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Packaging Technical Writer

  • ... Posted on: Feb 16, 2026
  • ... Confidential
  • ... Central Islip, New York
  • ... Salary: Not Available
  • ... Full-time

Packaging Technical Writer   

Job Title :

Packaging Technical Writer

Job Type :

Full-time

Job Location :

Central Islip New York United States

Remote :

No

Jobcon Logo Job Description :

Job Title: Packaging Technical Writer – Pharmaceutical ManufacturingLocation: Central Islip, New York (On-site role)Employment Type: Full-Time | HourlyPay Range: $18.00 – $29.50 per hour (Final pay based on experience, skills, and interview evaluation)Job OverviewWe 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.Key ResponsibilitiesPrepare, review, and revise technical documentation including batch records, specifications, methods, COAs, validation protocols, and reportsSupport packaging investigations, CAPAs, change controls, and deviation documentationConduct focused time studies to support packaging operations and efficiencyApply lean and process improvement tools (5S, Fishbone, Kanban, poka-yoke, visual controls)Review documents for accuracy, clarity, compliance, and correct terminologyPerform data analysis and provide recommendations to improve packaging operationsFollow SOPs for document creation, control, and storageParticipate in root cause analysis and continuous improvement initiativesEnsure compliance with safety, health, and environmental proceduresCollaborate cross-functionally while also working independently when requiredSupport administrative and project-related tasks as assignedRequired QualificationsBA/BS degree in a related field from an accredited institution1–3 years of technical writing experienceExperience in a pharmaceutical or regulated manufacturing environment preferredStrong understanding of cGMPs and FDA guidelinesExcellent written and verbal communication skills in EnglishStrong proficiency in Microsoft Word, Excel, PowerPoint, and PDF editing toolsHigh attention to detail and strong documentation control skillsAbility to manage multiple priorities and meet deadlinesWork Authorization: Candidates must be authorized to work in the United States. (No sponsorship available for this role.)BenefitsHealth, Dental & Vision Insurance401(k) with company matchPaid Time Off & HolidaysShort- and Long-Term DisabilityParental & family leave

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Jobcon Logo Position Details

Posted:

Feb 16, 2026

Employment:

Full-time

Salary:

Not Available

City:

Central Islip

Job Origin:

APPCAST_CPC

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Job Title: Packaging Technical Writer – Pharmaceutical ManufacturingLocation: Central Islip, New York (On-site role)Employment Type: Full-Time | HourlyPay Range: $18.00 – $29.50 per hour (Final pay based on experience, skills, and interview evaluation)Job OverviewWe 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.Key ResponsibilitiesPrepare, review, and revise technical documentation including batch records, specifications, methods, COAs, validation protocols, and reportsSupport packaging investigations, CAPAs, change controls, and deviation documentationConduct focused time studies to support packaging operations and efficiencyApply lean and process improvement tools (5S, Fishbone, Kanban, poka-yoke, visual controls)Review documents for accuracy, clarity, compliance, and correct terminologyPerform data analysis and provide recommendations to improve packaging operationsFollow SOPs for document creation, control, and storageParticipate in root cause analysis and continuous improvement initiativesEnsure compliance with safety, health, and environmental proceduresCollaborate cross-functionally while also working independently when requiredSupport administrative and project-related tasks as assignedRequired QualificationsBA/BS degree in a related field from an accredited institution1–3 years of technical writing experienceExperience in a pharmaceutical or regulated manufacturing environment preferredStrong understanding of cGMPs and FDA guidelinesExcellent written and verbal communication skills in EnglishStrong proficiency in Microsoft Word, Excel, PowerPoint, and PDF editing toolsHigh attention to detail and strong documentation control skillsAbility to manage multiple priorities and meet deadlinesWork Authorization: Candidates must be authorized to work in the United States. (No sponsorship available for this role.)BenefitsHealth, Dental & Vision Insurance401(k) with company matchPaid Time Off & HolidaysShort- and Long-Term DisabilityParental & family leave

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