MedTech maintains this listing of available jobs at member companies as a service to its members and to the region's medical technology industry. We hope this service is helpful both to medical technologies organizations seeking qualified employees and to those individuals looking to begin or change careers in the medical technologies industry. MedTech members may post positions and/or provide a hyperlink to their own online Job Board; please direct all inquiries about Job Bank listings to the listed contacts. Please send job posting submitions to careers@medtech.org
AngioDynamics, Inc.
Research Engineer – 2 positions available (Fremont, CA) – posted 4/17/08
AngioDynamics was founded in Queensbury, NY in 1988 and has grown into a NASDAQ-listed public company with a total market capitalization of more than $300 million. Over the past 20 years, the Company has distinguished itself as a dynamic brand in a technologically competitive, high-growth industry. This position will be responsible for the design and development of new products from the initial concept stage through demonstration of feasibility. Development of the basic science will involve predictive modeling, prototype design and fabrication as well as the development and execution of tests (bench and animal) to verify the theoretical predictions. Ideal candidates will possess at least 7 years experience in medical device environment, experience in interventional oncology a plus, and a Bachelor’s degree in Mechanical, Electrical, or Biomedical Engineering. Proficiency in Solid Works is preferred. Candidates wanting to work in a fast growing, innovative company, should forward resumes and salary requirements to: Human Resources Department, AngioDynamics, Inc., hr@angiodynamics.com.
AngioDynamics, Inc.
Product Development – Product Manager (Queensbury, NY) – posted 4/17/08
AngioDynamics was founded in Queensbury, NY in 1988 and has grown into a NASDAQ-listed public company with a total market capitalization of more than $300 million. Over the past 20 years, the Company has distinguished itself as a dynamic brand in a technologically competitive, high-growth industry. This position will be responsible for managing the development of new projects through the Design Control system to commercialization. This will include developing, maintaining and monitoring project budgets, directing the use of resources to effectively complete projects, recruit and supervise product development technical staff, interface with marketing, regulatory and quality assurance, and continually improve upon the time-to-market cycles for new product designs. Ideal Candidates will possess a 4 Year Engineering Degree in Biomedical or Mechanical Engineering, at Least 3 years prior experience as a Project Engineer, at Least 10 years prior experience in the development of medical devices, and proven experience as a successful team leader. Candidates wanting to work in a fast growing, innovative company, should forward resumes and salary requirements to: Human Resources Department, AngioDynamics, Inc., hr@angiodynamics.com.
AngioDynamics, Inc.
Product Development Engineer – 5 positions available (Queensbury, NY) – posted 4/17/08
AngioDynamics was founded in Queensbury, NY in 1988 and has grown into a NASDAQ-listed public company with a total market capitalization of more than $300 million. Over the past 20 years, the Company has distinguished itself as a dynamic brand in a technologically competitive, high-growth industry. This position will be responsible for designing and developing new products from initial concept stage through to production. The position entails developing and testing the feasibility of new product concepts, translating concepts into design prototypes, assisting in project budgeting, and interfacing with marketing, regulatory and quality assurance departments. Ideal Candidates will possess a 4 Year Engineering Degree, at Least 5 years prior experience in the medical device engineering field, and proven experience with team approach to product development. Experience with SolidWorks and Statgraphics is a plus. Candidates wanting to work in a fast growing, innovative company, should forward resumes and salary requirements to: Human Resources Department, AngioDynamics, Inc., hr@angiodynamics.com.
AngioDynamics, Inc.
Quality Engineer – new position (Queensbury, NY) – posted 4/17/08
AngioDynamics was founded in Queensbury, NY in 1988 and has grown into a NASDAQ-listed public company with a total market capitalization of more than $300 million. Over the past 20 years, the Company has distinguished itself as a dynamic brand in a technologically competitive, high-growth industry. This position will be responsible for assuring product quality through participation in cross-functional product development teams and by supporting manufacturing operations. This role will provide QE support for existing products and assist with the transfer of new products to production to drive continual improvement, utilizing quality tools to implementing quality improvements, process mapping, process validations, software validations, production efficiency improvements, and process controls. Ideal Candidates will possess a Bachelor of Science degree in the allied health science area (or equivalent experience), three (3) to five (5) years experience in the FDA-regulated industries (or equivalent combination of education, training, and experience), proven ability to use MS Word, Excel, and databases, Statistical Process Control and knowledge of statistical analysis techniques, Validation/Qualification/Verification protocol development, excellent organizational skills, good verbal and written communication skills, and an in-depth knowledge of FDA cGMP/QSR’s and ISO 13485 standards. Software validation/verification and supervisor experience is preferred. Certified Quality Engineer (CQE) is desirable. Candidates wanting to work in a fast growing, innovative company, should forward resumes and salary requirements to: Human Resources Department, AngioDynamics, Inc., hr@angiodynamics.com.
AngioDynamics, Inc.
Marketing Product Manager – 3 new positions (Queensbury, NY) – posted 4/17/08
AngioDynamics was founded in Queensbury, NY in 1988 and has grown into a NASDAQ-listed public company with a total market capitalization of more than $300 million. Over the past 20 years, the Company has distinguished itself as a dynamic brand in a technologically competitive, high-growth industry. This position will be responsible for developing markets by identifying potential products, working out specifications and timetables with Product Development, initiating test markets, and developing marketing and pricing strategies. This will include determining customers’ needs and desires and product pricing by specifying the research needed to obtain market information; recommending the nature and scope of present product lines by appraising new product ideas and/or product or packaging change; and assessing market competition by comparing the company’s product to competitor’s products. Ideal Candidates will possess 3-4 years marketing/sales experience in medical related fields, particular experience with Focal Cancer Therapy, Surgical Devices or Venous Disease, and a Bachelor’s degree in Business/Marketing/or related field. An MBA is Preferred. Candidates wanting to work in a fast growing, innovative company, should forward resumes and salary requirements to: Human Resources Department, AngioDynamics, Inc., hr@angiodynamics.com.
AngioDynamics, Inc.
Clinical Events Manager – new position (Queensbury, NY) – posted 4/17/08
AngioDynamics was founded in Queensbury, NY in 1988 and has grown into a NASDAQ-listed public company with a total market capitalization of more than $300 million. Over the past 20 years, the Company has distinguished itself as a dynamic brand in a technologically competitive, high-growth industry. This position will be responsible for planning and managing clinical events, including symposia and trade-shows for AngioDynamics. This role will work to develop a strategic plan for clinical events while working with the marketing staff on execution of each event and working with the Mar Comm Director and product management team to develop messages, graphics and promotional materials. Ideal Candidates will possess 5+ years experience in marketing events management, well-developed project management skills, Proficiency in Microsoft Office (Word, Excel), excellent verbal and written communication skills, self-starter who is able to work well within the group environment, and an ability to handle multiple priorities in a fast-paced environment. A BA degree in Marketing or equivalent experience is preferred. Candidates wanting to work in a fast growing, innovative company, should forward resumes and salary requirements to Human Resources Department, AngioDynamics, Inc., hr@angiodynamics.com.
Vybion, Inc.
Project Manager Protein Engineering (Ithaca, NY) - posted-7/22/07
Vybion’s novel protein engineering technology platform, ProCode, improves protein solubility, selects and affinity matures monoclonal antibodies and improves biologic function. This platform technology is being applied to biologics and reagent markets. Our collaboration with Cornell University creates an active and challenging environment. Vybion seeks a Senior Scientist capable of leading the commercial implementation of this technology, managing technical and scientific personnel, interacting with clients and implementing project solutions. The position requires a self starter with creative strengths and the ability to motivate others. Requirements include a Ph.D. in a relevant scientific discipline, strong organizational and communication skills, extensive knowledge and experience in molecular biology, ability to translate platform science into effective high throughput system, extensive experience with protein engineering technologies and molecular techniques, team orientation, and an excellent background in protein interactions. Experience with monoclonal antibody selection and affinity maturation technologies and with implementing platform based protein engineering technology in a commercial setting is desired. Please contact with resume to lhenderson@vybion.com or fax to 607-257-6356. Vybion is an equal opportunity employer.
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Laboratory Alliance of Central New York, LLC
Medical Technologists (ASCP), and Medical Laboratory Technicians (Liverpool, NY) Posted-11/30/07
Laboratory Alliance is seeking qualified Medical Technologists (ASCP) and Medical Laboratory Technicians. Responsibilities: Utilizing independent judgement performs both routine and complex laboratory procedures including: diagnostic testing, result reporting, quality control and quality assurance, equipment maintenance, and trouble shooting. Qualifications: Baccalaureate degree in Medical Technology or related field or qualify as a Medical Technologist under New York State Department of Health regulation Part 58-2.4. MT (ASCP) certification preferred. A.A.S. degree in a medical laboratory technician program or related field or qualify as a Medical Laboratory Technician under New York State Department of Health regulation Part 58-2.A. MLT (ASCP) preferred. www.LaboratoryAlliance.com
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Seneca Data
Business Development Engineering Manager (North Syracuse, NY) Posted-11/30/07
Seneca Data is seeking a Business Development Engineering Manager for its North Syracuse Facility. Responsibilities include: managing the development and qualification of components used in product designs for desktops, portables, and server computer platforms. Leading their team to provide engineering management for both internal development programs and ODM development programs, management of component technology roadmaps and driving proactive support to the platform development teams. www.senecadata.com/Careers/careerOpp.aspx
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Deadline Solutions
Automation Programmer (Syracuse , NY)
Deadline Solutions, Inc. is seeking a candidate to fill a mid-level engineering position: PLC and HMI experience a must. Our controls group continues to grow! If you have experience with any of the following platforms, we want to talk to you: AB, GE, ABB, or Delta V. HMI applications associated to those platforms a must. Salary is based on experience. Email resume and cover letter to info@deadlinesolutions.com, www.deadlinesolutions.com
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RTEmd
Medical Software Test Technician (Pittsford, NY) Posted-12/5/07
We are currently looking for an number of individuals that will be involved in planning, executing, and documenting medical software test activities. Individuals should have experience in the verification and validation of medical diagnostic device software. A BA/BS/BT in Laboratory Science, Biomedical Science, or similar is preferred along with 3-5 years of related job experience. Strong experience with FDA QSR requirements and ISO9001-compliant processes is a plus. Experience with BL2 lab procedures is also desired. www.rtemd.com
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RTEmd
Embedded Software Engineer (Pittsford, NY ) Posted-12/5/07
We are currently looking for engineers with embedded software development experience to create a new medical device. Potential candidate must possess good communication skills, be an independent worker and have the ability to meet the demands of a set schedule. Skills should include C/C++; real-time programming of mechanical motion (with timing constraints); RTOS and UNIX operating system (ideally QNX); and modular/component design. Require experience in integrating software and hardware. Duties focus on design, code and test of new features for medical device in an ISO-9000 and FDA compliant development process. Flexibility to travel regionally (within Rochester). www.rtemd.com
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RTEmd
Microsoft Windows Software Engineer (Pittsford, NY) Posted-12/5/07
We are currently looking for senior-level engineers with Visual C/C++ experience. Potential candidate must possess good communication skills, be an independent worker and have the ability to meet the demands of a set schedule and customer quality software processes. Skills should include ability to design, code and test new features as well as troubleshoot existing code. Familiarity with .NET, MFC, ODBC, Visual Studio and Visual SourceSafe a plus. Flexibility to travel regionally. www.rtemd.com
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Conmed Corporation
Senior info System Analyst (Utica, NY) Posted- 12/5/07)
A Senior Information Systems Analyst is needed to manage, develop, coordinate and deploy internally created or externally purchased applications/ projects using previously gained knowledge, staff or outside resources. Other duties include: Create/modify computer applications. Experience developing in Microsoft Visual Studio.net, Visual Basic, ASP.net, C#, IIS, web development, Access and Excel. Manage projects and project teams. Database Administration responsibilities within Oracle and SQL Server. Mentor and train staff in technical areas.
Qualifications: Bachelor's and 3 years' experience
Please apply online at www.conmed.com to view our extensive benefits and learn about the exciting growth our company has experienced.
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Cornell University
Tenure-Track Faculty Position - Biomedical Engineering (Ithaca, NY) Posted- 11/30/07
Cornell anticipates openings for two tenured or tenure-track faculty positions for candidates workings at the interface of engineering and life science who thrive on interdisciplinary research and teaching. Cornell has formed a new Department of Biomedical Engineering (BME) that seeks to bridge medicine, biology, and engineering. Candidates must have a truly outstanding record of excellence in research and education. Research in any area of biomedical engineering will be considered, although we are particularly interested in candidates focused on novel imaging technologies and probe development, applications of micro/nanofabrication in medicine and soft tissue biomechanics. Interested candidates should send a letter of interest, curriculum vitae, brief statement of research and teaching interests, list of recent externally supported research, and names of three references to:https://fastbme.ece.cornall.edu. Qualifications: Candidates should have a PhD in Biomedical Engineering or related technical field. Review of applications will continue until these positions are filled.
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Welch Allyn
Senior Vice President, General Counsel (Skaneateles Falls, NY) Posted-1/21/08
The General Counsel exercises leadership and management responsibility over the legal and public affairs of Welch Allyn and its subsidiaries, including the legal department and outside counsel, serves as secretary to the Board, provides legal guidance to the Board and senior management, assures compliance with regulatory bodies, and protects Welch Allyn from legal and associated risks. Reporting to the President and CEO, initial objectives will relate to assessing Welch Allyn’s legal infrastructure for appropriateness, evaluating effectiveness and efficiency of approach to FDA compliance, and evaluating current intellectual property (IP) patent strategy and practice, recommending changes in all areas as appropriate. As the central contact point for employees, management and Board of Directors, you will advise the Board, CEO and staff on legal / policy issues affecting Welch Allyn business. Serving as corporate secretary for board meetings, you will draft resolutions, minutes and advise on corporate governance issues whenever you deem necessary or when required by the Board You will also review, drafts, approve (and may also negotiate) contracts, as well as create form agreements for recurring matters, and be responsible for Corporate Compliance programs and as collaborator with Internal Audit, you will assure compliance with regulatory bodies. Providing leadership in protecting and leveraging of intellectual property for strategic and commercial advantage, you will coordinate with outside patent counsel on strategy and costs and with outside trademark counsel on portfolio issues. Government affairs and public policy responsibilities will include monitoring proposed legislation and regulations related to manufacturing and the medical device industry. As a member of the senior leadership for the company, you will develop critical path charts. In addition to a J.D./LL.B degree and license / eligibility to practice law in New York, experience as a General Counsel in a health care (FDA regulated) environment, managing legal staff in a growing corporation with revenues over $500 million is required. Hands-on experience with FDA compliance, IP, transactions, government & public affairs and contracts is essential for success. Please contact Jack Boyce.
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InfiMed
Director of Quality Assurance (Liverpool, NY) Posted-1/25/08
Serving as an integral and hands-on member of the senior management team, the Director of Quality Assurance drives the quality efforts for InfiMed and works with the Vice President of Research and Design to lead and expand the strategic expansion of InfiMed’s software development process. The Director of Quality Assurance ensures that all products are manufactured in accordance with the company’s Quality Assurance Program, FDA and international requirements, as well as customer specifications. The director establishes procedures to ensure that the QA program complies with applicable FDA regulations and ISO standards while directing quality related activities with Manufacturing, Engineering, Purchasing and Customer Service. This quality product is designed and shipped by the ultimate authority of the Director of Quality Assurance. For more information or to apply.
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InfiMed
Sr. Medical Imaging Specialist (Liverpool, NY) Posted- 1/25/08
Senior Medical Imaging Specialist conducts leading-edge research in medical image processing for Digital Radiography, Fluoroscopy, Angiography, and Cardiac products for automatic collimator detection, image contrast/sharpness enhancement, image registration, image stitching, 3D reconstruction and other related areas. The Sr. Medical Imaging Specialist interacts with physician sand medical personnel to define and clinically validate requirements to develop algorithms, tools and systems that provide medical image enhancement. In order to aid the development of these products, the Sr. Specialist will initiates technology and knowledge transfers. For more information or to apply.
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Deadline Solutions, Inc.
C++/C# Software Engineer, Senior Level (Syracuse, NY) Posted- 1/28/08
If you are seasoned engineer with high level programming skills, then Deadline Solutions would love to talk to you! We offer exciting opportunities in the manufacturing software industry. Database experience would also be a plus. Salary is based on experience. Email resume and cover letter to hr@dsisyr.com
>http://www.deadlinesolutions.com/
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Deadline Solutions, Inc.
Electrical Engineer (Syracuse, NY) Posted- 1/28/08
Instrumentation, automation & panel design engineering. Our electrical design group is growing. We have exciting opportunities related to panel, equipment and skid design - electrical. Email resume and cover letter to hr@dsisyr.com
>http://www.deadlinesolutions.com/
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Deadline Solutions, Inc.
Automation Design/Test (Syracuse, NY) Posted- 1/28/08
Engineer – Specification/Validation: DCS and Automation Test plan Experience a must. Responsibilities include generating Life Cycle documentation to support system design and requirements traceability for Manufacturing Software systems. Email resume and cover letter to hr@dsisyr.com
>http://www.deadlinesolutions.com/
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Research Dynamics Consulting Group, Ltd
Site Project Manager (Rochester, NY) Posted- 2/1/08
We have an immediate opening in our Rochester office for a Site Manager. A Site Project Manager manages all the investigator sites in a clinical study. The Site Manager would work with the site staff, coordinator and investigator to ensure the site performs well with the protocol. The management includes responsibilities for on-time start up for each site, (ensure IRB approval, and all start up activities completed on time), ensure timely patient enrollment, answer all site protocol questions, and review by internet all case report forms. It does not include any on-premises management of staff or patients. This position requires someone with clinical research experience and a clinical nursing background (RN) to answer the staff' protocol questions. This position requires clinical expertise as you will also review all the clinical data for accuracy and clinical compliance to the protocol. Some management experience is a plus as you are managing the investigator and their staff to ensure performance for our clients. With question or to apply contact Lorraine Ellis or Thomas Hynds.
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Micropen Technologies
Corporate Quality Assurance Manager (Honeoye Falls, NY) Posted- 3/28/08
Micropen Technologies Corporation is a leader in precision dispensing of materials for applications in the biomedical, medical device and electronics markets. This position reports to the Vice-President of Operations with responsibilities for the design, implementation and continuous improvement of all corporate processes and practices. Specific responsibilities include: leading a team chartered to achieve compliance in ISO 13484:2003 standard; management of manufacturing validation processes for specific new products; leadership in workforce capability development; management of corporate documentation overhaul; member of the corporate lean manufacturing team; manage supplier quality program; provide guidance to production staff for all continuous improvement activities. Candidate will have 5+ years in Quality Assurance Management, preferably in the medical device or pharmaceutical manufacturing environment; hands-on experience in ISO 13485:2003 and relevant FDA manufacturing requirements; a demonstrated ability to train, develop and coach employees in compliance processes and practices; and demonstrated team and leadership skills. Please contact Roxanne Panipinto, Manager of Administration, for more information.
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Bristol-Myers Squibb
Executive Assistant (Syracuse, NY) Posted- 4/9/08
Position supports VP Syracuse Biologics and his leadership team. Performs highly diverse administrative duties which by nature of the position involves high level contacts and exposure to sensitive information, which necessitates great skill in the areas of tact, diplomacy, discretion, judgment, and confidentiality. Responsibilities include but are not limited to creating project management and follow up systems to support the VP in his daily duties, handling correspondence, proactively managing calendars, scheduling meetings and conferences, making travel arrangements, preparing expense reports, and maintaining records and files. Utilize time management techniques to effectively manage priorities and assist the VP in managing his activities. The position requires a highly experienced professional with experience working for a senior level executive with a high school diploma and associates degree preferred. In addition, he or she must have a minimum of 5 years relative experience. Must be well organized and have excellent verbal and written communication skills. Candidate must be comfortable working in a fast passed environment, sometimes working with short deadlines. Demonstrated experience in project and task management. Must be proficient in various computer applications including MS Word, Power Point, Excel, email, electronic calendar, web based travel arrangements, and expense reporting systems. Must be familiar with all BMS systems and software and easily adaptable to new learning situations. Knows how to set priorities and work with little supervision. Please apply online at www.bms.com.