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Job description:
Requirements:
Perks & Benefits
職位描述：
要求：
獲得認可大學的醫學學士學位或醫學學位。
已在馬來西亞醫學理事會註冊。
擁有年度執業認證（APC）。
至少 6 年工作經驗。
打扮得體，個性開朗。
優秀的人際溝通、溝通和領導能力。
願意在新山工作。
津貼和福利
Key Responsibilities:
Requirements:
Perks & Benefits
Welcome to Dee Noon Corporation Sdn Bhd, a distinguished furniture manufacturer and exporter nestled in the scenic locale of Sungai Baong, Penang. Since our establishment in May 2006, we have been dedicated to crafting exquisite furniture pieces that embody both quality and style.
At Dee Noon Corporation, we take pride in our diverse product range, which spans Bedroom Furniture, Living Room Furniture, Kitchen Furniture, Children's Furniture, and more. With an extensive global reach, our products grace homes in approximately 30 countries, including prestigious markets such as Japan, the United States, the United Kingdom, the Middle East, Europe, South East Asia, and South Africa.
Setting the bar high, we boast a remarkable production capacity of around 90 containers per month. Committed to excellence, we adhere to the rigorous standards of ISO 9001:2015, ensuring that every piece of furniture we produce meets the highest quality benchmarks, consistently surpassing customer expectations.
Our success story is a testament to the dedication of our dynamic management team, comprising 31 skilled professionals, and a workforce of approximately 305 individuals. Through strategic expansions into different plants and diversified product ranges, we continue to grow, innovate, and redefine the standards of the furniture manufacturing industry.
主要責任：
要求：
津貼和福利
Welcome to Dee Noon Corporation Sdn Bhd, a distinguished furniture manufacturer and exporter nestled in the scenic locale of Sungai Baong, Penang. Since our establishment in May 2006, we have been dedicated to crafting exquisite furniture pieces that embody both quality and style.
At Dee Noon Corporation, we take pride in our diverse product range, which spans Bedroom Furniture, Living Room Furniture, Kitchen Furniture, Children's Furniture, and more. With an extensive global reach, our products grace homes in approximately 30 countries, including prestigious markets such as Japan, the United States, the United Kingdom, the Middle East, Europe, South East Asia, and South Africa.
Setting the bar high, we boast a remarkable production capacity of around 90 containers per month. Committed to excellence, we adhere to the rigorous standards of ISO 9001:2015, ensuring that every piece of furniture we produce meets the highest quality benchmarks, consistently surpassing customer expectations.
Our success story is a testament to the dedication of our dynamic management team, comprising 31 skilled professionals, and a workforce of approximately 305 individuals. Through strategic expansions into different plants and diversified product ranges, we continue to grow, innovate, and redefine the standards of the furniture manufacturing industry.
We are the makers of possible
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.
Why Join Us?
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
Become a maker of possible with us!
The R&D Senior Packaging Engineer will be a part of the newly formed Sustainability Center of Excellence (COE) located in BD Singapore. The Sustainability COE is modeled after the Sustainable Medical Technology Institute (SMTI) and will have the same mandate as the SMTI. In this role, the Senior Packaging Engineer will be responsible for execution of the broader R&D Sustainability strategy at BD. This individual will help integrate sustainability focus into programs for making changes to current products and to new product development programs in all 8 BD businesses. In particular, this individual will support Design for Sustainability efforts within BD’s R&D portfolio. This will require ability on the candidate’s part to work cross-functionally and with different stakeholders across geographies. Some travel may be required.
This is a critical role in the COE and this individual will drive activities focused on assessing and reducing the carbon footprint of BD products. The long-term vision is to have environmental sustainability become an integral part of the product and packaging development process, and the work done by him /her will be instrumental in enabling this outcome. He / she will strike a balance of fast-paced execution with thoroughness of approach, using iterative concept development informed by stakeholder feedback.
The R&D Senior Packaging Engineer supports design, development, and validation of medical device packaging. The successful candidate will contribute to and/or lead a portfolio of packaging projects and ensure that best practices are employed and will have the opportunity to develop as an internal subject matter expert with respect to fundamental packaging materials and design. This includes test method development and alignment to existing and evolving global standards governing packaging.
This position will be accountable for supporting medium to high complexity projects, products, systems, or services within BD. Regular interaction and collaboration with R&D and project team members within each Business Unit is critical for the successful execution of responsibilities.
Job Description
Preferred Requirements
Click on apply if this sounds like you!
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.
To learn more about BD visit: https://bd.com/careers
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Senior R&D Manager, Medical Imaging Applications (Plymouth, MN)
As a key member of the Image Guided Therapy-Devices (IGT-D) R&D software management team you will lead an R&D team that drives the full product development lifecycle of clinical application for our intravascular ultrasound (IVUS) SW platform.
Your role:
Lead a software department to develop and deliver differentiated clinical software applications that radically improve ease-of-use of intravascular ultrasound (IVUS) and hemodynamic diagnostic devices through x-ray and device co-registration and application of artificial intelligence strategies in both coronary vascular and peripheral vascular procedures. Learn more here, IntraSight
Attract, retain, and develop top-talent in one the fastest growing businesses in Philips.
Crates an engaged, innovative, and inspiring working environment by motivating, challenging, and coaching the department's employees towards professional growth, manages and optimizes the innovative climate, stimulates entrepreneurship and drives engagement.
Collaborate with other functional leaders inside and outside of R&D to drive business results to ensure great customer digital solutions are developed. Learn more by hearing from our physician partners.
You're the right fit if:
10 years’ experience developing high-tech applications in C++.
Your skills include C++ programming, Scaled Agile Framework, CI/CD techniques, modern software practices, interoperability, software integration, project and resource management, design controls.
You have skills to build and drive a high-performance teams for results to new product development commitments in software, and have done so in a highly regulated environment, preferred in medical devices.
You have earned a Master's degree in computer science (or equivalent).
You are able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this hybrid position.
Additional Information
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Plymouth, MN.
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.
Learn more about our business.
Discover our rich and exciting history.
Learn more about our purpose.
Read more about our employee benefits.
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.
#LI-PH1
#LI-HYBRID
Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.
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Located in a historic neighborhood in the nation's capital, Georgetown offers rigorous academic programs, a global perspective, exciting ways to take advantage of Washington, D.C., and a commitment to social justice. Our community is a tight knit group of remarkable individuals interested in intellectual inquiry and making a difference in the world.
Requirements
Senior Bioinformatician – Bioinformatics Science – Georgetown University Medical Center
Job Overview
The Senior Bioinformatician supports two main activities – they participate in bioinformatics activities for research projects using genomics data analysis and management - and provide support with courses in Georgetown’s Master's in Health Informatics & Data Science (HIDS).
Due to the rapidly evolving nature of biomedical informatics, they are expected to stay up to date on bioinformatics tools and electronic data capture technologies for different projects.
And toward conducting research coordination and management activities effectively, they assist the development of research plans, the maintenance of research documents, and the tracking of progress on different tasks for various research projects.
Work Interactions and Work Mode Designation
The Senior Bioinformatician works with the research and education leaders of Georgetown Innovation Center for Biomedical Informatics (ICBI) to provide biomedical data analysis support, perform project related literature and database research, develop project plans, and maintain research documents. They also assist in managing the Master’s HIDS program.
Their work positively impacts ICBI’s mission to drive the Medical Center’s innovation and translational biomedical informatics research; and ensures a strong presence for ICBI in the big data in biomedicine space and is essential for grant application submissions to conduct funded research.
As well, they interact with multiple investigators, data managers, research staff and leaders at ICBI and GUMC on a daily basis.
This position has been designated as On-Campus. Please note that work mode designations are regularly reviewed in order to meet the evolving needs of the University. Such review may necessitate a change to a position’s mode of work designation. Complete details about Georgetown University’s mode of work designations for staff positions can be found on the Department of Human Resources website: https://hr.georgetown.edu/mode-of-work-designation.
Requirements and Qualifications
No additional licenses or certificates are required.
Current Georgetown Employees:
If you currently work at Georgetown University, please exit this website and login to GMS (gms.georgetown.edu) using your Net ID and password. Then select the Career worklet on your GMS Home dashboard to view Jobs at Georgetown.
Submission Guidelines:
Please note that in order to be considered an applicant for any position at Georgetown University you must submit a resume for each position of interest for which you believe you are qualified. Documents are not kept on file for future positions.
Need Assistance:
If you are a qualified individual with a disability and need a reasonable accommodation for any part of the application and hiring process, please click here for more information, or contact the Office of Institutional Diversity, Equity, and Affirmative Action (IDEAA) at 202-687-4798 or ideaa@georgetown.edu.
Need some assistance with the application process? Please call 202-687-2500. For more information about the suite of benefits, professional development and community involvement opportunities that make up Georgetown's commitment to its employees, please visit the Georgetown Works website.
EEO Statement:
Georgetown University is an Equal Opportunity/Affirmative Action Employer fully dedicated to achieving a diverse faculty and staff. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to race, color, religion, national origin, age, sex (including pregnancy, gender identity and expression, and sexual orientation), disability status, protected veteran status, or any other characteristic protected by law.
Benefits:
Georgetown University offers a comprehensive and competitive benefit package that includes medical, dental, vision, disability and life insurance, retirement savings, tuition assistance, work-life balance benefits, employee discounts and an array of voluntary insurance options. You can learn more about benefits and eligibility on the Department of Human Resources website.
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INVENT. IMPMROVE. INSPIRE.
NxStage Medical, a Fresenius company is not your typical medical products company. We are a close-knit team of talented professionals driven by a shared commitment: to lead a movement to dramatically improve renal care with innovative yet simple therapeutic solutions that benefit patients, caregivers, and society. We pursue this goal through a passionate commitment to Innovate, Educate, and Advocate for the breakthroughs that are redefining renal care. Additionally, NxStage works in community with its customers, patients, industry partners, and government leaders and agencies to realize the vision of better, simpler, more accessible renal care.
Position Summary:
The Co-ops support product or process development activities related to the development, design, research and manufacturing of NxStage Medical's new and existing suit of products. As part of the R&D team, this involves participating in testing, design, building samples, and other activities as needed by the project team. Co-ops in this position will have the opportunity to work more independently and take on additional responsibilities with their teams. Co-ops may be part of the system engineering, hardware mechanical engineering, or disposables engineering team.
Core Responsibilities:
• Participate in design or development of new medical equipment or disposables and/or upgrades to existing products
• Assist with major projects, or phases of projects, to resolve advanced and complex technical problems
• Ensure all design activities conform to design controls; and that all analysis, design and testing activities are properly documented
• Participate in activities to ensure design and process shortcomings are identified and appropriately addressed
• Assist the product development team in the adoption and use of best practices and design methodologies
• Debug and develop reliability improvements for existing products and products under development.
• Provide technical support for product engineering, design development, integration, test and evaluation
• Investigate the feasibility of new projects, systems or approaches
• Learn about and work in ways that are compliant with internal and external standards, good manufacturing practices, and quality system regulations
Requirements:
• Candidate for BS or MS in Mechanical, Industrial, Plastics, Electrical, or Biomedical Engineering
• Intermediate knowledge of CAD and Technical Drawing creation
• Basic understanding of product and process development of medical devices or similar product experience is desired
• Prior relevant work experience is preferred, such as working in an FDA, defense industry or ISO regulated environment
• Understanding of aspects of system design, electronics, mechanical and software integration or manufacturing processes is beneficial
• Prior experience designing for rapid prototyping as well as traditional manufacturing techniques desired
• Has a constructive approach to teamwork and collaboration
• Demonstrated interest in medical device or pharmaceutical industries
• Excellent technical communication skills and attention to detail, including creating and editing technical procedures, protocols, and reports
• Commitment to performing all tasks with quality and integrity
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
Official account of Jobstore.
INVENT. IMPMROVE. INSPIRE.
NxStage Medical, a Fresenius company is not your typical medical products company. We are a close-knit team of talented professionals driven by a shared commitment: to lead a movement to dramatically improve renal care with innovative yet simple therapeutic solutions that benefit patients, caregivers, and society. We pursue this goal through a passionate commitment to Innovate, Educate, and Advocate for the breakthroughs that are redefining renal care. Additionally, NxStage works in community with its customers, patients, industry partners, and government leaders and agencies to realize the vision of better, simpler, more accessible renal care.
Position Summary:
The Co-ops support product or process development activities related to the development, design, research and manufacturing of NxStage Medical's new and existing suit of products. As part of the R&D team, this involves participating in testing, design, building samples, and other activities as needed by the project team. Co-ops in this position will have the opportunity to work more independently and take on additional responsibilities with their teams. Co-ops may be part of the system engineering, hardware mechanical engineering, or disposables engineering team.
Core Responsibilities:
• Participate in design or development of new medical equipment or disposables and/or upgrades to existing products
• Assist with major projects, or phases of projects, to resolve advanced and complex technical problems
• Ensure all design activities conform to design controls; and that all analysis, design and testing activities are properly documented
• Participate in activities to ensure design and process shortcomings are identified and appropriately addressed
• Assist the product development team in the adoption and use of best practices and design methodologies
• Debug and develop reliability improvements for existing products and products under development.
• Provide technical support for product engineering, design development, integration, test and evaluation
• Investigate the feasibility of new projects, systems or approaches
• Learn about and work in ways that are compliant with internal and external standards, good manufacturing practices, and quality system regulations
Requirements:
• Candidate for BS or MS in Mechanical, Industrial, Plastics, Electrical, or Biomedical Engineering
• Intermediate knowledge of CAD and Technical Drawing creation
• Basic understanding of product and process development of medical devices or similar product experience is desired
• Prior relevant work experience is preferred, such as working in an FDA, defense industry or ISO regulated environment
• Understanding of aspects of system design, electronics, mechanical and software integration or manufacturing processes is beneficial
• Prior experience designing for rapid prototyping as well as traditional manufacturing techniques desired
• Has a constructive approach to teamwork and collaboration
• Demonstrated interest in medical device or pharmaceutical industries
• Excellent technical communication skills and attention to detail, including creating and editing technical procedures, protocols, and reports
• Commitment to performing all tasks with quality and integrity
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
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PURPOSE AND SCOPE:
As co-op with NxStage, a Fresenius Medical Care company, a student will apply classroom based knowledge to workplace experience and will benefit from learning experiences in their major area of study. The co-op supports product or process development activities related to the development, design, research and manufacturing of NxStage Medical's new and existing products. As part of the R&D team, this involves participating in testing, design, building samples, and other activities as needed by the project team. Co-ops may be part of the system engineering, hardware mechanical engineering, or disposables engineering team.
PRINCIPAL RESPONSIBILITIES AND DUTIES:
Participate in design or development of new medical equipment and/or upgrades to existing products
Assist with major projects, or phases of projects, to resolve advanced and complex technical problems
Ensure all design activities conform to design controls; and that all analysis, design and testing activities are properly documented
Participate in activities to ensure design and process shortcomings are identified and appropriately addressed
Assist the product development team in the adoption and use of best practices and design methodologies
Debug and develop reliability improvements for existing products and products under development
Provide technical support for product engineering, design development, integration, test and evaluation
Investigate the feasibility of new projects, systems or approaches.
Learn about and work in ways that are compliant with internal and external standards, good manufacturing practices, and quality system regulations
PHYSICAL DEMANDS AND WORKING CONDITIONS:
The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION:
EXPERIENCE AND REQUIRED SKILLS:
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
Official account of Jobstore.
INVENT. IMPMROVE. INSPIRE.
NxStage Medical, a Fresenius company is not your typical medical products company. We are a close-knit team of talented professionals driven by a shared commitment: to lead a movement to dramatically improve renal care with innovative yet simple therapeutic solutions that benefit patients, caregivers, and society. We pursue this goal through a passionate commitment to Innovate, Educate, and Advocate for the breakthroughs that are redefining renal care. Additionally, NxStage works in community with its customers, patients, industry partners, and government leaders and agencies to realize the vision of better, simpler, more accessible renal care.
Position Summary:
The Co-ops support product or process development activities related to the development, design, research and manufacturing of NxStage Medical's new and existing suit of products. As part of the R&D team, this involves participating in testing, design, building samples, and other activities as needed by the project team. Co-ops in this position will have the opportunity to work more independently and take on additional responsibilities with their teams. Co-ops may be part of the system engineering, hardware mechanical engineering, or disposables engineering team.
Core Responsibilities:
• Participate in design or development of new medical equipment or disposables and/or upgrades to existing products
• Assist with major projects, or phases of projects, to resolve advanced and complex technical problems
• Ensure all design activities conform to design controls; and that all analysis, design and testing activities are properly documented
• Participate in activities to ensure design and process shortcomings are identified and appropriately addressed
• Assist the product development team in the adoption and use of best practices and design methodologies
• Debug and develop reliability improvements for existing products and products under development.
• Provide technical support for product engineering, design development, integration, test and evaluation
• Investigate the feasibility of new projects, systems or approaches
• Learn about and work in ways that are compliant with internal and external standards, good manufacturing practices, and quality system regulations
Requirements:
• Candidate for BS or MS in Mechanical, Industrial, Plastics, Electrical, or Biomedical Engineering
• Intermediate knowledge of CAD and Technical Drawing creation
• Basic understanding of product and process development of medical devices or similar product experience is desired
• Prior relevant work experience is preferred, such as working in an FDA, defense industry or ISO regulated environment
• Understanding of aspects of system design, electronics, mechanical and software integration or manufacturing processes is beneficial
• Prior experience designing for rapid prototyping as well as traditional manufacturing techniques desired
• Has a constructive approach to teamwork and collaboration
• Demonstrated interest in medical device or pharmaceutical industries
• Excellent technical communication skills and attention to detail, including creating and editing technical procedures, protocols, and reports
• Commitment to performing all tasks with quality and integrity
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
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Job Title
Sr. Electrical Engineer R&D
Working at Abbott
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:
The Opportunity
This position works out of our Westford, MA location in the AVD division.
Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease.
This position will be a R&D/Sustaining engineering position supporting the FFR and OCT hardware portion of our business. Performs the layout, construction, and evaluation of a variety of prototype Printed Circuit Boards, fixtures, and tools. Applies engineering and scientific principles to the evaluation and solution of technical problems. Exercises technical judgment in planning, organizing, performing, coordinating and/or directing engineering work. Performs engineering studies. Remains abreast of and consults on technical advancements. Identifies and routinely uses the most effective and cost-efficient practices to execute processes; continually evaluates their effectiveness and appropriateness.
What You’ll Work On
• Support R&D and sustaining activities around OCT and FFR manufacturing including end of life, supplier change requests, Global compliance standards, IFU/Label changes, support of regulatory submissions, corporate programs, literature review, and all supporting quality system elements
• Conduct evaluations, tests, and analyses related to feasibility and function
• The position will also support the following design and manufacturing elements:
• Production support
• Interface with vendors for components
• Protocol and report writing
• Generate and modify material specification documentation
• Work with cross functional teams
• Develop and implement design improvements
• Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
• 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.
Required Qualifications
• Bachelor of Science in electrical/electronic engineering or related engineering field.
• Minimum 9 years of experience or an equivalent combination of education and work experience.
• Relevant work experience in performing the layout construction, and evaluation of a variety of Printed Circuit Boards, knowledge of analog electronics, experience with fiber optics, or capital equipment experience is preferred.
• Ability to understand and comply with applicable FDA regulations and Company operating procedures, processes, policies and tasks preferred.
• Demonstrated personal computer skills, including spreadsheet, word processing, database management, and specialized applications.
Preferred Qualifications
• Medical Devices
• Altium
• Advanced credential or professional certification in a relevant discipline/concentration desired.
• Six-Sigma knowledge and experience desired.
• Training and experience in manufacturing processes and methods desired, especially in the manufacturing of medical devices preferred.
• Ability to work in a highly matrixed and geographically diverse business environment.
• Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
• Ability to leverage and/or engage others to accomplish projects.
• Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
• Multitasks, prioritizes and meets deadlines in timely manner.
• Strong organizational and follow-up skills, as well as attention to detail.
• Ability to travel approximately 25%, including internationally.
• Ability to maintain regular and predictable attendance.
* 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.
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.
The base pay for this position is
$95,000.00 – $190,000.00In specific locations, the pay range may vary from the range posted.
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
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Responsibilities:
Requirements:
Interested candidates can forward their CVs in MS Word format to alex@triton-ai.com
Reg No. R1549345
Triton AI Pte Ltd
License no. 21C0661
Official account of Jobstore.
INVENT. IMPMROVE. INSPIRE.
NxStage Medical, a Fresenius company is not your typical medical products company. We are a close-knit team of talented professionals driven by a shared commitment: to lead a movement to dramatically improve renal care with innovative yet simple therapeutic solutions that benefit patients, caregivers, and society. We pursue this goal through a passionate commitment to Innovate, Educate, and Advocate for the breakthroughs that are redefining renal care. Additionally, NxStage works in community with its customers, patients, industry partners, and government leaders and agencies to realize the vision of better, simpler, more accessible renal care.
Position Summary:
The Co-ops support product or process development activities related to the development, design, research and manufacturing of NxStage Medical's new and existing suit of products. As part of the R&D team, this involves participating in testing, design, building samples, and other activities as needed by the project team. Co-ops in this position will have the opportunity to work more independently and take on additional responsibilities with their teams. Co-ops may be part of the system engineering, hardware mechanical engineering, or disposables engineering team.
Core Responsibilities:
• Participate in design or development of new medical equipment or disposables and/or upgrades to existing products
• Assist with major projects, or phases of projects, to resolve advanced and complex technical problems
• Ensure all design activities conform to design controls; and that all analysis, design and testing activities are properly documented
• Participate in activities to ensure design and process shortcomings are identified and appropriately addressed
• Assist the product development team in the adoption and use of best practices and design methodologies
• Debug and develop reliability improvements for existing products and products under development.
• Provide technical support for product engineering, design development, integration, test and evaluation
• Investigate the feasibility of new projects, systems or approaches
• Learn about and work in ways that are compliant with internal and external standards, good manufacturing practices, and quality system regulations
Requirements:
• Candidate for BS or MS in Mechanical, Industrial, Plastics, Electrical, or Biomedical Engineering
• Intermediate knowledge of CAD and Technical Drawing creation
• Basic understanding of product and process development of medical devices or similar product experience is desired
• Prior relevant work experience is preferred, such as working in an FDA, defense industry or ISO regulated environment
• Understanding of aspects of system design, electronics, mechanical and software integration or manufacturing processes is beneficial
• Prior experience designing for rapid prototyping as well as traditional manufacturing techniques desired
• Has a constructive approach to teamwork and collaboration
• Demonstrated interest in medical device or pharmaceutical industries
• Excellent technical communication skills and attention to detail, including creating and editing technical procedures, protocols, and reports
• Commitment to performing all tasks with quality and integrity
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
Official account of Jobstore.
INVENT. IMPROVE. INSPIRE.
NxStage Medical is not your typical medical products company. We are a close-knit team of talented professionals driven by a shared commitment: to lead a movement to dramatically improve renal care with innovative yet simple therapeutic solutions that benefit patients, caregivers, and society. We pursue this goal through a passionate commitment to Innovate, Educate and Advocate for the breakthroughs that are redefining renal care. Additionally, NxStage works in community with its customers, patients, industry partners, and government leaders and agencies to realize the vision of better, simpler, more accessible renal care.
Position Summary:
The co-op supports product or process development activities related to the development, design, research and manufacturing of NxStage Medical's new and existing products. As part of the R&D team, this involves participating in research, testing, documenting activities, building samples, and other activities as needed by the project team. Co-ops will support the Human Factors and Usability engineering team.
Core Responsibilities:
Requirements:
EXPERIENCE AND REQUIRED SKILLS:
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity
Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.
Official account of Jobstore.
