PRINCIPAL ACCOUNTABILITY
Under the direction of the Manager of Procedure Development, the Technical Writer 1’s role is to develop written information to enable the end user to perform regulated job tasks in accordance with regulatory, manufacturer, and company guidelines.
Technical Writing staff is responsible for research, development, and maintenance of Carter BloodCare (CBC) Standard Operating Procedures (SOPs), (SOPs, forms, labels, validations, studies and memos). SOP’s are written and maintained in accordance with regulatory standards including, but not limited to, FDA, AABB, OSHA, manufacturer recommendations, and CBC guidelines in the Quality Standard Manual.
The position must exhibit excellent written, verbal, and collaboration skills. They must have the ability to interpret technical information for technical and non-technical personnel use. This position liaise with department subject matter experts, end-users, manufacturers, quality assurance and process improvement staff, medical directors, department management, and external vendors.
Regular full-time attendance is required during office hours.