!

À partir d'un dossier de fabrication et d'une gamme de contrôle / Fiche d'enregistrement de contrôle :
•Contrôler 1ère pièce des séries en usinage (dimensionnel, visuel et fonctionnel)
•Contrôler dimensionnel, visuel et fonctionnel des pièces en cours de fabrication et en contrôle final
•Contrôle documentaire des éléments du dossier de fabrication (cohérence et conformité des résultats sur les fiches d'autocontrôle par exemple, l'ordre de fabrication.)
•Enregistrer les résultats des contrôles sur une fiche d’enregistrement de contrôle (FEC)
•Déclencher et saisir les fiches de non-conformité dans l'outils qualité. Solliciter l'appui technique de son n+1
•Utiliser les programmes de contrôle sur les machines de contrôle spécifique adapté

Company Overview:

MACOM designs and manufactures semiconductor products for Data Center, Telecommunication and Industrial and Defense applications. Headquartered in Lowell, Massachusetts, MACOM has design centers and sales offices throughout North America, Europe, and Asia. MACOM is certified to the ISO9001 international quality standard and ISO14001 environmental management standard.

MACOM has more than 65 years of application expertise with multiple design centers, Si, GaAs and InP fabrication, manufacturing, assembly and test, and operational facilities throughout North America, Europe, and Asia. In addition, MACOM offers foundry services that represent a key core competency within our business.

MACOM sells and distributes products globally via a sales channel comprised of a direct field sales force, authorized sales representatives, and leading industry distributors. Our sales team is trained across all of our products to give our customers insights into our entire portfolio.

MACOM is an Equal Opportunity Employer committed to a diverse workforce. MACOM will not discriminate against any worker or job applicant on the basis of race, color, religion, gender, gender identity, gender expression, national origin, ancestry, age, sexual orientation, marital or civil partnership status, pregnancy, disability, genetic information, veteran status, military obligations, or membership in any other category protected under applicable law.

Role Purpose:

The Quality Control & Back-end Inspector will perform manual or semi-automatic sampling, visual inspections, and packaging of MMIC circuits and finished wafers within the required time and in accordance with specifications.

Main Duties and Responsibilities:

1. Perform incoming inspection, in-process inspection, first article inspection, and final inspection of electronic and mechanical components with little to no assistance.
2. Schedule source inspections as required.
3. Generate internal and external reports.
4. Generate and maintain data for the control of documentation, effectively report information, and accurately respond to questions from team members, internal suppliers, and customers.
5. Communicate non-conformances and work with Quality and Manufacturing to drive corrective actions. Ensure all incoming, in-process, and final materials meet specifications.
6. Perform routine SAP transactions to move, disposition, and route material.

Key Competencies Required:

1. Quick-thinking, self-motivated individual with knowledge on all aspects of inspection and testing.
2. Experience with Mil-STD-883 2010.
3. Knowledge and experience in performing mechanical and electronic inspection.
4. Ability to work from technical drawings, sketches, and specifications.
5. Safe handling of ESD sensitive materials.
6. Working knowledge of SAP, Agile, Excel, MSWord, and Outlook.
7. Good communication skills are important, as well as the ability to explain findings clearly.
8. Good report writing skills.
9. Fluent in French.

Previous Relevant Work Experience:

1. Minimum 1 year Quality Control inspection experience preferred.

Minimum Qualifications:

1. Higher education (BAC +2) or a professional license in the scientific or technical field or have experience in the field of industrial quality control.
2. Basic understanding of quality control standards and testing techniques.
3. Intermediate level in English.

Join to apply for the Quality Control Inspector role at Stryker

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Join to apply for the Quality Control Inspector role at Stryker

Responsibilities include:

• Controlling the first piece of machining series (dimensional, visual, and functional checks)
• Dimensional, visual, and functional control of parts during manufacturing and final inspection
• Document control of manufacturing records (coherence and conformity of results on self-control sheets, manufacturing order, etc.)
• Recording control results on a control record sheet (FEC)
• Triggering and entering non-conformity reports in the quality tool; seeking technical support from supervisor
• Using control programs on specific control machines

Stryker is a global leader in medical technologies, committed to improving healthcare outcomes through innovative products and services in MedSurg, Neurotechnology, Orthopaedics, and Spine. The company impacts over 150 million patients annually worldwide.

• Entry level

• Full-time

• Quality Assurance

• Medical Equipment Manufacturing, Appliances, Electrical and Electronics Manufacturing, Industrial Machinery Manufacturing

Referrals increase your chances of interviewing at Stryker by 2x.

MACOM is an Equal Opportunity Employer committed to a diverse workforce. MACOM will not discriminate against any worker or job applicant on the basis of race, color, religion, gender, gender identity, gender expression, national origin, ancestry, age, sexual orientation, marital or civil partnership status, pregnancy, disability, genetic information, veteran status, military obligations, or membership in any other category protected under applicable law.

Role Purpose :

The Quality Control & Back-end Inspector will perform manual or semi-automatic sampling, visual inspections and packaging of MMIC circuits and finished wafers within the required time and in accordance with specifications

Main Duties and Responsibilities :

• Perform incoming inspection, in-process inspection, first article inspection and final inspection of electronic and mechanical components with little to no assistance
• Schedule source inspections as required
• Generate internal and external reports
• Generate and maintain data for the control of documentation, effectively report information, and accurately respond to questions from team members, internal suppliers, and customers
• Communicate non-conformances and work with Quality and Manufacturing to drive corrective actions. Ensure all incoming, in-process and final materials meet specifications
• Perform routine SAP transactions to move, disposition, and route material
• Quick-thinking, self-motivated individual with knowledge on all aspects of inspection and testing
• Experience with Mil-STD-883 2010
• Knowledge and experience in performing mechanical and electronic inspection
• Ability to work from technical drawings, sketches and specifications
• Safe handling of ESD sensitive materials
• Working knowledge of SAP, Agile, Excel, MSWord and Outlook
• Good communication skills are important, as well as the ability to explain findings clearly
• Good report writing skills
• Fluent in French
• Minimum 1 year Quality Control inspection experience preferred.

Minimum Qualifications :

• Higher education (BAC +2) or a professional license in the scientific or technical field or have experience in the field of industrial quality control.
• Basic understanding of quality control standards and testing techniques.

Quality Control Inspector • Paris, IDF, FR

Vous assurez le support analytique pour les activités de contrôle qualité et de développement analytique sous-traitées, dans un environnement conforme aux exigences GxP.

Vous gérez des projets analytiques en collaboration avec des équipes externes telles que des CMO/CDMO et des laboratoires analytiques.

• Revoir et valider la conception des protocoles analytiques (développement / transfert / validation.) ainsi que le contenu des rapports associés.

• Gérer les événements qualité externes chez les CMO/CDMO et dans les laboratoires analytiques (OOS, déviation, change control, CAPA…) liés aux activités analytiques.

• Gérer les événements qualité internes (déviation, change control, CAPA…) liés au Contrôle Qualité.

• Contribuer de manière transversale avec les équipes de DBV aux projets de développement de nouveaux produits (volet analytique).

• Relecture des dossiers d’enregistrement (IND, IMPD, BLA.) et contribution aux réponses aux autorités.

• Mise à jour des QTA (partie Contrôle Qualité).

• Réaliser des audits internes et externes.

• Rédiger et mettre à jour les procédures internes / documents de travail du département Contrôle Qualité.

• Participer à la rédaction / mise à jour des spécifications produits / matières.

• Gérer les standards analytiques avec les partenaires de DBV : stratégie par standard, stock, renouvellement, stabilité, études spécifiques.

• Assister le Référent Standards dans les activités associées.

• Gérer le budget des activités sous sa responsabilité.

Profil :

• Diplôme d'ingénieur, master ou doctorat en sciences analytiques (pharmacie, biochimie, physico-chimie, biologie…).

• Expérience en Contrôle Qualité de produits pharmaceutiques et en environnement BPF (Bonnes Pratiques de Fabrication).

5 ans d'expériences

Compétences :

• Maîtrise des méthodes biochimiques et des techniques analytiques adaptées aux macromolécules (et plus particulièrement aux protéines) (SDS-PAGE, ELISA, Bradford, WESTERN BLOT, HPLC…).

• Connaissance des lignes directrices et normes applicables dans l’industrie pharmaceutique (BPF, ICH…).

• Expérience en développement, validation et transfert de méthodes analytiques.

• Expérience en gestion des standards de référence.

• Connaissance des outils Microsoft Office (Word et Excel).

• Niveau d’anglais : lecture, écriture, expression orale.

Compétences comportementales :

• Curiosité : Désir démontré d'apprendre, d'explorer et de comprendre de nouvelles choses.
• Courage : Capacité à affronter la peur, l'incertitude et les défis avec confiance et détermination.
• Collaboration : Travailler avec les autres pour atteindre un objectif commun.
• Crédibilité : Construit la confiance, est fiable, agit avec éthique et intégrité.

Our partner embodies excellence in the field of food processing. With a rich history and a steadfast commitment to quality, they have established an excellent reputation. Today, they are opening their doors to a talented professional who will join their team as Quality Control Technician. Under the direction of their Quality Coordinator, you will have the opportunity to contribute to their legacy by performing a diverse range of essential tasks. Your contribution will play a crucial role in their ongoing commitment to excellence and customer satisfaction.

1. Conducting pre-operational inspections to ensure equipment compliance before the start of operations.
2. Performing verifications and analyses throughout the manufacturing process according to established protocols.
3. Evaluating incoming raw materials based on established quality criteria.
4. Participating in the development and implementation of quality control plans.
5. Ensuring compliance with Good Manufacturing Practices (GMP) and food safety standards.
6. Training new employees (GMP).
7. Maintaining and updating quality control-related documents.
8. Collaborating closely with production teams to resolve quality issues.
9. Performing all related tasks.

1. Group insurance.
2. Job stability.
3. Joining a dynamic and engaging team.
4. On-site parking.
5. Work-life balance.
6. Family-owned company that has been growing since 1937.

1. DCS in Dietetic Techniques (preferred), Food Processing, or other relevant education/experience.
2. Ideally, 1 year of experience in a similar quality control role in a manufacturing environment.
3. Proficiency in French, both spoken and written.

1. Ability to walk several hours a day in the factory, demonstrating resilience and physical endurance.
2. Ability to make informed and quick decisions in variable situations.
3. Attention to detail and precision in task execution, ensuring strict adherence to quality and food safety standards.

Role Definition

Context

The Project team is responsible for the successful execution of projects with maximum customer satisfaction. It is spread across several locations.

Depending on the project scope, contract requirements, complexity, or individual competence, the Quality Engineer may also be assigned temporarily as a Project Health & Safety Manager or Project Environmental Manager. See separate Job Descriptions for these areas of responsibility.

Purpose

Manage all aspects of Quality in project execution and during the Tender phase when required.

Ensure that Nexans’ Management system, procedures, and Client’s requirements and expectations are met.

Ensure the project team is knowledgeable about and compliant with G&T Management systems and tools.

Assist in the continuous improvement of the organization regarding Quality activities.

Areas of responsibility

General Description

As the Project Quality Manager, manage the required Quality activities for the project by preparing and communicating the relevant Project Plans and Procedures from project start-up to close-out, in compliance with the project model requirements.

Specific Descriptions

• Assist the Project Team in meeting their day-to-day responsibilities for Quality performance.
• Ensure effective coordination and communication with Plant Quality, Land, and Marine Installation project teams related to Quality assurance activities.
• Coordinate with the Client on Quality topics.
• Establish the Project Quality Plan as per template and monitor compliance.
• Manage and distribute specific project KPIs related to Quality.
• Develop Inspection & Test Plans, establish the Project Inspection and Test Plan as per process and template, and ensure activities are performed according to the QS Plan.
• Plan, notify, and coordinate with Clients on applicable R, W, and H points from the project ITP (not applicable for Nx own Manufacturing).
• Organize project document reviews and manage customer comments and document revisions until full approval.
• Establish Final Documentation Index file and follow-up on completeness and status; coordinate collection of Quality documents.
• Establish Project Compliance report and organize review meetings; monitor compliance with Project Model Stage Gates.
• Ensure thorough review and approval of changes impacting the project execution.
• Manage Non-Conformance Reporting, concessions, and deviations.
• Support the FMEA process when required.
• Assist and coordinate Client, Supplier, and Subcontractor Audits.
• Facilitate Lessons Learned processes.
• In tender, analyze Quality demands and provide input to the Tender Manager.

Expected results

• Ensure project execution complies with contract quality requirements, Nexans G&T standards, and regulatory environment.
• Develop preventive actions to reduce non-quality costs and non-conformances.
• Mitigate risks with appropriate measures.
• Use quality assurance planning tools effectively to meet Quality targets.

Requested Competencies and Qualifications

• Supporting Senior or Specialist Project Quality Managers, with some understanding of Quality within Nexans projects.
• 0-4 years of experience as Quality Manager from manufacturing, installation, or offshore sectors.
• Skilled in Project Management and methods.
• Understanding of project-driven organizations and requirements.
• Trained and certified in Quality and Risk Management.
• University degree (MSc, MBA, BSc or similar), preferably in engineering or QHSER discipline.
• Knowledge of industrial processes such as cable manufacturing, relevant industry, and marine/land installation works.
• Fluent in English, both verbal and written.