Amick Brown is seeking an experiencedDesign Control Engineer for our direct client. Location:Sunnyvale, CA Duration: 5 Months.Description
Joining our clients means joining a team dedicated to using technology to benefit patients by improving surgical efficacy and decreasing surgical invasiveness, with patient safety as our highest priority.
Primary Function of Position
The mission of Supplier Engineering is to ensure high quality and stable delivery of purchased production components from suppliers operating under robust quality systems to maximize Patient Value.
This role will support managing and tracking of NCRs caused by suppliers, by using data analytics, and performance metrics to improve timely closures of NCRs.
Roles and Responsibilities
Supplier Quality and Performance Improvement
Drive NCR reduction and manage NCRs completion related to supplier caused issues, ensuring NCRs get assigned, approved, and closed in timely manner
Use data analytics to create NCR and performance metrics reports. E.g Pareto Charts
Drive meetings and follow up on closures of NCRs.
Investigate and resolve ISI Production line down events that are Supplier related; includes the following:
Disposition non-conforming material (Containment)
Root Cause Analysis
Implement Corrective Actions/Preventive Actions
Documenting all of the above
In order to adequately perform the responsibilities of this position the individual must possess:
BS degree in Engineering or equivalent
2-7 years related experience in Manufacturing Engineering, Supplier Quality Engineering, or related field
Excellent written and verbal communication skills
Data Analytics, Metrics reporting,
Dependable Project Management skills
In-depth analytical and trouble-shooting skills
Experience with driving NCR improvements
Ability to read and interpret detailed specification drawings and communicate technical information
Advanced computer experience using Windows, MS Office Suite, SAP (or other ERP system), and Agile (or other document control system)
Knowledge of 21 CFR part 820 and ISO 13485 (experience in auditing suppliers to these standards)
Experience in a high-volume medical device company
We are an AA/EEO/Veterans/Disabled employer
Amick Brown is an Information Technology consulting company specializing in ERP, Data Analytics, Information Security, Application Development, Networking, and Cloud Computing. The company was founded in 2010 and is headquartered in San Ramon, California.Regular full-time employees are eligible for the following Amick Brown provided benefits:
VIEW JOBS11/24/2022 12:00:00 AM2023-02-22T00:00<p>Company Description</p><p>At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.</p><p>As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare's hardest challenges and advance what is possible.</p><p>Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere. We strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves.</p><p>Passionate people who want to make a difference drive our culture. Our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential.</p><p>Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let's advance the world of minimally invasive care.</p><p>Job Description</p><p>The Mechanical Design Engineer must utilize creativity and sound engineering judgment in the design of parts and subassemblies of next generation mechanical systems for medical capital equipment. The Mechanical Design Engineer is expected to use machine design and analytical skills to conceptualize, develop, and verify new mechanical designs. They are responsible for key system components and will interface with suppliers and manufacturing to build high-quality hardware prototypes and productize new designs. The Mechanical Engineer should be capable of making sound decisions when faced with the time constraints and ambiguous or incomplete information typical of research and development. Apply today and join one of the most exciting mechanical design and mechanical systems teams working on world-class surgical robotics.</p><p>Roles & Responsibilities</p><ul><li><p>Designing components and producing mechanical drawings in a regulated environment for volume manufacturing processes which may include cast metal, injection molded plastic, sheet metal stamped, and others</p></li><li><p>Working within multi-disciplinary teams to define requirements for new and current designs</p></li><li><p>Rapid development and iteration of full-scale prototypes of candidate architectures to satisfy requirements</p></li><li><p>Developing mechanical assemblies, with careful consideration for key functions and safety</p></li><li><p>Designing for manufacturability, reliability, serviceability, and cost</p></li><li><p>Selecting and managing vendors in the prototype phase</p></li><li><p>Collaborating with manufacturing to create product assembly tooling, fixtures, and instructions</p></li><li><p>Developing and performing component verification testing and product validation testing</p></li><li><p>Supporting production of final product by troubleshooting process and component problems</p></li><li><p>Providing engineering support to Manufacturing, Test Engineering, and Service to facilitate transfer of designs</p></li></ul><p>Qualifications</p><p>Skills, Experience, Education, & Training</p><p>Required</p><ul><li><p>Minimum BSME, or similar</p></li><li><p>Interest in the medical applications of robotics</p></li><li><p>Ownership of key components or assemblies through multiple products</p></li><li><p>Comfortable with all phases of the product development lifecycle including design, implementation, debug, verification, qualification, and transfer</p></li><li><p>Passion for details in creating robust and reliable machines designed for mission-critical applications</p></li><li><p>Experience designing for volume manufacturing processes such as metal casting, plastic injection molding, sheet metal stamping, compression molding, thermoforming, etc.</p></li><li><p>Ability to apply knowledge of engineering materials and component selection criteria to product designs through strong concept development, design analysis, hands-on prototyping, and reliability testing skills</p></li><li><p>Proficiency using CAD, analysis</p></li><li><p>Excellent communication and interpersonal skills</p></li><li><p>Self-driven with the ability to excel in a high-energy, small, focused team environment, to maintain a strong sense of shared responsibility and reward, and to make work fun and interesting</p></li><li><p>Preferred</p></li><li><p>Post-graduate study or equivalent work experience preferred</p></li><li><p>Robotics or Mechanical Systems design experience. Surgical or medical device product experience is a plus.</p></li><li><p>Ability to execute and document component and assembly changes in an automated change control system and demonstrate that the changes were made properly</p></li><li><p>Effective collaboration with multi-disciplinary functions like clinical, human factors, industrial design, interaction design, etc.</p></li><li><p>Experience with Finite Element Simulation (FEM, FEA ,CFD, Multiphysics, etc.) tools to design mechanical assemblies</p></li><li><p>SolidWorks experience</p></li></ul><p>Additional Information</p><p>Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19. Details can vary by role.</p><p>Intuitive is an Equal Employment Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws.</p><p>We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.</p><p>Shift : Day</p><p>Travel : 10% of the time</p><br>Intuitive SurgicalSunnyvaleCA
VIEW JOBS11/23/2022 12:00:00 AM2023-02-21T00:00<p>Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 113,000 colleagues serve people in more than 160 countries.</p><p>About Abbott</p><p>Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology.</p><p>Working at Abbott</p><p>At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:</p><ul><li><p>Career development with an international company where you can grow the career you dream of.</p></li><li><p>Free medical coverage for employees* via the Health Investment Plan (HIP) PPO</p></li><li><p>An excellent retirement savings plan with high employer contribution</p></li><li><p>Tuition reimbursement, the Freedom 2 Savestudent debt program and FreeUeducation benefit - an affordable and convenient path to getting a bachelor's degree.</p></li><li><p>A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.</p></li><li><p>A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.</p></li></ul><p>Our location in Temecula, CA currently has an opportunity for a Quality Engineer.</p><p>The Opportunity</p><p>This position works out of our Temecula, CA location in the Abbott Vascular Division. Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine ﬁngersticks. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease.</p><p>What You'll Work On</p><p>A Design Assurance Engineer assures new or modified products conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs</p><p>MAIN RESPONSIBILITIES</p><ul><li><p>Execute and support on-time completion of Design Control Deliverables.</p></li><li><p>Support on-time execution of Quality Plans for internal development, OEM-based, Clinical Product Development (CPDP), and design change projects.</p></li><li><p>Accountable for Design Verification and Validation planning & execution, including active cross-functional root-cause analysis investigation & resolution activities.</p></li><li><p>Lead or support Risk Management activities from product Concept through Commercialization.</p></li><li><p>Support design test and inspection method development, and lead method validation activities.</p></li><li><p>Ensure DHF content completion, integrity, and regulatory & standards compliance; collaboratively communicating & resolving gaps.</p></li><li><p>Support manufacturing process development & qualification for new product commercialization and product changes.</p></li><li><p>Support internal & external audit responses.</p></li><li><p>Support product re-certifications.</p></li><li><p>Support the establishment of objective, measurable, discrete, and verifiable customer and product requirements.</p></li><li><p>Complete Document Change Request Reviews in a timely and objective manner.</p></li><li><p>Additional duties may be identified by functional management based on the current project/business objectives.</p></li><li><p>Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.</p></li><li><p>Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.</p></li></ul><p>Minimum Experience / Training Required</p><p>Bachelors Degree Engineering or Technical Field and/or an equivalent combination of education and work experience. Masters Degree Preferred</p><ul><li><p>Minimum 2 years previous Quality engineering experience and demonstrated use of Quality tools/methodologies</p></li><li><p>Experience working in a broader enterprise/cross-division business unit model preferred.</p></li><li><p>Ability to work in a highly matrixed and geographically diverse business environment.</p></li><li><p>Ability to work within a team and as an individual contributor in a fast-paced, changing environment.</p></li><li><p>Ability to leverage and/or engage others to accomplish projects.</p></li><li><p>Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.</p></li><li><p>Multitasks, prioritizes and meets deadlines in timely manner.</p></li><li><p>Strong organizational and follow-up skills, as well as attention to detail.</p></li><li><p>Ability to travel approximately 10%, including internationally.</p></li></ul><p>Apply Now</p><ul><li>Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.</li></ul><p>Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com</p><p>Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life.</p><p>Abbott is an Equal Opportunity Employer, committed to employee diversity.</p><p>Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbottand on Twitter @AbbottNews and @AbbottGlobal.</p><br>Abbott LaboratoriesSunnyvaleCA
VIEW JOBS11/23/2022 12:00:00 AM2023-02-21T00:00<p>OBJECTIF PRINCIPAL DU POSTE</p><ul><li><p>Développer La part de marché Abbott NMD sur la gamme de traitement par Radio fréquence sur le marché du traitement de la douleur Chronique</p></li><li><p>Maintenir la dynamique des centres clients</p></li><li><p>Conquérir de nouveaux clients grâce au focus sur ce segment</p></li><li><p>Structurer l'offre capital equipement, accessoires, contrat de service</p></li><li><p>Prendre part à l'offre parcours patient dans le traitement de la douleur chronique</p></li><li><p>Contribuer au positionnement d'Abbott NMD en tant que leader dans le traitement de la douleur</p></li></ul><p>MISSIONS ET RESPONSABILITES PRINCIPALES</p><p>Sous la responsabilité du country manager</p><ul><li><p>Développer la connaissance et la pénétration de la gamme RF</p></li><li><p>Développer les clients existants en volume et en chiffre d'affaires</p></li><li><p>Prospecter et ouvrir de nouveaux comptes clients, développer de nouvelles indications</p></li><li><p>Atteindre les objectifs de vente fixés pour les gammes de produits dont il a la charge, dans le cadre du plan défini</p></li><li><p>Travailler en collaboration avec les équipes France et EMEA Cliniques et Marketing afin d'implanter la marque IONIC RF</p></li><li><p>Etablir un plan de développement à 2 ans</p></li><li><p>Contribuer au projet de l'équipe NMD France et à la reconnaissance de la division auprès des anesthésistes, Neurochirurgiens, chirurgiens orthopédistes, radiologues interventionnels et des établissements exerçant nos spécialités.</p></li><li><p>Identifier les intervenants dans le processus d'achat au sein de chaque établissement</p></li><li><p>Négocier en connaissance des financements liés à l'activité</p></li><li><p>Contribuer au plan de communication national auprès des autorités de santé et des associations de patients</p></li><li><p>Suivre les stratégies et programmes spécifiques mis en place au niveau national et régional afin d'augmenter les parts de marché</p></li><li><p>Approfondir son développement des connaissances sur les nouvelles gammes de produits et thérapies de la Société et assurer la veille concurrentielle</p></li><li><p>Suivre toutes les formations demandées par le groupe et le manager afin d'obtenir, le cas échéant, les certifications ou rectifications requises</p></li><li><p>Maintenir une bonne compréhension de l'environnement et des enjeux économiques de son domaine d'activité</p></li><li><p>Assurer la formation et l'accompagnement des équipes médicales</p></li><li><p>Respecter la politique commerciale de la Société au niveau des prix, des offres commerciales, des conditions de paiement en accord avec les procédures appels d'offres et de l'engagement des dépenses</p></li><li><p>Anticiper et identifier les besoins des clients afin de préparer la réponse la plus adaptée et innovante pour les appels d'offres en coordination avec tous les services concernés</p></li><li><p>Faire un Reporting régulier à sa hiérarchie au-delà des Business Review trimestrielle</p></li><li><p>Contrôler et mettre en place des actions de suivi et de retrait, le cas échéant, pour les produits en date limite d'utilisation (UBD) en coordination avec son supérieur hiérarchique, le Field Inventory Specialist, le Customer Service, la Qualité, la Supply Chain…</p></li><li><p>Réaliser le contrôle des stocks en dépôt conformément aux directives et assurer la traçabilité de tous les dispositifs en dépôt sur votre secteur ou en votre possession, en conformité avec les procédures qualité</p></li></ul>Abbott LaboratoriesSunnyvaleCA
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