Technical Writer Job at Extremity Care in Conshohocken

Purpose

The Technical Writer is responsible for the creation of technical documentation for various types of products, services, and processes.

Responsibilities

• Create, write, outline, and edit technical documents to include standardized operating procedures, work instructions, process flows, technical specifications, reference manuals, and product manuals.
• Perform and document change order routing approvals in the electronic quality management system.
• Work with subject matter experts and internal teams to obtain in-depth understanding of the subject/process to ensure accurate development of process, product, and technical documentation requirements.
• Edit and format documents to be clear, concise, and easy to read in a way that is visually appealing and easy to navigate.
• Draft, create, and maintain document templates based on process need.
• Manage documentation projects, including planning, scheduling, and coordinating with other teams and stakeholders.
• Support internal and external audits.
• Maintain a working knowledge of relevant FDA CFRs, AATB standards, internal policies and standard operating procedures.
• Maintain acceptable attendance and punctuality for scheduled work hours and meetings.
• Ensure completion of assigned tasks and responsibilities within defined timeframes.
• Maintain flexibility to work outside of normal business hours during weekdays or weekends with reasonable advance notice to support business/operational needs when necessary.
• Perform other duties as assigned.

Skills

• Ability to work independently and in a team environment
• Excellent attention to detail and organization
• Excellent written and verbal communication
• Highest level of ethics and integrity
• Ability to lead and motivate the right behaviors
• Ability to multi-task and work in a fast-paced environment
• Strong technical writing
• Effective project management
• Proficiency in Microsoft Office

Qualifications/Requirements

• Bachelors degree in English, technical writing, or related field required.
• At least 2 years of technical writing and/or document control experience required.
• At least 1 year of experience in an FDA regulated industry for quality preferred.
• Clearance of favorable background investigation required.