BD

Manufacturing Team member I - True Balloon Second Shift Job Description Summary Performs any combination of tasks involved in the manufacture and assembly of medical devices. Job Description Be Part of Something Bigger! BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics, and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues. Essential Job Functions: Responsible for following safety policies and procedures and all required GMP's and applicable manufacturing procedures. Perform a variety of duties to assemble all types and sizes of product, components and sub-assemblies using a variety of standard and specialty assembly machines or hand operations. May be required to press, bond, solder, flare, strip, clamp, sand, weld, mount/takedown or inspect for appearance, gauging of parts by "no-Go" or "go" gauges and set fixtures. After initial training, shows the ability to consistently meet daily production goals while building a high quality product, part or subassembly to specification. Set up, operates, perform minor maintenance and minor troubleshooting on equipment. Follow department procedures on material replenishment. Assists in training of manufacturing personnel. Participate in continuous improvement activities to enhance team performance. Must be able to work flexible hours and report to work on a regular, punctual basis. Ability to work with in a team environment and collaborate well with others. other related duties as assigned. BASIC QUALIFICATIONS Ability to read, write, interpret, comprehend and consistently follow written specifications in English. Able to perform basic math calculations and use measuring devices and tools. Meets or exceeds dexterity requirements. Ability to successfully demonstrate visual accuracy through company-approved program. Displays a positive attitude Able to work flexible and/or extended hours. Willingness to rotate into different tasks and responsibilities. Education and/or Experience: High school diploma or GED required Prior experience preferred, but not required. Physical Demands: Ability to work under magnification for long periods of time. Ability to stand or sit for long periods of time. Able to lift 30 lbs. (over 30 with assistance) Repetitive use of hands to finger, handle or fell, reach with hands and arms and/or perform repetitive hand/ wrist movement. Work Environment: May require some exposure to chemicals used in manufacturing processes. Some minor physical inconvenience or discomfort occasionally present in the work situation (moderate noise, disagreeable odors, etc.). May be subject to situations requiring precautions due to potential for minor injury or other health hazards. All applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin disability or veteran status. For certain roles at BD, employment is contingent upon the Company s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our associates can fulfill their life s purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth, and life balance components - is designed to support the varying needs of our diverse and global associates. To learn more about BD visit Becton, Dickinson, and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate based on race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. Primary Work Location USA NY - Glens Falls Additional Locations Work Shift US BD 2nd Shift 1pm-930pm (United States of America) Show More Show Less Apply Save Job

Operations Leader (Night Shift) Job Description Summary Responsible for leading the activities of a high-volume manufacturing operation and building a high performing team of production associates. Achieves department s Safety, Quality, Delivery, Cost, & People goals through leadership and teamwork. Job Description Be part of something bigger! BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues. Work Hours Monday - Friday Night Shift 3:00 PM - 12:00 AM (midnight) RESPONSIBILITIES Takes ownership for the performance and results of the shift and department. Creates organizational clarity and empowers the team to make good decisions. Communicates department goals, objectives, and initiatives to the production floor in a simple and concise manner. Ensures a safe working environment, implements safety policies. Processes accident reports. Ensures manufactured products meet the established quality requirements. Works with the Quality team to implement new or revised quality plans. Exhibits a Continuous Improvement (CI) approach. Aims to consistently improve self and team. Cultivates a learning environment where mistakes and failures are used as opportunities to grow. Develops team personnel. This includes hiring, promoting, rewarding, terminating associates, and setting/managing overtime for the department. Builds technical competence by ensuring team members are trained to perform their jobs and can progress in the future. Manages training within the department to ensure team members understand and follow Standard Work and Good Manufacturing Practices. Updates and monitors team member learning plans in C2C. Performs regular, timely, and accurate assessments of team members. Provide mentorship and candid feedback to the team. Ensures fair and reasonable application of company and departmental policies and practices, such as vacation, sick, attendance and FMLA. Follow: all local, state, federal, and BD safety regulations, policies, and procedures includes RCRA Hazardous Waste regulations; and all local BD quality policies, procedures, and practices through consistent application of sound quality assurance principles. Other duties as assigned. SUPERVISION: Supervise team of 20+ team members consisting of: production associates responsible for running the line maintenance associates responsible for mechanical maintenance quality associates responsible for in-process sampling area leaders responsible for general line support EDUCATION AND EXPERIENCE High School diploma or GED equivalent required Preferred: Bachelor s degree and experience in a highly automated manufacturing environment. For certain roles at BD, employment is contingent upon the Company s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why join us? A career at BD means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our associates can fulfill their life s purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth, and life balance components - is designed to support the varying needs of our diverse and global associates. To learn more about BD visit Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. Primary Work Location USA UT - Sandy Additional Locations USA UT - Salt Lake City, USA UT - Salt Lake City BAS, USA UT - Salt Lake City BPV Satellite Work Shift Show More Show Less Apply Save Job

Manufacturing Team Member I - Nitinol 1st Shift (onsite) Job Description Summary Performs any combination of tasks involved in the manufacture and assembly of medical devices. Job Description Be part of something bigger! BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues. Up to $2,500 hiring incentive being offered to new hires based on manufacturing position eligibility. 2nd Shift: M-F 1PM - 9PM Position Summary: Performs any combination of tasks involved in the manufacture and assembly of medical devices. Essential Job Functions: Responsible for following safety policies and procedures. Responsible for following all required GMP s and applicable manufacturing procedures. Perform a variety of duties to assemble all types and sizes of product, components, and sub-assemblies using a variety of standard and specialty assembly machines or hand operations. May be required to press, bond, solder, flare, strip, clamp, sand, weld, mount/takedown or inspect for appearance, gauging of parts by "no-go" or "go" gauges and set fixtures. After initial training, shows the ability to consistently meet daily production goals while building a high quality product, part or subassembly to specification. Set up, operates, perform minor maintenance and minor troubleshooting on equipment. Follow department procedures on material replenishment. Assists in training of manufacturing personnel. Participate in continuous improvement activities to enhance team performance. Must be able to work flexible hours and report to work on a regular, punctual basis. Ability to work in a team environment and collaborate well with others. Other duties as assigned. Basic Qualifications: Ability to read, write, interpret, comprehend and consistently follow specifications written in English. Able to perform basic math calculations and use measuring devices and tools. Meets or exceeds dexterity requirements. Ability to successfully demonstrate visual accuracy through company-approved program. Displays a positive attitude. Able to work flexible and/or extended hours. Willingness to rotate into different tasks and responsibilities. Education and/or Experience: High School Diploma, GED, or Minimum of one (1) year medical device manufacturing experience, plus Minimum one (1) year of consecutive work experience. Physical Demands: Ability to work under magnification for long periods of time. Ability to stand or sit for long periods of time. Able to lift 30 lbs. (over 30 lbs. with assistance). Repetitive use of hands to finger, handle, or feel, reach with hands and arms and/or perform repetitive hand/wrist movement. Work Environment: May require some exposure to chemicals used in manufacturing processes. Some minor physical inconvenience or discomfort occasionally present in the work situation (moderate noise, disagreeable odors, etc.). Appropriate Personal Protective Equipment (PPE) will be provided. Training Requirements: On-the-Job, Standard Operating Procedures (SOP s) required for position, and Good Manufacturing Practices (GMP). For certain roles at BD, employment is contingent upon the Company s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why join us? A career at BD means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our associates can fulfill their life s purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth, and life balance components - is designed to support the varying needs of our diverse and global associates. To learn more about BD visit Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. Primary Work Location USA NY - Glens Falls Additional Locations Work Shift US BD 2nd Shift 1pm-930pm (United States of America) Show More Show Less Apply Save Job

Cybersecurity Officer, Dispensing Job Description Summary Job Description Be part of something bigger! BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues. Cybersecurity Officer, Dispensing The Cybersecurity Officer, Dispensing is responsible for managing the information security program of one of BD s largest medical device business units. This person will ensure BD products, solutions, and services are secure by design, in use, and through partnership with customers and other third-party entities. They will oversee the performance of risk assessments, management and communication of vulnerabilities and threats, delivery of awareness and training, quality of release deliverables, and engagement with leadership teams. The Cybersecurity Officer will engage R&D, Operations, Quality, Contract, Marketing, Sales, and fellow Information Security colleagues to ensure security is integrated across all functions. Responsibilities: Oversee the execution of information security deliverables and processes Develop and manage security goals for their organization Report on the status of annual objectives, vulnerabilities, and remediation planning Provide guidance to teams on the incorporation of security within development and operations Manage team members in the performance of their duties Ensure alignment with the broader BD Information Security organization Drive process improvement of security practices Other duties as required Scope: The scope of security oversight for this role includes application development, DevOps, and devices deployed at customer sites. They will oversee the performance of risk assessments, management of vulnerabilities and threats, delivery of awareness and training, quality of release deliverables, and delivery of status reports to management. They will engage stakeholders within their organization and fellow Information Security colleagues to ensure alignment to Quality Management System procedures and industry best practices. Minimum Qualifications: Minimum of 8 years of information security experience Minimum of 8 years in a medical device development organization Minimum of 2 years of project or program management experience Degree level qualification; or equivalent combination of education and experience. Knowledge, Skills & Abilities: Ability to develop, achieve consensus, and drive achievement of goals Understanding of product development processes and secure development lifecycle Understanding of information security and privacy principles Able to be strategic, but also drive tactical execution; willing to roll up sleeves and get the job done. Able to interface with multiple levels and disciplines within the organization. Able to translate cybersecurity requirements (technical and regulatory) in a way that is understood by technical and non-technical associates alike. Knowledge of medical device industry regulations; FDA pre/post market guidance for medical devices, NIST 800-53, FIPS 140-2, AAMI TIR57 preferred Experience and background in software development preferred For certain roles at BD, employment is contingent upon the Company s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why join us? A career at BD means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our associates can fulfill their life s purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth, and life balance components - is designed to support the varying needs of our diverse and global associates. To learn more about BD visit Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. PDN Primary Work Location USA CA - San Diego TC Bldg C&D Additional Locations Work Shift Show More Show Less Apply Save Job

Gestionnaire R&D Job Description Summary Le Gestionnaire R&D est responsable de la planification, la coordination et la gestion des activités d'une ou plusieurs sections de projets ou d un projet complet, pour le département de la R&D. Il assure la supervision de la planification de son projet à long terme et à court terme, ce qui nécessite généralement une interaction avec le management de Projets, la Fabrication, la Qualité et les Affaires Réglementaires. Il surveille et évalue l'exécution des tâches reliées aux projets. La portée du projet peut comprendre le développement de nouveaux produits et technologies et/ou l amélioration de produits existants. Le Gestionnaire R&D est garant de la définition, du développement, de la qualification et du transfert au département de la production, de réactifs et méthodes associées pour le diagnostic in vitro. Il est en mesure de concevoir et d élaborer de nouveau concept de produits de diagnostic in vitro et contribue à bien définir et établir des normes d'excellence en technologie et politiques de développement. Il peut également agir à titre de membre du Core Team sur les équipes GPDS ou peut le faire également par le biais d'un représentant. Job Description Sommaire Le Gestionnaire R&D est responsable de la planification, la coordination et la gestion des activités d'une ou plusieurs sections de projets ou d un projet complet, pour le département de la R&D. Il assure la supervision de la planification de son projet à long terme et à court terme, ce qui nécessite généralement une interaction avec le management de Projets, la Fabrication, la Qualité et les Affaires Réglementaires. Il surveille et évalue l'exécution des tâches reliées aux projets. La portée du projet peut comprendre le développement de nouveaux produits et technologies et/ou l amélioration de produits existants. Le Gestionnaire R&D est garant de la définition, du développement, de la qualification et du transfert au département de la production, de réactifs et méthodes associées pour le diagnostic in vitro. Il est en mesure de concevoir et d élaborer de nouveau concept de produits de diagnostic in vitro et contribue à bien définir et établir des normes d'excellence en technologie et politiques de développement. Il peut également agir à titre de membre du Core Team sur les équipes GPDS ou peut le faire également par le biais d'un représentant. Tâches Est en charge d un projet et agit en tant que coach auprès des membres de son équipe pour s assurer du respect des échéanciers et de la résolution des problèmes techniques ou opérationnels. Gère la charge de travail, assigne les tâches et évalue le rendement des membres de son équipe. Avec l employé, détermine les objectifs personnels de performances et assure les suivis appropriés. Il est responsable de l évaluation annuelle de chaque employé sous sa responsabilité. En respect avec les différents échéanciers de son projet, il établit les plans de travail des différentes phases de développements. En respectant les règles relatives à l assurance qualité, assure la rédaction de toute la documentation requise pour son projet (protocoles, rapports, etc.). Comprends et est en mesure d évaluer les différentes approches scientifiques disponible pour le développement de produits de diagnostic moléculaire. Évalue avec un sens critique les données, les résultats et l évolution d un projet et apporte des recommandations sur la qualité de l exactitude et précision des tests. Contribue à l identification de nouveaux concepts innovants et au dépôt de nouveaux brevets. Organise des séances d informations et des réunions techniques pour pour le personnel de direction de la fonction et auprès de son équipe. Dans le cadre de son projet, peut être en contact avec des gestionnaires de même niveau provenant de différentes fonctions (Affaires Réglementaires, Affaires Médicales, Opérations, Qualités, Marketing, Système, etc.) à propos de décisions opérationnelles, ou des exigences de planification. Contribue à l excellence fonctionnelle. Passe en revue l avancement de son projet avec son supérieur immédiat. Formation académique Doctorat dans une discipline scientifique (biologie moléculaire, microbiologie ou virologie) ou l équivalent (maîtrise dans une discipline scientifique en plus de 8 années d expériences pertinentes). Expérience requise Minimum de 3 ans d expérience dans un environnement de recherche spécialisée en développement de produits de diagnostic in vitro et dans un milieu de travail réglementé combiné à une expérience pertinente dans la gestion d une équipe. Compétences Savoir Bilingue (Français-Anglais) Expérience dans un environnement ISO13485 et " Quality System Regulation ". Connaissance techniques et scientifiques (e.g. PCR, microbiologie, etc.). Savoir faire De bonnes capacités en communication et en leadership ainsi que de solides compétences interpersonnelles sont essentielles pour assurer le succès dans le poste. Niveau de prise de décision opérationnel et stratégique. Savoir être Orienté vers l action et les résultats. Sens de l organisation, jugement, souci du détail et fiabilité. Gestion de l ambiguïté : polyvalence, flexibilité et capacité d adaptation. Gestion de personnel Dirige une équipe de superviseur et de scientifiques composés de 5 à 10 employés. Conditions spécifiques Nécessite une grande disponibilité et flexibilité en fonction des besoins qui sont très variables. Peut nécessiter d être disponible pour des déplacements (moins de 10% du temps). Primary Work Location CAN Québec - GeneOhm Sciences Additional Locations Work Shift Show More Show Less Apply Save Job