Employment
We are always looking for outstanding additions to our staff. We would be interested in hearing from prospective employees with the following areas of experience and interest. All openings currently under consideration are for our Boston and Chicago area facilities. Some travel may be required.
Current Openings
Software Developers - Intertech Engineering works with a wide range of technologies and applications almost exclusively related to medical device development. Experience with C, C++, and C#, Visual Basic, custom kernels, various commercial RTOS packages (e.g. Nucleus, PharLap ETS, VxWorks and ThreadX), Windows, Windows CE, .NET, Linux, OpenGL, SQLServer all are of interest to us. Intertech is an outsource engineering provider to the medical device industry focusing on software and electronics technologies, along with the QA, compliance, and project management expertise that is required in the FDA regulated industry. Projects are fast paced with constant project turnover that keeps the work interesting. We are looking for experienced software developers to join our team. Projects are organized by teams that operate primarily from our offices in Westwood, MA and Lincolnshire, IL. Some travel may be required occasionally. A diverse background, ability to work in a structured regulatory environment, and a willingness to do whatever it takes to get the job done are the keys to success.
Principal Software Engineers - Illinois and Massachusetts Offices 10+ years of experience in relevant languages and operating environments. Medical device experience not required, but preferred. In addition to strong software development skills, programming skills, and a mastery of the attributes required of our Senior Software Engineers, successful candidates for Principal Software Engineering positions will have the following attributes:
- Ability to act as a technical lead on larger projects, and as project manager on smaller projects.
- Ability to discuss and review with client the engineering processes required by the project.
- Ability to manage a positive relationship with client and demonstrate a mastery of technical area to client.
- Ability to evaluate defect trends and process flaws.
- Ability to analyze customer requirements and select approach and tools required.
- Ability to identify new project tasks and estimate durations for completion for overall software projects.
- Evaluate and identify trends and suggest directions to expand Intertech’s abilities.
- Ability to assist in proposal discussions, and preparation.
- Ability to motivate and encourage subordinates and peers.
- Ability to work on and manage subordinates on several projects.
- S
et up schedule and/or means of communication for project team to remain informed throughout project
Submit Resume - Please indicate position for which you are applying. Include salary requirements.
Senior Software Engineers - Illinois and Massachusetts Offices
5+ years of experience in relevant languages and operating environments. Medical device experience not required, but preferred. In addition to strong software development and programming skills, successful candidates will have the following attributes:
Submit Resume - Please indicate position for which you are applying and include salary requirements.
Future Openings Although we do not have an immediate opening for the following positions, we do anticipate openings in the near future. Send a resume for our active file if you think you are a good fit.
Quality Specialists - We are specifically interested in software quality professionals, specifically those with medical device industry experience. Experience with SOP development, internal/external auditing, review techniques, software test planning, design, and procedure development, or any other aspect of software validation are good backgrounds for positions at Intertech. Writing skills and a mastery of English are a must. Some positions may require some speaking and training skills. Submit Resume - Please indicate position for which you are applying
Regulatory Specialists - Our expansion of services has created a need for an FDA regulatory specialist. Our ideal candidate will be experienced in writing and managing regulatory submissions for a number of different types of products. Managerial skills in working with developers to execute a regulatory strategy are desired. Ability to deal with regulatory agencies on behalf of our clients is also desired. Independent regulatory consultants wanting a more stable work environment would be a good fit. Writing skills and a mastery of English are a must. Some positions may require some speaking and training skills. Submit Resume - Please indicate position for which you are applying
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