Technical Writer

Date:

May 31, 2008

Location:

2 Fourth Avenue

Burlington, Ma. 01803

Job description:

The position will report to the vice president of engineering. The successful Technical Writer will be responsible for creating a variety of technical documentation to support a QSR and ISO 13485 compliant medical device design and manufacturing environment . The documentation will include product design specifications, , software requirements documentation, software validation protocols and reports, process validation protocols and reports, and Standard Operating Procedures. The individual will also be responsible for additional of writing responsibilities as needs arise.

The individual must communicate well and be willing to collaborate with a variety of disciplines on project teams and with individual contributors in the organization. They also must be proficient in MS office programs. Knowledge in CAD/CAM software would be an added plus.

Required
A minimum of 4 years experience in Technical or Scientific writing
A minimum of 6 years experience in Microsoft Office desktop publication tools

Preferred
Bachelor's Degree in a technical or scientific field

Medical device experience

Experience in software documentation

Travel required:

Minimal

Telecommute:

no

The Compensation and Benefits:

This position offers a competitive compensation package; including 80% company- paid medical, dental, vision, life and disability insurances.  Stock options and a 401(k) plan are also offered.

ConforMIS is an EEO Employer

 Interested candidates should contact john.slamin@conformis.com