Packaging Technical Writer

Overview

Job Title:
Packaging Technical Writer – Pharmaceutical Manufacturing

Location: Central Islip, New York (On-site role)

Employment Type: Full-Time | Hourly

Pay Range: $18.00 – $29.50 per hour

(Final pay based on experience, skills, and interview evaluation)

We are seeking a Packaging Technical Writer to support documentation, process improvement, and compliance activities within a pharmaceutical packaging environment
. This role focuses on preparing, reviewing, and maintaining technical documentation in accordance with cGMP and FDA guidelines
, while collaborating closely with packaging, quality, and manufacturing teams.

This is an on-site position based in Central Islip, NY.

• Prepare, review, and revise technical documentation including batch records, specifications, methods, COAs, validation protocols, and reports
• Support packaging investigations, CAPAs, change controls, and deviation documentation
• Conduct focused time studies to support packaging operations and efficiency
• Apply lean and process improvement tools (5S, Fishbone, Kanban, poka-yoke, visual controls)
• Review documents for accuracy, clarity, compliance, and correct terminology
• Perform data analysis and provide recommendations to improve packaging operations
• Follow SOPs for document creation, control, and storage
• Participate in root cause analysis and continuous improvement initiatives
• Ensure compliance with safety, health, and environmental procedures
• Collaborate cross-functionally while also working independently when required
• Support administrative and project-related tasks as assigned

• BA/BS degree in a related field from an accredited institution
• 1–3 years of technical writing experience
• Experience in a pharmaceutical or regulated manufacturing environment preferred
• Strong understanding of cGMPs and FDA guidelines
• Excellent written and verbal communication skills in English
• Strong proficiency in Microsoft Word, Excel, PowerPoint, and PDF editing tools
• High attention to detail and strong documentation control skills
• Ability to manage multiple priorities and meet deadlines

Candidates must be authorized to work in the United States
.

(No sponsorship available for this role.)