Location: St. Paul, MN Duration: 12 months Position Responsibilities Prepares robust regulatory applications or technical file documentation to achieve departmental and organizational objectives and support EU MDR transition activities. Creates, reviews and approves engineering change orders. May act or assist as a regulatory representative on core product development teams, communicates regulatory requirements and impact of [...]
Location: Mounds View, MN Duration: 12 months (potential contract to hire) Position Description This position is responsible for planning, research, and technical writing support for medical device industry product labeling within CVG Technical Communication. Position Responsibilities Seasoned technical writing professional who provides labeling support to product development teams, including: Able to translate complex product information [...]
Location: Plymouth, MN Duration: 6+ months Position Description Seeking a technical writer who has experience with quality documentation in a medical device and validation environment. The candidates should have experience with at least two of following deliverables: user user-requirement specifications (URS), functional specs. (FS), install verification (IV), operation test protocols (OTP). Min. of 3-5 years’ [...]