Technical Writer

Technical Writer

Summary:

• The Technical Writer will assist with document management system administration at the Sanford, NC site. The role manages document workflows within the Pfizer global electronic document management system and provides administrative approval for document promotions. In addition, this individual provides guidance to document authors on document workflows and provides input on document standards and requirements.

Responsibilities:

• Technical Writing role revises/reformats Standard Operating Procedures (SOPs), training materials, and other related documents in accordance with current approved site templates and subject matter expert requests.
• Manages documents through various workflows, ensures document properties are appropriately set, and provides administrative approval for document promotion.
• Follows the necessary change management processes to maintain compliance during creation of new and revision of existing documents. Review the impact of proposed changes with regards to other support documents.
• Assures new and revised site documentation/procedures are:
• Current and consistent with related/similar documents.
• Meet internal control policies and regulations.

Qualifications:

• Minimum High School Diploma with a minimum of 3 years experience documentation-related or supporting function is required, preferably in a Biopharmaceutical or other regulated environment OR Bachelor's degree with 1 - 2 years' of experience in documentation-related or supporting function is required, preferably in a Biopharmaceutical or other regulated environment.
• Able to quickly learn and navigate electronic systems to facilitate routine operation and maintenance of the site documentation system and related processes.
• Able to write clearly and concisely with excellent grammar, good writing skills and communication.
• Skilled in word processing and document formatting; experienced in Microsoft Office applications (Word, Excel, PowerPoint, Visio).
• Able to effectively proofread documents prepared by self and others for content and others to ensure content and formatting accuracy.
• Demonstrates an ability to adapt to shifting priorities, change, stress and to find appropriate balance between needs of the organization, others and self. Incorporates insights of other people into ongoing work.
• Understanding of cGMP and Safety regulations.
• Strong organizational and communication skills.
• Team based collaborative problem solving.

Rate:

• $30 - $33 per hour
• This role will be onsite in Sanford, NC

Please note contractors are engaged to provide services to Pfizer on a temporary basis in connection with a specific assignment. Contractors are hired and employed through Atrium, our third-party payrolling partner.

This job posting is for a temporary role as an employee of Atrium on assignment at Pfizer. The individual selected for this role will be offered the role as an employee of Atrium; compensation, medical benefits, fringe benefits, and other terms and conditions of employment shall be presented by Atrium upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued, and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.

Salary : $30 - $33