Empowered by purpose.
Qualité et réglementation chez Bio-Rad
Nos équipes qualité, affaires réglementaires et cliniques jouent un rôle essentiel en aidant Bio-Rad à respecter ses engagements de longue date en matière de qualité, d'innovation et d'excellence opérationnelle. En répondant aux exigences des clients et de la réglementation et en favorisant une culture d'amélioration continue et durable, nous aidons Bio-Rad à fournir des produits sûrs et efficaces qui font progresser la science et améliorent la santé humaine.
Les employés de Bio-Rad issus de différentes équipes partagent ce qu'ils apprécient le plus dans la culture de travail de Bio-Rad.
Jennifer explique comment la culture collaborative chez Bio-Rad l'a aidée à développer sa carrière et à développer des produits de haute qualité.
Emplois Qualité et Réglementation
| Titre | Importance Du Travail | Type De Travail | Entité Légale | Niveau D'expérience | Subscribe To Alerts | Identificateur de réquisition | Ville | Etat | Pays | Emplacement | Département | Catégorie | Sommaire | Type d'emploi | Niveau |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Quality Engineer I - Temporary | Hybride | Niveau d'entrée | 2025-36485 | Hercules | California | United States | Hercules, California, United States | Qualité et réglementation | The Quality Engineer will help facilitate the updating and consolidation of legacy product risk management files related to IVDR. How You'll Make An Impact: Facilitating risk management assessments, updating risk plans and reports, consolid... | ||||||
| Technical Writer III | Hybride | (USA_1000)Bio-Rad Laboratories, Inc. | Niveau intermédiaire | 2025-36548 | Irvine | California | United States | Irvine, California, United States | Qualité et réglementation | As the Technical Writer III, you will provide technical writing for medical device and in vitro diagnostic products to ensure regulatory compliance and customer expectations are met, including but not limited to technical documentations, regulator... | |||||
| QC Specialist III | Essentiel (sur place) | (USA_1000)Bio-Rad Laboratories, Inc. | Niveau intermédiaire | 2025-36517 | Irvine | California | United States | Irvine, California, United States | Qualité et réglementation | As a QC Specialist III, you will operate, maintain, and troubleshoot QC Laboratory instrumentation. Create and release product batch records according to applicable procedures.Evaluate assay runs for accuracy and input data into the appropriate da... | |||||
| QC Technician II | Essentiel (sur place) | (USA_1000)Bio-Rad Laboratories, Inc. | Niveau intermédiaire | 2025-36518 | Irvine | California | United States | Irvine, California, United States | Qualité et réglementation | In this role as a QC Technician II, you will support the testing and documentation needs of the Quality Control department during the manufacture and release of Bio-Rad control products. This position will work both independently and in a team-ori... | |||||
| Quality Systems Specialist - Temporary | Hybride | Niveau d'entrée | 2025-36506 | Irvine | California | United States | Irvine, California, United States | Qualité et réglementation | This position will support the compilation and maintenance of IVDR technical files, review IVDR and other registration labeling change requests and various quality tasks to support the QMS overall. How You'll Make An Impact: Review, approve,... | ||||||
| Spécialiste Assurance Qualité CDD | Hybride | (FRA_2018)Bio-Rad | Cadre supérieur / Responsable | 2025-36456 | MARNES-LA-COQUETTE | France | MARNES-LA-COQUETTE, France | Qualité et réglementation | Vous voulez participer à la qualité de produits qui favorisent la découverte scientifique et contribuent à améliorer la vie des patients ? Vous souhaitez rejoindre une entreprise d’envergure internationale ? Alors, rejoignez-nous et devenez no... | ||||||
| Supplier Quality Manager | Hybride | (USA_1000)Bio-Rad Laboratories, Inc. | Cadre supérieur / Responsable | 2025-36473 | Hercules | California | United States | Hercules, California, United States | Qualité et réglementation | As a Regional Supplier Quality Manager, the candidate plays a key leadership role overseeing supplier quality and compliance activities across the region. Their day involves collaborating with a team of Supplier Quality Engineers to drive performa... | |||||
| Lead Auditor | à distance | (USA_1000)Bio-Rad Laboratories, Inc. | Niveau intermédiaire | 2025-36432 | Seattle | Washington | United States | Seattle, Washington, United States | Qualité et réglementation | Support Bio-Rad's commitment to quality and compliance by coordinating the internal and external audits as a Lead Auditor/Audit Coordinator. As part of Bio-Rad's Seattle Operations Regulatory Affairs team, you’ll apply your strong leadership skill... | |||||
| Regulatory Affairs Specialist II - Temporary | Hybride | Niveau intermédiaire | 2025-36484 | Irvine | California | United States | Irvine, California, United States | Qualité et réglementation | Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all Bio-Rad products currently CE Marked under the IVD Directive. Activities include preparation revision of technical files when needed, update labelin... | ||||||
| Design Quality Engineer | Hybride | (USA_1000)Bio-Rad Laboratories, Inc. | Niveau intermédiaire | 2025-36477 | Irvine | California | United States | Irvine, California, United States | Qualité et réglementation | The Bio-Rad Laboratories Design Quality Assurance team located in Irvine, CA, is seeking a detail oriented Design Quality Engineer to support the design, development and maintenance of life science and clinical diagnostics products. You will work... | |||||
| Quality Sys Spec I | Hybride | (SGP_3001)Bio-Rad Laboratories - Commercial Singapore | Niveau d'entrée | 2025-36457 | Singapore | Singapore | Singapore | Qualité et réglementation | The successful incumbent will : Support ISO 13485:2016, ISO 9001:2015, SS620: 2016 or equivalent for Singapore Distribution Center (Asia Pacific and South East Asia) Support internal Audits Identifies gaps in compliance and takes necessary ac... | ||||||
| Regulatory Affairs Manager | Hybride | (HUN_2035)Bio-Rad Hungary Trading LLC | Cadre supérieur / Responsable | 2025-36449 | Budapest | Hungary | Budapest, Hungary | Qualité et réglementation | The Regulatory Affairs Manager will be responsible for the development, implementation, and on-going improvement of programs in the areas of regulatory compliance, document control, and product registrations/ submissions for the products manufactu... | ||||||
| QC Tech I - Temporary | Essentiel (sur place) | Niveau d'entrée | 2025-36468 | Hercules | California | United States | Hercules, California, United States | Qualité et réglementation | The QC Tech will start the day by printing all the necessary SOP’s for pending QC inspections for incoming raw materials, semi-finished and finished goods. After training is completed, they will inspect these incoming materials (i.e. labels, raw m... | ||||||
| Quality Sys Spec I (fixed term 12 months) | Hybride | (SGP_3001)Bio-Rad Laboratories - Commercial Singapore | Niveau d'entrée | 2025-35984 | Singapore | Singapore | Singapore | Qualité et réglementation | Primary Role: The Quality System Specialist (Fixed Term) supports the Quality Management System (QMS) implementation and maintenance in alignment with ISO 9001:2015, SS620:2016, ISO 13485, and GDPMDS requirements. This role is pivotal in ensur... | ||||||
| Quality System Specialist | Hybride | (HUN_2035)Bio-Rad Hungary Trading LLC | Cadre supérieur / Responsable | 2025-36258 | Budapest | Hungary | Budapest, Hungary | Qualité et réglementation | In alignment with Global RA/QA strategic aims, this position manages the Quality Management System for Budapest to ensure the QMS is maintained in compliance with all applicable quality and regulatory requirements. Our new colleague will promote b... | ||||||
| Regulatory Affairs (RA) Specialist | Hybride | (AUS_3012)Bio-Rad Laboratories Pty Ltd | Niveau intermédiaire | 2025-36383 | Sydney | Australia | Sydney, Australia | Qualité et réglementation | A key member of the Regulatory Affairs Function, accountable for providing regulatory affairs knowledge and support the business meeting its objectives, as well as regional RA activities. Delivering product pre market approval within the timefram... | ||||||
| Quality System Specialist III | Essentiel (sur place) | (USA_1000)Bio-Rad Laboratories, Inc. | Niveau intermédiaire | 2025-36102 | Irvine | California | United States | Irvine, California, United States | Qualité et réglementation | The Bio-Rad Irvine Distribution Center requires a dedicated Quality System Specialist position to provide the leadership and direction needed to support Global Logistics operations at the facilities including regulatory compliance and the developm... | |||||
| Quality System Specialist III | Essentiel (sur place) | (USA_1000)Bio-Rad Laboratories, Inc. | Niveau intermédiaire | 2025-36080 | Richmond | California | United States | Richmond, California, United States | Qualité et réglementation | The Bio-Rad Richmond Distribution Center requires a dedicated Quality Systems Specialist to provide the guidance and direction needed to support Global Logistics operations at the facilities including regulatory compliance and the development, imp... | |||||
| QC Supervisor II (Second Shift) | Hot Job | Essentiel (sur place) | (USA_1000)Bio-Rad Laboratories, Inc. | Niveau intermédiaire | 2024-35731.1 | Irvine | California | United States | Irvine, California, United States | Qualité et réglementation | As the Bio-Rad QC Supervisor, you will oversee the day to day responsibilities around the testing and release of manufactured material. You will interface with multiple departments to achieve product release timelines. Maintain high levels of qual... | ||||
| BSA, Sr | Hybride | (IND_3006)Bio-Rad Laboratories (India) Pvt Ltd | Niveau intermédiaire | 2025-36265 | Remote | India | Remote, India | Qualité et réglementation | As part of the Global IT Team, this position will lead the harmonization of Quality Management System (QMS) solutions, from a technology perspective, and the implementation and stabilization of Veeva Vault as a global eQMS software solution, worki... | ||||||
| RA Mgr I | Essentiel (sur place) | (TWN_3016)Taiwan Branch of Bio-Rad Laboratories, Inc. | Niveau intermédiaire | 2025-36164 | Taipei | Taiwan | Taipei, Taiwan | Qualité et réglementation | Organize RA activities and local QA work to ensure the operation of the company is in compliance with local FDA and other related authorities’ requirements How You’ll Make an Impact: Product registration, including new registration, rene... |
Impact significatif
Nous partageons la même volonté de repousser les limites de la science et d'aider les gens du monde entier à vivre plus longtemps et en meilleure santé. Cette mission, à laquelle nous travaillons tous chaque jour, guide notre travail et dynamise nos équipes dans le monde entier
Expérience employé
Collaborez et innovez avec vos collègues pour obtenir des résultats et transformer la façon dont nous relevons les défis, tout en travaillant au sein d'une équipe mondiale qui s'encourage mutuellement à faire mieux chaque jour.
Développement de carrière
Notre tradition est de développer des parcours professionnel ayant un but et un impact et cela commence par vous donner les outils, les expériences et la flexibilité nécessaires pour suivre un parcours qui soutient vos ambitions actuelles et futures. Profitez de la liberté de prendre des risques et de contribuer à transformer l'avenir de l'entreprise et de votre carrière.
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