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 Norwood, MA facility. Some travel may be required. Prospective employees should send a resume and note detailing specific position of interest to us at resumes@intertechengineering.com.

Developers - We are interested in developers with medical device experience, or experience in another industry in which software development is regulated. We also are interested in developers without specific industry experience but who are interested in and dedicated to software development that adheres to a well defined process.

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.

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.