About this opportunity
Planet Pharma lists this Technical Writer opportunity in clayton, North Carolina. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Technical Writer - Onsite in Clayton, NC
This is a pharmaceutical technical writing position focused on developing, revising, and managing GMP documentation that supports manufacturing operations, process engineering, facilities, training, and quality systems. The role is not simply editing documents. The individual serves as a documentation SME and works closely with operations, engineering, learning & development, and quality teams to create and maintain compliant operational procedures and work instructions.
Candidates must be able to work onsite.
Must be eligible to work in the Unite States.
No Corp to Corp candidates please.
What the Person Will Be Doing
The primary responsibility is to create, revise, and manage operational documentation used within a pharmaceutical manufacturing environment, including:
SOPs (Standard Operating Procedures)
Work Instructions
Job Instructions
Controlled documents
Quality management system (QMS) documents
Process and operational standards
Document revisions and remediation activities
The writer will also:
Translate complex manufacturing and production-floor activities into clear written instructions.
Work closely with SMEs and document owners.
Review documents for compliance, readability, consistency, and accuracy.
Manage document revisions through approval workflows.
Support quality and operational improvement initiatives.
Serve as an SOP and documentation subject matter expert.
Technical Environment
This role supports a pharmaceutical manufacturing site and requires understanding of:
GMP requirements
Manufacturing operations
Production processes
Change control systems
Quality systems
Training processes
Lean/process improvement concepts
Major Requirements
Industry Experience
The strongest candidates will have:
Pharmaceutical manufacturing experience
GMP-regulated environment experience
Technical writing experience supporting operations, engineering, manufacturing, facilities, or quality groups
Documentation Experience
Candidates should have experience authoring and managing:
SOPs
Work Instructions
Job Instructions
Quality documents
Change controls
Controlled documents
Change Control Knowledge
The role specifically emphasizes:
Document revision processes
Change control systems
Documentation management
Managing multiple document revisions simultaneously
Supporting active document change controls (DCCs)
Candidates must be comfortable:
Interviewing SMEs
Working with production personnel
Partnering with Quality and Learning & Development teams
Coaching document owners on writing standards
Translating technical manufacturing activities into clear instructions
Ideal Candidate Profile
The ideal candidate is someone who has spent years in pharmaceutical manufacturing organizations supporting:
Process Engineering
Maintenance
Manufacturing Operations
Quality Systems
and has significant experience writing and revising:
SOPs
Maintenance procedures
Equipment-related documentation
Training materials
Manufacturing work instructions
while understanding GMP requirements and controlled document systems.
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Worksite address
clayton, NC, 27520, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.