Top 10 Technical writer Jobs in Cranbury Nj

Senior Technical Writer
Orion Group —Somerville, NJ
- $23 - $28 an hour
- Full-time
- Microsoft Word
- 3 years
- Bachelor's degree
- Health insurance
- Dental insurance
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7d
Cybersecurity Technical Writer - AI Trainer
DataAnnotation —New Jersey
- $50 - $100 an hour
- Part-time
- Remote
- English
- Mid-level
- Bachelor's degree
- Flexible schedule
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Technical Writer - Operations
Experic LLC —Cranbury, NJ
- $80,000 - $110,000 a year
- Mid-level
- Office
- 3 years
Quick Apply
Documentation and Training Specialist
Princeton Plasma Physics Laboratory —Princeton, NJ
- $93,400 - $149,200 a year
- Full-time
- Mentoring
- Senior level
- Associate's degree
- On-the-job training
Senior Technical Writer
Software Technology Inc —Trenton, NJ
- Hybrid work
- Computer Science
- AWS
- Bachelor's degree
Quick Apply
Technical Operations Scientist
Lupin Pharmaceuticals Inc. —Somerset, NJ
- $70,000 - $95,000 a year
- Full-time
- Engineering
- Mid-level
- 3 years
QA Investigations / Technical Writer
KVK Tech —Newtown, PA
- Mid-level
- 3 years
- Master's degree
- Paid holidays
- Dental insurance
Associate Medical Writer - Oncology
BOLDSCIENCE —New Brunswick, NJ
- Medicine
- Doctor of Philosophy
- Quality control
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Senior Technical Writer

Orion Group
Somerville, NJ

Quick Apply

Job Details

Full-time | Contract
$23 - $28 an hour
7 days ago

Benefits

Health insurance
Dental insurance
Vision insurance
401(k) matching
401(k) 2% match

Qualifications

Technical editing
Microsoft Word
Content creation for technical audiences
Document control experience within pharmaceutical industry
ISO standards
Pharmaceutical regulatory compliance
Word embeddings
Technical writing experience within manufacturing
Manufacturing standard operating procedures
Bachelor's degree
Compliance documentation
Technical writing
Biomedical regulatory compliance
Technical writing quality assurance
Quality systems
Production batch record review
Achieving project delivery timelines
Grammar Experience
Standard operating procedures (SOPs)
Content review
Project stakeholder communication
Cross-functional communication
FDA regulations
Standard operating procedures drafting

Full Job Description

Senior Technical Writer – Quality Documentation & Change Control

Location: 100% Onsite- Branchburg, NJ
Industry: Pharmaceutical / Medical Device / Biotechnology

Contract through the end of 2026 with potential extensions

Up to $28/hr based on benefit elections

About the Role

Orion Group is seeking an experienced Senior Technical Writer – Quality Documentation & Change Control to support the development, creation, revision, and management of controlled documentation within a highly regulated pharmaceutical manufacturing environment.

This role will author and revise SOPs, work instructions, batch records, forms, and other controlled documents while partnering closely with Manufacturing, Engineering, Process Development, Quality, CAPA/Investigations, Change Control, and other subject matter experts.

The ideal candidate has hands-on technical writing experience within pharmaceutical, biotechnology, or medical device environments and understands how to translate complex technical processes into clear, accurate, compliant documentation.

Key Responsibilities

Author, revise, edit, and maintain controlled documentation, including:
Standard Operating Procedures (SOPs)
Work Instructions
Batch Records
Forms and other GMP-controlled documentation
Serve as an Initiator for Change Controls and manage activities through completion while working against tight deadlines.
Gather technical information from subject matter experts and translate complex processes into clear, straightforward procedures.
Ensure documents contain the appropriate level of detail and accurately reflect process and product specifications.
Serve as an SME for document creation, formatting, revision, and Electronic Document Management System (EDMS) processes.
Process controlled documentation within the EDMS in accordance with established policies and procedures.
Review and evaluate change requests of varying complexity and support activities required for timely closure.
Partner with Manufacturing, Engineering, Process Development, Quality, CAPA/Investigations, Change Control, and other cross-functional teams to develop and revise document content.
Proofread and edit technical documentation for accuracy, consistency, grammar, formatting, and compliance.
Support continuous improvement initiatives related to document management and documentation processes.
Develop and deliver training and guidance to change initiators and support staff.
Represent Quality Documentation and Change Control during regulatory audits.
Communicate project status, risks, and documentation issues to management and escalate concerns when appropriate.
Provide team leadership and guidance as needed and support Change Control leadership in their absence.

Qualifications

Bachelor's degree or 5–7 years of equivalent relevant professional experience.
3–5 years of technical writing experience within a pharmaceutical, medical device, biotechnology, or similarly regulated environment.
Demonstrated experience authoring and revising SOPs, work instructions, batch records, forms, and controlled documentation.
Working knowledge of GMP/GxP requirements and regulated Quality Systems.
Basic knowledge of applicable regulations and standards, including 21 CFR Part 820, ISO 13485, FDA requirements, and AATB standards.
Strong experience working within an Electronic Document Management System (EDMS); One Vault experience is highly preferred.
Experience with SAP or another ERP system preferred.
Advanced Microsoft Word skills, including tables, headers/footers, formatting, document review, and revision capabilities.
Strong proofreading, editing, grammar, and technical writing skills.
Ability to gather information from technical SMEs and convert complex processes into clear, usable documentation.
Strong organizational and project management capabilities with the ability to manage multiple priorities and tight deadlines.
Excellent written, verbal, and interpersonal communication skills.
Ability to work effectively with cross-functional stakeholders at varying levels of the organization.
Experience providing training or guidance related to controlled documentation and change control processes is preferred.

What We're Looking For

The strongest candidate will bring a combination of technical writing expertise and Quality Systems knowledge. This is not simply a general writing position — we're looking for someone who understands controlled documentation within a regulated environment and can confidently work with technical SMEs to ensure documentation is accurate, detailed, compliant, and completed on schedule.

Key Skills:
Technical Writing SOP Authoring Controlled Documentation Change Control EDMS GMP/GxP 21 CFR 820 ISO 13485 Batch Records Work Instructions Quality Systems Microsoft Word SAP Document Control Pharmaceutical / Medical Device / Biotech

Pay: $23.00 - $28.00 per hour

Benefits:

401(k) 2% match
Dental insurance
Health insurance
Vision insurance

Education:

Bachelor's (Preferred)

Experience:

Technical writing: 3 years (Preferred)
Pharmaceutical Industry : 3 years (Preferred)
SAP: 1 year (Preferred)
Quality systems: 3 years (Preferred)

Work Location: In person

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Refine Your Search

technical writer jobs in cranbury nj

Senior Technical Writer

Cybersecurity Technical Writer - AI Trainer

Technical Writer - Operations

Documentation and Training Specialist

Senior Technical Writer

Technical Operations Scientist

QA Investigations / Technical Writer

Associate Medical Writer - Oncology

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