Technical Writer – Kelly Engineering, Project Services
Largo, Florida.

Client in medical devices is seeking a detail-oriented Technical Writer to support biocompatibility compliance efforts driven by evolving EU MDR (European Union Medical Device Regulation) requirements. This contract role will focus on updating and documenting manufacturing process flows for approximately 130 technical files and nearly 500 catalog numbers related to our sports medicine disposable orthopedic devices.

Key Responsibilities:
Review existing manufacturing documentation and collaborate with the engineering team.
Identify and document all processes and materials used in the manufacturing of finished goods and subassemblies.
Create detailed, end-to-end manufacturing process flow maps to support technical file updates and biocompatibility needs.
Maintain a high level of accuracy and organization in updating technical documents as required for EU MDR compliance.

Projec...