Caring for the world … one person at a time inspires and unites the people of Johnson & Johnson. This culture of caring is the focus of our corporate philosophy, that is anchored in the internationally applicable Credo. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.Main ResponsibilitiesAccountable for administration of the Change Order (CO) process.Accountable for compliance with the Food and Drug Administration's (FDA) Quality System Regulation (QSR) as it pertains to Documentation and Documentation Control.Accountable for the timely processing and release of new and changed controlled documents.Accountable that all Change Order's (CO) are reviewed for completeness, accuracy and compliance with applicable policies and procedures.Coordinate workflow and DePuy Synthes priorities of Document Control activities.Collaborate with Change Owners to efficiently analyze, manage and conduct COs.Conduct impact analyses of COs, assess change readiness and identify key requirements.Communicate CO status information as requested.Proactively seek methods of increasing efficiency while maintaining compliance in all areas of responsibility on a continuing basis.Provide historical and current documentation in response to queries from management and other departments as needed.Exhibit excellent organizational and communication skills.Properly employ all SOPs, Work Instructions, Training Guides and Forms in the performance of tasks within the organization.Maintain a work environment that provides open communication and personnel growth.Be an extremely flexible team player adaptable to change.Perform other special projects and support functions as assigned by the Supervisor.Required to know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times.Diligently participate in our compliance program-related activities as denoted by the Supervisor or our Chief Compliance Officer.
Caring for the world … one person at a time inspires and unites the people of Johnson & Johnson. This culture of caring is the focus of our corporate philosophy, that is anchored in the internationally applicable Credo. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.Main ResponsibilitiesAccountable for administration of the Change Order (CO) process.Accountable for compliance with the Food and Drug Administration's (FDA) Quality System Regulation (QSR) as it pertains to Documentation and Documentation Control.Accountable for the timely processing and release of new and changed controlled documents.Accountable that all Change Order's (CO) are reviewed for completeness, accuracy and compliance with applicable policies and procedures.Coordinate workflow and DePuy Synthes priorities of Document Control activities.Collaborate with Change Owners to efficiently analyze, manage and conduct COs.Conduct impact analyses of COs, assess change readiness and identify key requirements.Communicate CO status information as requested.Proactively seek methods of increasing efficiency while maintaining compliance in all areas of responsibility on a continuing basis.Provide historical and current documentation in response to queries from management and other departments as needed.Exhibit excellent organizational and communication skills.Properly employ all SOPs, Work Instructions, Training Guides and Forms in the performance of tasks within the organization.Maintain a work environment that provides open communication and personnel growth.Be an extremely flexible team player adaptable to change.Perform other special projects and support functions as assigned by the Supervisor.Required to know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times.Diligently participate in our compliance program-related activities as denoted by the Supervisor or our Chief Compliance Officer.
Pour un de nos Clients, actif dans le domaine de l'horlogerie , nous sommes à la recherche d'un régleur CNC (H/F) en horaire de nuit.Vous serez en charge de la mise en train complète , préparation et changement des outils,réglage et productionautocontrôle de la production sur décolleteuse ( fraisage en barre) Bumotec
Pour un de nos Clients, actif dans le domaine de l'horlogerie , nous sommes à la recherche d'un régleur CNC (H/F) en horaire de nuit.Vous serez en charge de la mise en train complète , préparation et changement des outils,réglage et productionautocontrôle de la production sur décolleteuse ( fraisage en barre) Bumotec
Caring for the world … one person at a time inspires and unites the people of Johnson & Johnson. This culture of caring is the focus of our corporate philosophy, that is anchored in the internationally applicable Credo. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.Medos International SARL, company part of the Johnson & Johnson Family of Companies, is recruiting a Quality System Engineer, located in Le Locle, Switzerland. This position will have responsibility for coordinating the Quality Systems activities at Legal manufacturer level and handling the performance and communication of the Quality metrics. Main ResponsibilitiesResolves quality issues by developing corrections, corrective actions and recommendations for any compliance issues for GSC base business activities.Participate for the timely execution of site NCs, CAPA and Audit Observations, by championing cross-collaboration across functions, sites, and operating companies; identifying barriers for the progress; and elevating issues for resolution and reporting of all Quality System metrics to management.Manage certificates, Declarations of Conformity of the site.Ensure timely and compliant execution of quality system requests and restrictions by driving cross-collaboration across functions.Ensures consistent and correct execution of change management procedures at the site to maintain the quality and compliance of the process and the records for document creation and changes.Creation and management of purchase orders.Identifies site needs to meet and improve system performance and raises to appropriate representative and management.Supports compliance activities by participating in audit readiness; assists in Internal and External audits.Participates in quality system improvement initiatives.
Caring for the world … one person at a time inspires and unites the people of Johnson & Johnson. This culture of caring is the focus of our corporate philosophy, that is anchored in the internationally applicable Credo. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.Medos International SARL, company part of the Johnson & Johnson Family of Companies, is recruiting a Quality System Engineer, located in Le Locle, Switzerland. This position will have responsibility for coordinating the Quality Systems activities at Legal manufacturer level and handling the performance and communication of the Quality metrics. Main ResponsibilitiesResolves quality issues by developing corrections, corrective actions and recommendations for any compliance issues for GSC base business activities.Participate for the timely execution of site NCs, CAPA and Audit Observations, by championing cross-collaboration across functions, sites, and operating companies; identifying barriers for the progress; and elevating issues for resolution and reporting of all Quality System metrics to management.Manage certificates, Declarations of Conformity of the site.Ensure timely and compliant execution of quality system requests and restrictions by driving cross-collaboration across functions.Ensures consistent and correct execution of change management procedures at the site to maintain the quality and compliance of the process and the records for document creation and changes.Creation and management of purchase orders.Identifies site needs to meet and improve system performance and raises to appropriate representative and management.Supports compliance activities by participating in audit readiness; assists in Internal and External audits.Participates in quality system improvement initiatives.
BESOINS PONCTUELS Mandaté par un de nos clients, Une manufacture spécialisée dans la joaillerie et afin renforcer leur département polissage ,Nous sommes à la recherche d'un polisseur Complet ( H/F) Polissage complet , préparation et Avivage - polisseur confirmé (or, argent en joaillerie)Mission longue durée, en horaire de journée:
BESOINS PONCTUELS Mandaté par un de nos clients, Une manufacture spécialisée dans la joaillerie et afin renforcer leur département polissage ,Nous sommes à la recherche d'un polisseur Complet ( H/F) Polissage complet , préparation et Avivage - polisseur confirmé (or, argent en joaillerie)Mission longue durée, en horaire de journée: