Top 223 technical writer (remote) Jobs in remote

SOP Technical Writer
Medasource —Remote
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- Contract
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- Bachelor's degree
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- Health insurance
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Freelance Proposal Technical Writer(Remote)
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Technical Documentation Specialist, Military Personnel & Family Research
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1d
Technical Writer
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SOP Technical Writer

Medasource -
Remote

Quick Apply

Job Details

Contract
$40 - $50 an hour

Benefits

Health insurance
Dental insurance
Vision insurance

Qualifications

Technical editing
Biology
Teamwork
Content creation for technical audiences
Document control within pharmaceutical industry
Regulatory reporting
Technical writing within manufacturing
Factory operations documentation
Manufacturing standard operating procedures
Manufacturing facility
Bachelor's degree
Attention to detail
Pharmaceutical company experience
Compliance documentation
Organizational skills
Technical writing
Collaboration with manufacturing teams
Technical writing quality assurance
Quality systems
Standard operating procedures (SOPs)
Cross-functional communication
Standard operating procedures drafting
Pharmaceutical manufacturing facility experience

Full Job Description

Job Title: SOP Technical Writer

Contract Length: 3-months

Location: Remote

Hours: 40 hours per week

Start Date: 7/6/26

Client Overview:

Our client is a global animal health company focused on developing and delivering innovative products and services that prevent and treat disease in farm animals and pets. Operating in a highly regulated, GMP-driven environment, our client emphasizes quality, compliance, and operational excellence across its manufacturing and research sites worldwide. The organization partners closely with veterinarians, producers, and pet owners to improve animal health, food safety, and overall wellbeing.

Overview:

Our client is seeking an experienced SOP Technical Writer to support a manufacturing documentation initiative within a regulated animal health/pharmaceutical manufacturing environment. This individual will partner cross-functionally with Manufacturing Operations, Quality, Manufacturing Process teams, and Documentation Control to support updates and revisions to existing controlled documents and workflows across the facility.

This role will focus primarily on revising and maintaining existing SOPs, work instructions, and manufacturing documentation to support operational efficiency, compliance, and document standardization initiatives.

Key Responsibilities

Revise, edit, and maintain SOPs, work instructions, manufacturing procedures, and controlled GMP documentation
Collaborate with Manufacturing, Quality, and Process SMEs to incorporate identified procedural updates and workflow changes
Support documentation remediation and continuous improvement initiatives across multiple manufacturing groups
Coordinate document revisions through review, feedback, and approval workflows
Ensure documentation aligns with GMP, regulatory, and internal quality standards
Manage document versioning, formatting consistency, and change tracking
Facilitate communication between cross-functional stakeholders throughout the document lifecycle
Work within electronic document management systems and quality systems to route and manage documentation updates
Support expedited turnaround of documentation updates while maintaining strong attention to detail and compliance standards

Required Qualifications

Bachelor’s degree in Life Sciences, Biology, Chemistry, Biotechnology, Pharmaceutical Sciences, Engineering, Technical Communications, or a related scientific/technical field
5+ years of SOP Technical Writing experience within a regulated manufacturing environment
Experience supporting GMP-regulated pharmaceutical, biotech, medical device, or animal health manufacturing operations
Strong understanding of manufacturing processes and quality systems
Experience revising and maintaining controlled documentation and SOPs
Ability to work cross-functionally with Manufacturing, Quality, Validation, and Process teams
Strong written communication and document editing skills
Exceptional attention to detail and organizational skills
Ability to manage multiple document workflows simultaneously

Preferred Qualifications

Advanced degree or technical certification related to Quality, Regulatory Affairs, Technical Writing, or Life Sciences preferred
Animal health industry experience
USDA-regulated environment experience
Pharmaceutical manufacturing background
Experience with Veeva Vault QualityDoc or similar document management systems
Experience supporting documentation review and approval workflows
Prior experience supporting manufacturing operations or process improvement initiatives
Collaborative and responsive communicator
Able to work effectively with multiple stakeholder groups
Comfortable navigating review cycles and incorporating feedback
Self-directed and able to manage priorities independently
Strong sense of ownership and urgency
High attention to detail with a focus on minimizing rework and documentation errors

Pay: $40.00 - $50.00 per hour

Benefits:

Dental insurance
Health insurance
Vision insurance

Education:

Bachelor's (Preferred)

Experience:

SOP : 5 years (Preferred)
Technical writing: 5 years (Preferred)
Regulatory reporting: 5 years (Preferred)

Work Location: Remote

Quick Apply

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