We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further - Haemonetics is your employer of choice.
Translates customer needs into software technical requirements supporting product research, design, life cycle management, and/or product and systems development/ integration. This position applies knowledge of multiple specialized and/or interdisciplinary technical areas, project management, and systems design and integration needs.
Using current programming language and technologies, creates software components and applications to support medical device product development. Analyzes, designs, documents, programs, and debugs software programs; modifies software enhancements of existing computer programs which control the real time operation of the medical device using embedded software applications. May be responsible for the development of device drivers, application control, or user interfaces, and may design and develop algorithms for device diagnostics, communications, interactive and automated applications and/or test programs.
Analyzes experimental data, develops technical conclusions, and evaluates potential applicability of recommendations. Sets technical priorities for complex matters, when difficult compromises must be made (i.e. acts with or guides others toward the proper balance of effort vs. timeliness, and technical improvements and innovation with practical business constraints).
Coordinates work primarily across project team(s), related groups, or within the department. Communicates proactively and effectively at all levels. Expands understanding and employs sensitivity in communications with culturally diverse audiences.
Researches issues outside technical capability and selects most efficient methods/techniques to achieve objectives. Applies appropriate standards, processes, policies, procedures, practices and tools throughout the product/system development lifecycle, including Standard Operating Procedures (SOP's), and applicable medical device development protocols under FDA Quality Systems Regulations, CE Marking, and ISO Quality Systems.
Independently solves a wide range of complex and diverse problems and evaluates short term impact of recommendations.
Participate design reviews at the sub-system level.
Learns basic Patent policies, procedures, and business issues and becomes familiar with the competitive "Patent Landscape" as related to assigned work.
May assist with systems architecture development at the sub-system level. Works on high impact assignments where speed, quality, and efficiency significantly impacts results.
Ideal Candidate has experience with:
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