[{"country_short": "USA", "city": "Sunnyvale", "description": "Engineer, Senior Software\nJob Requisition #: 12499\nDate Posted: 04/13/2012\nCategory: Software\nLocation: Sunnyvale - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open in Sylmar, CA.\n\nJob Overview\nWorking without appreciable supervision, performs moderate risk/highly complex software project activities in such areas as Development Engineering, IT Engineering, System Engineering, Test Engineering, and/or related areas. Assignments may include, but are not limited to, the designing, developing, updating, and maintaining of different software specifications as well as the troubleshooting, debugging, and maintaining of software, test, or tool designs, cases, scripts, procedures, and/or code at a multiple sub-systems or application levels. Assignments may also include capturing, gathering, analyzing, maintaining, and validating applicable product or software requirements. Work requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more academic course of study. Applies advanced engineering and scientific principles to the evaluation and solution of technical problems. Initiates the planning, organizing, performing, coordinating and/or directing of engineering work. Performs technical studies. Remains abreast of and consults on technical advancements. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness.\n\nRequirements/Education: Bachelors Degree in Computer Science, a related field, or equivalent. Typically a minimum of six plus years of progressively more responsible work experience in a range of software engineering disciplines using a variety of programming methods. Broad cross-disciplinary and in-depth knowledge of the software engineering profession. A comprehensive familiarity with commodity/off-the-shelf software tools, and programs. A qualified record of implementing new processes to existing software and related systems. Requires comprehensive written and verbal communication, interpersonal, facilitation, presentation, quantitative, analytical, organizational, follow-up skills, and the ability to meet deadlines on multiple projects as well as the ability to converse effectively with all levels of employees. A documented record of delivering software engineering information which adds value to managements decision making process is required. A demonstrated ability to understand and comply with applicable FDA regulations and Company operating procedures, processes, policies, and tasks is also required. Advanced personal computer skills including spreadsheet, word processing database management, and specialized applications. Must be able to handle multiple assignments. Must be able to perform in a diverse cross-functional team environment.\n\nDesired Requirements: An advanced credential in a relevant discipline/concentration. Specialized experience and/or relevant coursework related to the software applications, programs, and processes. Academic or in-house courses in project management, leadership, training, TQM, and various technical applications as noted above.\n\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-05-11 18:45:08", "url": "http://jobs.sjm.com/xml/28634552/job", "country": "United States", "company": "St. Jude Medical", "title": "Engineer, Senior Software", "reqid": "12499", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 28634552}, {"country_short": "USA", "city": "Sunnyvale", "description": "Sr. Software Development Engineer\nJob Requisition #: AF13663\nDate Posted: 04/27/2012\nCategory: Software Engineering\nLocation: Sunnyvale - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Atrial Fibrillation Division.\n\nJob Overview\nWe are seeking an experienced, high caliber Senior Software Engineer to meet our standard product development needs as well as increase our ability to deliver integrated hardware and software solutions to meet our project specific requirements.\n\nImpact this role will have within the AF division:\n\u2022 The Senior R&D Software Engineer designs and develops application software for RF ablation systems.\n\u2022 This role writes product requirement documents, designs, develops code, unit tests and helps out the verification team.\n\nRequired Qualifications:\n\u2022 Bachelor\u2019s degree in Computer Science, Computer or Electrical Engineering\n\u2022 7 + years hands-on development experience with real-time embedded hardware, software design and development, and programming experience in C/C++, QT, Object Oriented programming with knowledge of Hardware interfaces and microprocessors\n\u2022 Experience with Linux, or other real time operation system, OS kernel module, device driver development\n\u2022 Familiarity with software configuration and software defect tracking systems\n\u2022 Demonstrated ability to understand and comply with applicable FDA regulations and Company operating procedures, processes, policies, and tasks\n\u2022 Effective verbal and written communication skills to interact with associates at all levels of the organization, vendors and other SJM entities\n\u2022 Adaptability to frequent change in the work environment\n\u2022 Ability to prioritize responsibilities and ensure deadlines are met\n\u2022 Proficient working knowledge of MS Word, Outlook, PowerPoint, Excel and Project\n\u2022 Experience with 3D image processing, registration and rendering software design, Wireless protocols\n\u2022 Polished communicator- written documentation and oral presentations/ discussions/ meetings\n\u2022 Excellent reputation for building relationships across various levels of an organization.\n\u2022 Organized, on-time, and detailed project management skills.\n\u2022 Energized attitude.\n\nPreferred Qualifications:\n\u2022 Masters degree in Computer Science, Computer or Electrical Engineering\n\u2022 Experience with RTOS, debugging tools and good software development processes\n\u2022 Working knowledge of entire software development and test cycle with at least one complete FDA regulated medical device product development cycle. Knowledge of applicable international regulations and standards (QSR, ISO 13485, ISO14971)\n\u2022 Formal training in Program/Project Management or Program Management Professional Certification\n\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-04-27 19:56:25", "url": "http://jobs.sjm.com/xml/28240250/job", "country": "United States", "company": "St. Jude Medical", "title": "Sr. Software Development Engineer", "reqid": "AF13663", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 28240250}, {"country_short": "USA", "city": "Sunnyvale", "description": "RF Characterization Engineer\nJob Requisition #: 12377\nDate Posted: 04/13/2012\nCategory: Electrical Engineering\nLocation: Sunnyvale - CA - USA\nSylmar - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management Division (CRMD):\n\nJob Overview\nWe are seeking a hands-on technical RF Characterization Engineer to work on RF characterization from IC to system level on implantable biomedical products.  These implantable pacemakers and implantable defibrillators save lives and provide therapy for serious medical conditions.\n\nOur devices are complex, low-power, embedded systems and include custom analog, digital, and mixed signal ICs, hybrids, and discrete components. The successful person in this role will have a good RF background with hands-on RF characterization experience and good breadth of electrical engineering knowledge.\n\nThe RF Characterization Engineer will comprehensively analyze designs, create appropriate characterization test plans with rationale for choices, critically evaluate results, and trouble-shoot through challenging problems.  This person will also work closely with other cross-functional groups such as Design, ATE, Firmware, Clinical Systems, and Manufacturing.\n\nRequired Skills:\n\n\u2022 MSEE with at least 2 years RF systems experience or BSEE with at least 3 years RF systems experience\n\u2022 Theoretical and practical understanding of RF at system level\n\u2022 Hands on RF characterization including use of RF bench equipment\n\u2022 Strong technical analysis and troubleshooting skills for products containing RF, analog / digital ICs, discrete components, embedded systems\n\u2022 Excellent interpersonal and communication skills with ability to multi-task\n\u2022 Track record working collaboratively across functions in successful product development\n\u2022 Demonstrated ability to organize, analyze, document, prepare for characterization test plans, reviews, and reports\n\u2022 Ability to pick things up quickly\n\u2022 Motivated to learn about and ability to lead biomedical product development\n\nDesired Skills:\n\n\u2022 RF IC and RF Systems experience including ATE and bench equipment\n\u2022 Programming skills in C, LabWindows CVI\n\n\n\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-04-13 20:07:09", "url": "http://jobs.sjm.com/xml/27882978/job", "country": "United States", "company": "St. Jude Medical", "title": "RF Characterization Engineer", "reqid": "12377", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 27882978}, {"country_short": "USA", "city": "Sunnyvale", "description": "Mixed Signal IC Design Engineer\nJob Requisition #: 12378\nDate Posted: 04/13/2012\nCategory: Electrical Engineering\nLocation: Sunnyvale - CA - USA\nSylmar - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management Division (CRMD):\n\nJob Overview\nMixed Signal IC Design Engineer\n\nWe are seeking a talented and versatile IC designer to be a part of our Integrated Circuit Development organization. Our team designs ultra-low power mixed-signal IC\u2019s for use in St. Jude Medical\u2019s implantable pacemakers and defibrillators. These devices save lives and provide therapy for serious medical conditions.\n\nThe successful person in this role will have a solid mastery of mixed-signal IC design, with breadth and depth of knowledge across digital and analog design. In this role, the engineer will work closely with other members of the Analog and Digital Design groups, and play a key role in growing our mixed-signal design, and system-on-a-chip development capability.\n\nRequired Skills:\n\n- Solid background in analog IC design, knowledge of MOS device physics and design experience with common building blocks such as op amps, bias generators, bandgap references, switched capacitor circuits, etc.\n- Strong knowledge of simulation test bench development for mixed-signal (analog and digital) simulations, excellent simulation and debug skills, and working knowledge of mixed-signal testing.\n- Experience with Modelsim, NC-Verilog, VCS or similar digital logic simulators.\n- Experience with Verilog, C, and/or System Verilog.\n- Knowledge of the basic elements of writing synthesizable Verilog RTL code, including simple state machines, hardware register interfaces to an embedded MCU, and hierarchical design\n- Working knowledge of Matlab is desired.\n- Excellent verbal and written communications skills, and ability to work collaboratively in a team environment.\n- Demonstrated ability to clearly document design work and present and explain design choices.\n- Ability to work as part of a cross-functional and cross-site team, and design circuits with consideration for overall System Requirements\n\nEducation and Experience Requirements:\nBSEE or equivalent degree required, MSEE or equivalent preferred\nAt least 6 years industry experience in IC design\n\n\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-04-13 20:07:09", "url": "http://jobs.sjm.com/xml/27882979/job", "country": "United States", "company": "St. Jude Medical", "title": "Mixed Signal IC Design Engineer", "reqid": "12378", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 27882979}, {"country_short": "USA", "city": "Sunnyvale", "description": "Senior RF Software/Hardware Engineer\nJob Requisition #: 12376\nDate Posted: 04/13/2012\nCategory: Software\nLocation: Sunnyvale - CA - USA\nSylmar - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management Division (CRMD):\n\nJob Overview\nWe are seeking a talented and versatile RF Engineer with strong software skills to be a part of our RF Telemetry Hardware organization. Our team is responsible for the RF hardware design for use in St. Jude Medical\u2019s implantable pacemakers and defibrillators. These devices save lives and provide therapy for serious medical conditions. The RF telemetry system provides a critical communication link between those implantable devices and external programmers and interrogators.\n\nThe successful person in this role will have a strong background in firmware or software design, and a solid understanding of RF engineering. In this role, the engineer will work closely with other members of the RF and electrical system design groups, and play a key role in growing our RF telemetry capability.\n\nResponsibilities:\n\n- Software and Firmware design for RF hardware system design and characterization for implantable and external medical devices\n- Create software for RF system prototypes for output power measurements, optimization, tuning, sensitivity and parametric measurements.\n- RF laboratory measurements, including:\no Measurement of small antenna performance in TEM cells\no Evaluation of small inductive/magnetic loop antennas.\n- Develop, maintain, and support characterization firmware for use in RF system development\n- Interface with customers, vendors, and other department functions (manufacturing, mechanical designers, etc).\n\n\nRequired Skills:\n\n- BSEE (MSEE preferred) and at least 5+ years of experience in software and/or firmware design, with a strong background in RF\n- Programming experience in C, C++, and LabWindows CVI\n- Firmware programming experience on embedded microcontrollers\n- Proven ability to develop structured, revision-controlled code used by various other groups/organizations\n- Excellent RF laboratory skills, including the use of spectrum analyzers, network analyzers, power meters, slide-screw tuners, test automation, etc.\n- Familiar with BER, polarization, free space loss, S-parameters, Smith Charts, and other RF measurements and performance metrics\n- Ability to grow and adapt to other work functions.\n- Capable of independent work as well as part of small teams.\n- Excellent verbal and written communications skills, and ability to work collaboratively in a team environment.\n- Demonstrated ability to clearly document design work and present and explain design choices.\n- Ability to work as part of a cross-functional and cross-site team, and design circuits with consideration for overall System Requirements\n\n\n\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-04-13 20:07:08", "url": "http://jobs.sjm.com/xml/27882976/job", "country": "United States", "company": "St. Jude Medical", "title": "Senior RF Software/Hardware Engineer", "reqid": "12376", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 27882976}, {"country_short": "USA", "city": "Sunnyvale", "description": "Technical Service Engineering Specialist\nJob Requisition #: 12699\nDate Posted: 04/11/2012\nCategory: Technical Services\nLocation: Sunnyvale - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management business unit, located in Sunnyvale, CA:\n\nJob Overview\nFunctioning under general supervision in accordance with established policies/procedures, provides independent clinical and technical support in response to inquiries from physicians, health care professionals, patients and field staff using professional knowledge and judgment. This level of the Technical Service Engineer (TSE) provides the clinical and technical interface between the medical community and the various Cardiac Rhythm Management departments through consultation. Work requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more biomedical engineering or other medical-related academic course of study. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. Stays abreast of and consults on technical advancements. Promotes the process of continuous quality improvement and risk management, and coordinates solutions for technical and project issues. Exercises judgment in planning and organizing work; monitors performance and reports status.\n\nRequirements/Education: Requires a Bachelors Degree in electronic engineering, biomedical engineering, a related field, or equivalent. Typically a minimum of two plus years of work experience providing medical device industry technical support, including relevant experience in the cardiac pacing industry. Requires the demonstrated ability to analyze and evaluate technologically complex devices; demonstrated written and verbal communication, interpersonal, facilitation, presentation, quantitative, analytical, organizational, multi-task, and follow-up skills, the ability to meet deadlines as well as the ability to converse effectively with all levels of employees, management and customers. Must be able to meet deadlines on multiple projects/assignments. Must also be able to establish/maintain good working relationships and be able to work cooperatively/productively with engineers, vendors, customers, and Field Clinical Engineers is required. Demonstrated ability to understand and comply with applicable U.S. Food and Drug Administration (FDA) regulations and Company operating procedures, processes, policies, and tasks. Demonstrated personal computer skills including spreadsheet, word processing, database management, and specialized applications. Evaluation, originality, and/or ingenuity required.\n\nDesired Requirements: Biomedical Engineering background. Knowledge of cardiac anatomy/physiology and cardiac pacing/defibrillation systems from a clinical and technological perspective is desired. A demonstrated understanding of electrocardiograms is also preferred.\n\nCandidate that can work in a fast-paced environment, with attention to detail, meet deadlines, and has excellent organizational skills. Knowledge in FDA CDRH regulations a plus.\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-04-12 01:39:32", "url": "http://jobs.sjm.com/xml/27828034/job", "country": "United States", "company": "St. Jude Medical", "title": "Technical Service Engineering Specialist", "reqid": "12699", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 27828034}, {"country_short": "USA", "city": "Sunnyvale", "description": "Engineer, Principal Human Factors Design\nJob Requisition #: 12779\nDate Posted: 04/10/2012\nCategory: Engineering\nLocation: Sunnyvale - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management business unit, located in Sunnyvale, CA:\n\nJob Overview\nEngineer, Prin Human Fact Design\n\nSummary Working independently without appreciable managerial oversight and direction, creates, develops, and leads teams that execute human factors engineering process for critically important products and product lines with the purpose of meeting divisional growth objectives. Plans, leads and conducts customer and competitive research to identify, prioritize/develop new projects, create detailed usability improvement plans, conceptual design, select/manage external usability design resources, and lead internal and external development resources to conduct customer usability research, conceptual design development, usability testing, interaction design and usability validation. In addition, is responsible for usability initiatives across product/organizational lines, and for training staff members about relevant usability theory, resources, and technology. Primarily supports one or multiple major programs and may advise other multiple efforts. Considered the Human Factors Departments technical product or protocol expert. Applies theoretical principles and analytical techniques normally acquired in a recognized four-year or more of academic studies. Identifies and routinely uses the most effective, cost efficient and best business practices to execute processes; continually evaluates their effectiveness and appropriateness. Applies advanced usability improvement principles to the evaluation and solution of complex product design problems. Remains abreast of and consults on usability improvement advancements. Creates and trains others in the use of the most effective, cost efficient and best usability related processes; continually evaluates their effectiveness and appropriateness. Exercises independent judgment in the planning, organizing and performing work; monitors own and project teams performance and reports status to management and program team. Assures that quality of services meets or exceeds internal and external customer requirements.\nQualifications Requirements/Education: Bachelors Degree in Psychology, Human Factors, Engineering, and Marketing, a related field, or equivalent. Typically a minimum of ten plus years of progressively more responsible work experience with the design of software for complex applications. Requirements include an in-depth knowledge and experience of: human factors as well as cognitive psychology theory and application; the software development process, software technology, and effective methods of working with research & development teams; customers, trends, governmental factors and emerging research and technologies affecting product usability. A qualified record of implementing new processes to existing human factors and related systems. Requires comprehensive written and verbal communication, interpersonal, facilitation, presentation, quantitative, analytical, organizational, and follow-up skills, the ability to meet deadlines on multiple projects as well as the ability to converse effectively with all levels of employees. Documented record of delivering software engineering information which adds value to managements decision making process. Demonstrated ability to understand and comply with applicable U.S. Food & Drug Administration (FDA) regulations and Company operating procedures, processes, policies, and tasks. Advanced personal computer skills including spreadsheet, word processing database management, and specialized applications. Must be able to handle multiple assignments. Must be able to perform in a diverse cross-functional team environment. Desired Requirements: An advanced credential in human factors engineering, cognitive or experimental psychology, or in a field related to human-computer interaction. Experience with the cardiac pacing and defibrillation device market is also highly desirable. Academic or in-house courses in project management, leadership, training, continuous improvement (CI), and various technical applications as noted above.\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-04-12 01:39:24", "url": "http://jobs.sjm.com/xml/27828016/job", "country": "United States", "company": "St. Jude Medical", "title": "Engineer, Principal Human Factors Design", "reqid": "12779", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 27828016}, {"country_short": "USA", "city": "Sunnyvale", "description": "Engineering Group Leader\nJob Requisition #: 12375\nDate Posted: 04/11/2012\nCategory: Tachy Product Development\nLocation: Sunnyvale - CA - USA\nSylmar - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management Division (CRMD):\n\nJob Overview\nWe are seeking a hands-on highly technical Engineering Group Leader to directly work on and lead a small team of engineers on RF characterization from IC to system level on implantable biomedical products.  These implantable pacemakers and implantable defibrillators save lives and provide therapy for serious medical conditions.\n\nOur devices are complex, low-power, embedded systems and include custom analog, digital, and mixed signal ICs, hybrids, and discrete components. The successful person in this role will have a strong RF background including hands-on RF characterization and leadership skills.\n\nThe group lead will play a key role in growing our RF characterization capabilities and setting the example of comprehensive analysis of design, creation of appropriate characterization test plans with rationale for choices, critical evaluation of results, and trouble-shooting.  This person will work closely with other cross-functional groups such as Design, ATE, Firmware, Clinical Systems, Manufacturing, and Program Management.\n\nRequired Skills:\n\n\u2022 MSEE with at least 3 years or BSEE with at least 5 years of RF systems experience\n\u2022 Theoretical and practical understanding of RF at system level\n\u2022 Hands on RF characterization including use of RF bench equipment\n\u2022 Experience leading / mentoring engineers in RF characterization\n\u2022 Strong technical analysis and troubleshooting skills for products containing RF, analog / digital ICs, discrete components, embedded systems\n\u2022 Excellent interpersonal and communication skills with ability to multi-task\n\u2022 Track record working collaboratively across functions in successful product development\n\u2022 Demonstrated ability to organize, analyze, document, prepare for characterization test plans, reviews, and reports\n\u2022 Ability to pick things up quickly\n\u2022 Motivated to learn about and ability to lead biomedical product development\n\u2022 Recruiting and team building\n\nDesired Skills:\n\n\u2022 RF IC and RF Systems experience including ATE and bench equipment\n\n\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-04-12 01:38:12", "url": "http://jobs.sjm.com/xml/27827357/job", "country": "United States", "company": "St. Jude Medical", "title": "Engineering Group Leader", "reqid": "12375", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 27827357}, {"country_short": "USA", "city": "Sunnyvale", "description": "Engineer I, Software\nJob Requisition #: 12774\nDate Posted: 04/04/2012\nCategory: Software\nLocation: Sunnyvale - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management business unit, located in the suburbs of Los Angeles:\n\nJob Overview\nWorking under general supervision, performs specialized level software project activities in such areas as Development Engineering, IT Engineering, System Engineering, Test Engineering, and/or related areas. Assignments may include, but are not limited to, analyzing requirements and providing strategic feedback, planning and scheduling data, updating and maintaining different software specifications based on analysis of specifications, needs and improvements, as well as troubleshooting, debugging, and maintaining of software, test, or tool designs, cases, scripts, procedures, and/or code based on strategic analysis. Work requires the application of theoretical engineering principles, evaluation, ingenuity and creative/analytical techniques typically acquired in a recognized four-year or more academic course of specialized study.\n\n\u2022 Exposure to writing requirements\n\u2022 Exposure to embedded software\n\u2022 Knowledge of basic electronics, hardware design, and cardiovascular physiology\n\u2022 Knowledge of pacemaker and/or ICD algorithms a plus\n\u2022 Experience with DOORS and ClearQuest a plus\n\u2022 Team leadership skills including, but not limited to, resource planning and employee mentorship a plus\n\u2022 Ability to comfortably work in an FDA-regulated environment as part of a team with clear, well-defined processes\n\u2022 Someone who is high-energy, enthusiastic, and looking to make a significant contribution to the organization\n\u2022 Someone who is extremely meticulous (detail-oriented)\n\nRequirements/Education: Bachelor of Science Degree in Computer Science Engineering or a related engineering field. A minimum of six months of relevant software engineering work experience on multiple platforms with varied programming methods is required. Requires demonstrated written and verbal communication, interpersonal, analytical, organizational, and follow-up skills, the ability to meet deadlines as well as the ability to converse effectively with all levels of employees. Must be able to handle multiple assignments. Must be able to perform in a diverse cross-functional team environment. Demonstrated ability to understand and comply with applicable U.S. Food and Drug Administration (FDA) regulations and Company operating procedures, processes, policies, and tasks. Must have demonstrated personal computer skills, be able to perform basic word processing/spreadsheet tasks to perform documentation, presentation, and analysis activities and be able to grasp new technical concepts and tools quickly. Evaluation, originality, and/or ingenuity required.\n\nDesired Requirements: Relevant coursework and/or a demonstrated understanding of product development/clinical engineering concepts, theory, and applications are desired. Relevant coursework and/or a demonstrated understanding of cardiac electro-physiology. The demonstrated ability to effectively integrate information from varied disciplines including Clinical Medicine, Engineering, Marketing, as well as Regulatory Affairs is also desired. Previous experience in the implantable medical device industry is preferred.\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-04-04 20:00:40", "url": "http://jobs.sjm.com/xml/27644376/job", "country": "United States", "company": "St. Jude Medical", "title": "Engineer I, Software", "reqid": "12774", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 27644376}, {"country_short": "USA", "city": "Sunnyvale", "description": "Senior Software Verification Engineer (C++, C#)\nJob Requisition #: 12829\nDate Posted: 04/04/2012\nCategory: Software\nLocation: Sunnyvale - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management business unit, located in Sunnyvale, CA:\n\nJob Overview\nPlease only apply if you have 5+ years software verification with C++ and C#. Stable work history is a must too.\n\nWorking without appreciable supervision, performs moderate risk/highly complex software project activities in such areas as SW Development and/or automated software Testing. Assignments may include, but are not limited to, the designing, developing, updating, and maintaining of different software test specifications or test libraries as well as the troubleshooting, debugging, and maintenance of software test code or test library code at a multiple sub-systems or application levels. Assignments may also include capturing, gathering, analyzing, maintaining, and validating applicable product or software requirements. Work requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more academic course of study. Applies advanced engineering and scientific principles to the evaluation and solution of technical problems. Initiates the planning, organizing, performing, coordinating and/or directing of engineering work. Performs technical studies. Remains abreast of and consults on technical advancements. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness.\n\nRequirements/Education: Bachelors Degree in Computer Science, a related field, or equivalent. Typically a minimum of six plus years of progressively more responsible work experience in a range of software engineering disciplines using a variety of programming methods. Broad cross-disciplinary and in-depth knowledge of the software engineering profession. A comprehensive familiarity with commodity/off-the-shelf software tools, and programs. A qualified record of implementing new processes to existing software and related systems. Requires comprehensive written and verbal communication, interpersonal, facilitation, presentation, quantitative, analytical, organizational, follow-up skills, and the ability to meet deadlines on multiple projects as well as the ability to converse effectively with all levels of employees. A documented record of delivering software engineering information which adds value to managements decision making process is required. A demonstrated ability to understand and comply with applicable FDA regulations and Company operating procedures, processes, policies, and tasks is also required. Advanced personal computer skills including spreadsheet, word processing database management, and specialized applications. Must be able to handle multiple assignments. Must be able to perform in a diverse cross-functional team environment.\n\nRequired:\nProficiency and/or work experience designing and implementing automated software testing is required. Proficiency and/or work experience in software utilizing a variety of programming languages such as C++, and/or C# are required. Strong written/verbal communication, analytical thinking, and problem solving skills are desired. Proficiency and/or work experience with object-oriented methodology including analysis, design, development, and structured software development is desired.\n\nDesired Requirements: An advanced credential in a relevant discipline/concentration. Specialized experience and/or relevant coursework related to the software applications, programs, and processes. Academic or in-house courses in project management, leadership, training, and various technical applications as noted above.\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-04-04 20:00:13", "url": "http://jobs.sjm.com/xml/27644368/job", "country": "United States", "company": "St. Jude Medical", "title": "Senior Software Verification Engineer (C++, C#)", "reqid": "12829", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 27644368}, {"country_short": "USA", "city": "Sunnyvale", "description": "Server Administrator\nJob Requisition #: 12735\nDate Posted: 04/04/2012\nCategory: Information Technology\nLocation: Sunnyvale - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management business unit, located in Sunnyvale, CA:\n\nJob Overview\nWorking under general supervision, oversees and coordinates overall activities relating to the operation and maintenance of computer servers and the installation and configuration of new computer equipment. . Executes activities relating to the operation and maintenance of computer systems including monitoring, backups, installation, configuration and operation of new and existing IT equipment. The position will also include support of Client PC\u2019s, responsible for the installation, repair and preventative maintenance of personal computers (PCs), networks and related systems. Performs all installations, configurations, upgrades and backups of software (i.e., Microsoft Office, Windows OS) and hardware applications at end user locations. Troubleshoots software and hardware failures and identifies network problems when they relate to PCs.\n\nQualifications:\nRequirements/Education: Requires a Bachelors Degree in Computer Science or equivalent. Typically a minimum of four years technical experience in computer maintenance and repair including at least two years direct experience in the systems management and administration of a medium to large computer server and client environments supporting at least 200 users. Formal training in computer systems management and administration is also required. Demonstrated oral and written interpersonal, communication, analytical, presentation, and organizational skills; the ability to meet deadlines/work independently. Must be adept at handling multiple assignments in a timely manner and meeting assigned deadlines. Desired Requirements: A relevant advanced degree and/or appropriate professional certification, i.e., Microsoft Certified Systems Engineer (MSCE).\n\nSpecific Job Skill:\nSolid experience required with Windows OS, VMware, MS Applications, Software Deployment Tools, and Desktop troubleshooting tools. Broad cross-disciplinary perspective with demonstrated competency in two or more of key IT technologies (e.g., server operating systems, virtualization, network, storage/SAN, system backups, security, Client desktop support, Software deployment) This would also include training in deskside automation support and/or service. Must have demonstrated personal computer application (e.g., spreadsheet and word processing), installation and repair skills. Must possess advanced computer skills including a working familiarity with system management tools and utilities, spreadsheets and document applications, communication tools, and other directly relevant applications. The ability to work independently. The demonstrated ability to understand and comply with applicable government regulations and Company operating procedures, processes, policies and rules is essential. Must be able to operate in a diverse cross-functional team environment. Must be able to maintain regular and predictable attendance; the ability work overtime is also required.\n\nMust be a team player with excellent oral and written communication skills.\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-04-04 19:59:50", "url": "http://jobs.sjm.com/xml/27644362/job", "country": "United States", "company": "St. Jude Medical", "title": "Server Administrator", "reqid": "12735", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 27644362}, {"country_short": "USA", "city": "Sunnyvale", "description": "Engineer I, Design Assurance\nJob Requisition #: 12632\nDate Posted: 03/27/2012\nCategory: Quality Assurance\nLocation: Sunnyvale - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management business unit, located in Sunnyvale, CA:\n\nJob Overview\nSummary  Working under close supervision on defined work assignments and/or usually following established procedures, supports the qualification testing of potential new products, accessories and components. Performs failure investigations on electrical circuits and subassemblies. Work requires the application of theoretical principles, evaluation, ingenuity, and creative/analytical techniques typically acquired in a recognized four-year or more academic course of study. Applies engineering and scientific principles to the evaluation and solution of technical problems. Exercises basic technical judgment in planning, organizing, performing, and/or coordinating engineering work. Stays abreast of and communicates technical advancements to colleagues and associates. Routinely uses the most effective, cost efficient and best practices to execute processes.\n\nQualifications  Requirements/Education: Bachelor\u2019s Degree in Engineering (e.g., Electrical, Mechanical, etc.), or in a physical science, a related field, or equivalent including relevant coursework and/or work experience in the design assurance profession. Requires demonstrated written and verbal communication, interpersonal, analytical, organizational, and follow-up skills, the ability to meet deadlines as well as the ability to converse effectively with all levels of employees. Must be able to handle multiple assignments. Must be able to perform in a diverse cross-functional team environment. Must have the demonstrated ability to understand and comply with applicable U.S. Food and Drug Administration (FDA) regulations and Company operating procedures, processes, policies, and tasks. Must have demonstrated personal computer skills and be able to perform basic word processing/spreadsheet tasks to perform documentation, presentation, and analysis activities. Desired Requirements: Prefer a degree in Electrical or Biomedical Engineering, experience in troubleshooting/failure analysis, specialized training, relevant coursework and/or a demonstrated understanding of design assurance engineering concepts, theory, and applications are desired. Experience in the implantable medical device industry.\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-03-27 20:24:08", "url": "http://jobs.sjm.com/xml/27424323/job", "country": "United States", "company": "St. Jude Medical", "title": "Engineer I, Design Assurance", "reqid": "12632", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 27424323}, {"country_short": "USA", "city": "Sunnyvale", "description": "Technical Service Engineering Specialist\nJob Requisition #: 12713\nDate Posted: 03/27/2012\nCategory: Technical Services\nLocation: Sunnyvale - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management business unit, located in Sunnyvale, CA:\n\nJob Overview\nFunctioning under general supervision in accordance with established policies/procedures, provides independent clinical and technical support in response to inquiries from physicians, health care professionals, patients and field staff using professional knowledge and judgment. This level of the Technical Service Engineer (TSE) provides the clinical and technical interface between the medical community and the various Cardiac Rhythm Management departments through consultation. Work requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more biomedical engineering or other medical-related academic course of study. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. Stays abreast of and consults on technical advancements. Promotes the process of continuous quality improvement and risk management, and coordinates solutions for technical and project issues. Exercises judgment in planning and organizing work; monitors performance and reports status.\n\nRequirements/Education: Requires a Bachelors Degree in electronic engineering, biomedical engineering, a related field, or equivalent. Typically a minimum of two plus years of work experience providing medical device industry technical support, including relevant experience in the cardiac pacing industry. Requires the demonstrated ability to analyze and evaluate technologically complex devices; demonstrated written and verbal communication, interpersonal, facilitation, presentation, quantitative, analytical, organizational, multi-task, and follow-up skills, the ability to meet deadlines as well as the ability to converse effectively with all levels of employees, management and customers. Must be able to meet deadlines on multiple projects/assignments. Must also be able to establish/maintain good working relationships and be able to work cooperatively/productively with engineers, vendors, customers, and Field Clinical Engineers is required. Demonstrated ability to understand and comply with applicable U.S. Food and Drug Administration (FDA) regulations and Company operating procedures, processes, policies, and tasks. Demonstrated personal computer skills including spreadsheet, word processing, database management, and specialized applications. Evaluation, originality, and/or ingenuity required.\n\nDesired Requirements: Biomedical Engineering background. Knowledge of cardiac anatomy/physiology and cardiac pacing/defibrillation systems from a clinical and technological perspective is desired. A demonstrated understanding of electrocardiograms is also preferred.\n\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-03-27 20:23:10", "url": "http://jobs.sjm.com/xml/27424287/job", "country": "United States", "company": "St. Jude Medical", "title": "Technical Service Engineering Specialist", "reqid": "12713", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 27424287}, {"country_short": "USA", "city": "Sunnyvale", "description": "Technical Service Engineering Specialist\nJob Requisition #: 12621\nDate Posted: 03/15/2012\nCategory: Quality\nLocation: Sunnyvale - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management business unit, located in Sunnyvale, CA:\n\nJob Overview\nFunctioning under general supervision in accordance with established policies/procedures, provides independent clinical and technical support in response to inquiries from physicians, health care professionals, patients and field staff using professional knowledge and judgment. This level of the Technical Service Engineer (TSE) provides the clinical and technical interface between the medical community and the various Cardiac Rhythm Management departments through consultation. Work requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more biomedical engineering or other medical-related academic course of study. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. Stays abreast of and consults on technical advancements. Promotes the process of continuous quality improvement and risk management, and coordinates solutions for technical and project issues. Exercises judgment in planning and organizing work; monitors performance and reports status.\n\nRequirements/Education: Requires a Bachelors Degree in electronic engineering, biomedical engineering, a related field, or equivalent. Typically a minimum of two plus years of work experience providing medical device industry technical support, including relevant experience in the cardiac pacing industry. Requires the demonstrated ability to analyze and evaluate technologically complex devices; demonstrated written and verbal communication, interpersonal, facilitation, presentation, quantitative, analytical, organizational, multi-task, and follow-up skills, the ability to meet deadlines as well as the ability to converse effectively with all levels of employees, management and customers. Must be able to meet deadlines on multiple projects/assignments. Must also be able to establish/maintain good working relationships and be able to work cooperatively/productively with engineers, vendors, customers, and Field Clinical Engineers is required. Demonstrated ability to understand and comply with applicable U.S. Food and Drug Administration (FDA) regulations and Company operating procedures, processes, policies, and tasks. Demonstrated personal computer skills including spreadsheet, word processing, database management, and specialized applications. Evaluation, originality, and/or ingenuity required.\n\nDesired Requirements: Biomedical Engineering background. Knowledge of cardiac anatomy/physiology and cardiac pacing/defibrillation systems from a clinical and technological perspective is desired. A demonstrated understanding of electrocardiograms is also preferred.\n\nCandidate that can work in a fast-paced environment, with attention to detail, meet deadlines, and has excellent organizational skills. Knowledge in FDA CDRH regulations a plus.\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-03-15 21:38:22", "url": "http://jobs.sjm.com/xml/27178514/job", "country": "United States", "company": "St. Jude Medical", "title": "Technical Service Engineering Specialist", "reqid": "12621", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 27178514}, {"country_short": "USA", "city": "Sunnyvale", "description": "Clinical Product Surveillance (CPS) Analyst\nJob Requisition #: 12524\nDate Posted: 02/22/2012\nCategory: Clinical\nLocation: Sunnyvale - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management business unit, located in Sunnyvale, CA:\n\nJob Overview\nWorking under the general direction of the department manager while demonstrating a high degree of discretion and independent judgment, is accountable for the professional medical analysis and validation of product surveillance documents, medical device reports (MDRs), and customer letters. Analyzes customer inquiries to ensure company responses are medically appropriate and include relevant, accurate, and thorough technical, clinical, and educational information while communicating directly with the customer. Makes recommendations to management based on these analyses. Reviews and validates product surveillance documents and medical device reports for patient safety and product efficacy. Stays abreast of and communicates developments to ensure that product surveillance files comply with U.S. Food and Drug Administration (FDA) regulations as well as company policy.\n\nRequirements/Education: Bachelors of Science Degree in Nursing (BSN) and a current nursing license or BME degree. A minimum of four plus years of relevant experience in clinical risk analysis/or technical support in the cardiac pacing industry, or equivalent. Candidate must demonstrate strong written and oral communication skills. Demonstrated ability to understand, interpret, and comply with US Food and Drug Administration (FDA) regulations and Company operating procedures. Must be able to demonstrate the ability to read and interpret medical reports as well as product documentation. Candidate must possess demonstrated organizational skills, professional and business judgment, sound decision-making and problem-solving abilities, discretion, and excellent organizational skills for managing multiple ongoing tasks. Candidate must be able to meet deadlines on multiple projects. Must be detail- and team-oriented and be able to function independently in a busy department while working with cross-functional teams and providing support to other team members. Must possess demonstrated personal computer literacy and proficiency with standard software applications, including Excel, Word or equivalent applications are required. Must be able to demonstrate the ability to read and interpret medical reports as well as product documentation.\n\nDesired Requirements: An advanced degree in a relevant discipline. Knowledge of cardiac anatomy/physiology and/or cardiac pacing/defibrillation systems from a clinical perspective is desired. RN with background in Cardiac Electrophysiology is preferred.\n\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2012-02-22 22:00:35", "url": "http://jobs.sjm.com/xml/26691993/job", "country": "United States", "company": "St. Jude Medical", "title": "Clinical Product Surveillance (CPS) Analyst", "reqid": "12524", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 26691993}, {"country_short": "USA", "city": "Sunnyvale", "description": "Quality Technician\nJob Requisition #: 12039\nDate Posted: 12/14/2011\nCategory: Technician\nLocation: Sunnyvale - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management business unit, located in Sunnyvale, CA:\n\nJob Overview\nWorking under general supervision, provides quality inspection and support services as required by Company quality provisions. Takes initiative to ensure work is done accurately and completely. Performs assignments of moderate complexity. Applies existing work methods to different known situations. Problems involve recurring, routine situations; usually refers more complex problems to supervisor or more senior level personnel within the Quality organization.\n\nRequirements/Education: High School diploma or equivalent. A minimum of four or more years related experience in quality/inspection activities. Demonstrated knowledge and understanding of all aspects of the job, including common inspection methods. Demonstrated ability to use frequently used hand tools. Demonstrated verbal and written communication, interpersonal, organizational and basic math skills. Demonstrated ability to read and understand engineering drawings. Must be able to maintain regular and predictable attendance; the ability work overtime is also required.\n\nDesired Requirements: 1-2 years of experince. An Associates degree in Electrical/Mechanical Technology, equivalent trade school/military training, or comparable related experience in biomedical field. Prior experience working in an air-conditioned clean-room manufacturing environment.\n\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2011-12-14 23:10:48", "url": "http://jobs.sjm.com/xml/25361322/job", "country": "United States", "company": "St. Jude Medical", "title": "Quality Technician", "reqid": "12039", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 25361322}, {"country_short": "USA", "city": "Sunnyvale", "description": "Sr. Software Development Engineer\nJob Requisition #: AF13676\nDate Posted: 12/12/2011\nCategory: Software\nLocation: Sunnyvale - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Atrial Fibrillation Division.\n\nJob Overview\nWe are seeking an experienced, high caliber Senior Software Engineer to meet our standard product development needs as well as increase our ability to deliver integrated hardware and software solutions to meet our project specific requirements.\n\nImpact this role will have within the AF division:\n\u2022 The Senior R&D Software Engineer designs and develops application software for RF ablation systems.\n\u2022 This role writes product requirement documents, designs, develops code, unit tests and helps out the verification team.\n\nRequired Qualifications:\n\u2022 Bachelor\u2019s degree in Computer Science, Computer or Electrical Engineering\n\u2022 7 + years hands-on development experience with real-time embedded hardware, software design and development, and programming experience in C/C++, QT, Object Oriented programming with knowledge of Hardware interfaces and microprocessors\n\u2022 Experience with Linux, or other real time operation system, OS kernel module, device driver development\n\u2022 Familiarity with software configuration and software defect tracking systems\n\u2022 Demonstrated ability to understand and comply with applicable FDA regulations and Company operating procedures, processes, policies, and tasks\n\u2022 Effective verbal and written communication skills to interact with associates at all levels of the organization, vendors and other SJM entities\n\u2022 Adaptability to frequent change in the work environment\n\u2022 Ability to prioritize responsibilities and ensure deadlines are met\n\u2022 Proficient working knowledge of MS Word, Outlook, PowerPoint, Excel and Project\n\u2022 Experience with 3D image processing, registration and rendering software design, Wireless protocols\n\u2022 Polished communicator- written documentation and oral presentations/ discussions/ meetings\n\u2022 Excellent reputation for building relationships across various levels of an organization.\n\u2022 Organized, on-time, and detailed project management skills.\n\u2022 Energized attitude.\n\nPreferred Qualifications:\n\u2022 Masters degree in Computer Science, Computer or Electrical Engineering\n\u2022 Experience with RTOS, debugging tools and good software development processes\n\u2022 Working knowledge of entire software development and test cycle with at least one complete FDA regulated medical device product development cycle. Knowledge of applicable international regulations and standards (QSR, ISO 13485, ISO14971)\n\u2022 Formal training in Program/Project Management or Program Management Professional Certification\n\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2011-12-12 21:45:19", "url": "http://jobs.sjm.com/xml/25308317/job", "country": "United States", "company": "St. Jude Medical", "title": "Sr. Software Development Engineer", "reqid": "AF13676", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 25308317}, {"country_short": "USA", "city": "Sunnyvale", "description": "Biostatistician\nJob Requisition #: 11977\nDate Posted: 11/30/2011\nCategory: Clinical\nLocation: Sunnyvale - CA - USA\nSylmar - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management Division (CRMD):\n\nJob Overview\nAccountable to provide statistical input into the design of clinical studies, investigational plans, case report forms, database setup, edit checks, and clinical reports.  Also responsible for providing consulting services to departments other than Clinical Affairs. Monitors own work performance and reports status to management. Coordinates technical decisions across organizational lines. Remains abreast of and consults on biostatistical and related advancements. Assures that quality of services meets or exceeds internal customer requirements.\n\nRequirements/Education: Masters of Science degree Biostatistics with 3 years experience of PhD in Biostatistics with 1-2 years experience. Prefer exposure to medical device industry. Requirements include an expert knowledge and experience of: computer science; biostatistical theory and application; and effective methods of working with clinical teams. Requires comprehensive written and verbal communication, interpersonal, facilitation, presentation, quantitative, analytical, organizational, and follow-up skills, the ability to meet deadlines on multiple projects as well as the ability to converse effectively with all levels of employees. Documented record of delivering biostatistical information which adds value to managements decision making process. Demonstrated ability to understand and comply with applicable FDA regulations and Company operating procedures, processes, policies, and tasks. Advanced personal computer skills including spreadsheet, word processing database management, and specialized statistical software packages with an emphasis on strong skills using Statistical Analysis System (i.e., SAS) software. Must be able to handle multiple assignments. Must be able to perform in a diverse cross-functional team environment.\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2011-11-30 23:14:47", "url": "http://jobs.sjm.com/xml/25120522/job", "country": "United States", "company": "St. Jude Medical", "title": "Biostatistician", "reqid": "11977", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 25120522}, {"country_short": "USA", "city": "Sunnyvale", "description": "Biostatistician\nJob Requisition #: 11855\nDate Posted: 11/08/2011\nCategory: Clinical\nLocation: Sunnyvale - CA - USA\nSylmar - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management Division (CRMD):\n\nJob Overview\nAccountable to provide statistical input into the design of clinical studies, investigational plans, case report forms, database setup, edit checks, and clinical reports.  Also responsible for providing consulting services to departments other than Clinical Affairs. Monitors own work performance and reports status to management. Coordinates technical decisions across organizational lines. Remains abreast of and consults on biostatistical and related advancements. Assures that quality of services meets or exceeds internal customer requirements.\n\nRequirements/Education: Masters of Science degree Biostatistics with 3 years experience of PhD in Biostatistics with 1-2 years experience. Prefer exposure to medical device industry. Requirements include an expert knowledge and experience of: computer science; biostatistical theory and application; and effective methods of working with clinical teams. Requires comprehensive written and verbal communication, interpersonal, facilitation, presentation, quantitative, analytical, organizational, and follow-up skills, the ability to meet deadlines on multiple projects as well as the ability to converse effectively with all levels of employees. Documented record of delivering biostatistical information which adds value to managements decision making process. Demonstrated ability to understand and comply with applicable FDA regulations and Company operating procedures, processes, policies, and tasks. Advanced personal computer skills including spreadsheet, word processing database management, and specialized statistical software packages with an emphasis on strong skills using Statistical Analysis System (i.e., SAS) software. Must be able to handle multiple assignments. Must be able to perform in a diverse cross-functional team environment.\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2011-11-08 20:41:09", "url": "http://jobs.sjm.com/xml/24757508/job", "country": "United States", "company": "St. Jude Medical", "title": "Biostatistician", "reqid": "11855", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 24757508}, {"country_short": "USA", "city": "Sunnyvale", "description": "Director, ATE\nJob Requisition #: 11370\nDate Posted: 07/25/2011\nCategory: ATE\nLocation: Sunnyvale - CA - USA\nSylmar - CA - USA\n\n\nAbout Us\nOur teams produce game-changing ideas and life-changing results. A career at St. Jude Medical puts you on the leading edge of medical technology, working for a company driven by its entrepreneurial culture and its passion for quality. Isn't this the kind of change you would like in your life?\n\n\n\nWe are an Equal Opportunity/Affirmative Action Employer. We currently have this position open at our Cardiac Rhythm Management Division (CRMD):\n\nJob Overview\nJoin the Cardiac Rhythm Management Division's Automated Test Engineering group. We are one of the world's leaders in the life-saving field implantable cardiac rhythm management devices, and we are looking to get even better by bringing on the world's best engineering talent!\n\nAs a manager in the test engineering group, you will plan and manage all areas within test development. Your team will be involved in product development, design for testability, test hardware and software design, hands-on debug, characterization, manufacturing release and sustaining.\n\nYou will manage 5 to 20 engineers and technicians, with analog, mixed-signal and digital technical focus. You may be involved in wafer level IC test development, test development for partial system assemblies, or device level test of the final product.\n\nYou will be in charge of a key engineering function in the company's largest business division.\n\nRequirements:\n\nBSEE or MSEE\n\n10+ years experience in analog or mixed-signal test development\n\n5+ years managing test engineers\n\n\"Hands-on\". Technically savvy, especially with analog and mixed-signal circuits\n\nExcellent communication skills. Masterful at avoiding miscommunication, providing clear expectations.\n\nFocused and able to meet goals\n\n\n\n|E-mail this position \nSubmit Resume or C.V.", "date_new": "2011-07-25 18:20:57", "url": "http://jobs.sjm.com/xml/22602291/job", "country": "United States", "company": "St. Jude Medical", "title": "Director, ATE", "reqid": "11370", "state": "California", "state_short": "CA", "location": "Sunnyvale, CA", "uid": 22602291}]