The Technical Document Writer will be responsible for producing high-quality cGMP documentation that contributes to the overall success of our project goals. Additional responsibilities might include ...
The Technical Document Writer will be responsible for producing high-quality cGMP documentation that contributes to the overall success of our project goals. Additional responsibilities might include ...
The Advanced Planning Writer develops Advanced Planning Documents, Medicaid Detail Budget Tables and other documentation required for the planning, implementation, and operations activities in ...
The Advanced Planning Writer develops Advanced Planning Documents, Medicaid Detail Budget Tables and other documentation required for the planning, implementation, and operations activities in ...
Develop/maintain design documentation and information provided by subject matter experts in the engineering and service functions. Integrate relevant information into well written text instructions ...
Develop/maintain design documentation and information provided by subject matter experts in the engineering and service functions. Integrate relevant information into well written text instructions ...
Technical Writer Location: Santa Clara CA 95054 Duration: 06+ months (Possibilities of extension) Qualifications Looking for a Technical Writer with 7 - 9 Years of Experience, at least 3 years in ...
Technical Writer Location: Santa Clara CA 95054 Duration: 06+ months (Possibilities of extension) Qualifications Looking for a Technical Writer with 7 - 9 Years of Experience, at least 3 years in ...
Advanced Planning Document Writer Raleigh NC/REMOTE 6+ months Description: The Division of Health Benefits, NC Medicaid, Advanced Planning Office is seeking an APD Writer with experience in ...
Advanced Planning Document Writer Raleigh NC/REMOTE 6+ months Description: The Division of Health Benefits, NC Medicaid, Advanced Planning Office is seeking an APD Writer with experience in ...
Director Medical Writing - AI Document Lead
Boston, MA · On-site
$220K - $260K/yr
Position Summary We are seeking an experienced medical writer with deep expertise in clinical and regulatory documents and demonstrated experience using AI-enabled tools to support the development ...
Director Medical Writing - AI Document Lead
Boston, MA · On-site
$220K - $260K/yr
Position Summary We are seeking an experienced medical writer with deep expertise in clinical and regulatory documents and demonstrated experience using AI-enabled tools to support the development ...
Responsibilities The contract writer will be responsible for drafting and reviewing documentation related to but not limited to, procurement activities, such as purchase orders, service agreements ...
Responsibilities The contract writer will be responsible for drafting and reviewing documentation related to but not limited to, procurement activities, such as purchase orders, service agreements ...
Create and revise flight documents (Airplane Flight Manual, Pilot's Abbreviated Checklists ... Detail focused and well organized with excellent verbal and written communication skills.
Create and revise flight documents (Airplane Flight Manual, Pilot's Abbreviated Checklists ... Detail focused and well organized with excellent verbal and written communication skills.
Experience with electronic document management and database systems preferred.
Experience with electronic document management and database systems preferred.
... document change requests. • Work with internal teams to obtain an in-depth understanding of the ... the writing team. • Plan and conduct work requiring independent judgment in the evaluation ...
... document change requests. • Work with internal teams to obtain an in-depth understanding of the ... the writing team. • Plan and conduct work requiring independent judgment in the evaluation ...
Completion of formal professional or technical writing courses. The ideal candidate combines ... documentation that supports readiness across the system lifecycle.
Completion of formal professional or technical writing courses. The ideal candidate combines ... documentation that supports readiness across the system lifecycle.
Technical Documentation SME
Bedford, IN · On-site
Completion of formal professional or technical writing courses. The ideal candidate combines ... documentation that supports readiness across the system lifecycle. Overview SAIC accepts ...
Technical Documentation SME
Bedford, IN · On-site
Completion of formal professional or technical writing courses. The ideal candidate combines ... documentation that supports readiness across the system lifecycle. Overview SAIC accepts ...
General Characteristics The contract writer will be responsible for drafting and reviewing documentation related to but not limited to, procurement activities, such as purchase orders, service ...
General Characteristics The contract writer will be responsible for drafting and reviewing documentation related to but not limited to, procurement activities, such as purchase orders, service ...
Contract Writer The contract writer will be responsible for drafting and reviewing documentation related to but not limited to, procurement activities, such as purchase orders, service agreements ...
Contract Writer The contract writer will be responsible for drafting and reviewing documentation related to but not limited to, procurement activities, such as purchase orders, service agreements ...
Document Controller & Technical Writer
Indianapolis, IN · On-site
$18 - $20/hr
The Document Controller & Technical Writer will engage with internal customers to provide records management and related support to the business site. Responsibilities include a broad range of ...
Quick apply
Document Controller & Technical Writer
Indianapolis, IN · On-site
$18 - $20/hr
The Document Controller & Technical Writer will engage with internal customers to provide records management and related support to the business site. Responsibilities include a broad range of ...
Document Control - Technical Writer I
Greenup, IL · On-site
$53K - $62K/yr
Document Control - Technical Writer I Responsibilities The Document Control - Technical Writer I is responsible for creation, review, control, distribution, and timeliness of documents that will be ...
Document Control - Technical Writer I
Greenup, IL · On-site
$53K - $62K/yr
Document Control - Technical Writer I Responsibilities The Document Control - Technical Writer I is responsible for creation, review, control, distribution, and timeliness of documents that will be ...
Ability to deliver high quality documentation paying attention to detail Ability to quickly grasp ... pictures Excellent written skills in English Strong working knowledge of Microsoft Office to ...
Ability to deliver high quality documentation paying attention to detail Ability to quickly grasp ... pictures Excellent written skills in English Strong working knowledge of Microsoft Office to ...
Creative document writing experience - * Experience with numbers/data (metrics) * GMP experience Technical Writer does: * Understands validation concepts in order to produce documentation for ...
Creative document writing experience - * Experience with numbers/data (metrics) * GMP experience Technical Writer does: * Understands validation concepts in order to produce documentation for ...
Senior Technical Documentation Writer/Specialist II
Greenville, NC · On-site
$27 - $28/hr
Under limited direction, the SR Tech Writer leads tasks related to documenting and developing detailed operation, maintenance, and troubleshooting procedures, checklists, technical specifications ...
Senior Technical Documentation Writer/Specialist II
Greenville, NC · On-site
$27 - $28/hr
Under limited direction, the SR Tech Writer leads tasks related to documenting and developing detailed operation, maintenance, and troubleshooting procedures, checklists, technical specifications ...
Senior Technical Documentation Writer/Specialist II
Greenville, NC · Hybrid
$27 - $28/hr
Under limited direction, the SR Tech Writer leads tasks related to documenting and developing detailed operation, maintenance, and troubleshooting procedures, checklists, technical specifications ...
Senior Technical Documentation Writer/Specialist II
Greenville, NC · Hybrid
$27 - $28/hr
Under limited direction, the SR Tech Writer leads tasks related to documenting and developing detailed operation, maintenance, and troubleshooting procedures, checklists, technical specifications ...
Document Writer information
See salary details
$20.91 - $23.93
22% of jobs
$24.34 is the 25th percentile. Wages below this are outliers.
$23.93 - $26.94
21% of jobs
The median wage is $29.12 / hr.
$26.94 - $29.96
9% of jobs
$29.96 - $32.98
1% of jobs
$32.98 - $35.99
2% of jobs
$35.99 - $39.01
13% of jobs
$39.01 - $42.02
2% of jobs
$42.02 - $45.04
1% of jobs
$45.04 - $48.06
1% of jobs
$48.81 is the 75th percentile. Wages above this are outliers.
$48.06 - $51.07
9% of jobs
$51.07 - $54.09
18% of jobs
$20
$35
$54
How much do document writer jobs pay per hour?
Is there still a demand for writers?
What is the highest paying job for writers?
How much do documentation writers make?
What are the key skills and qualifications needed to thrive as a Document Writer, and why are they important?
What are some common challenges faced by Document Writers when working with subject matter experts (SMEs)?
What does a documentation writer do?
What does a Document Writer do?
- Sop Technical Writer
- Technical Writer Pharmaceutical Industry
- Technical Writer I
- Saturday Technical Documentation Writer
- Volunteer Technical Documentation Writer
- Work From Home Condition Report Writer
- Remote Compliance Technical Writer
- Contract Writing
- Online Military Technical Writer
- Remote Software Technical Writer

Contractor
Medical, Dental, Vision, Life, Retirement, PTO
Posted 14 days ago
Job description
Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs.
Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance.
Description:
We are currently looking for a cGMP Technical Writer who will be responsible for writing, reviewing and driving production and quality documentation to approval.
The Technical Document Writer will be responsible for producing high-quality cGMP documentation that contributes to the overall success of our project goals.
Additional responsibilities might include tracking of the daily, weekly and monthly forecasted documentation priorities required to meet output quotas.
Key responsibilities/essential functions:
Originate, revise and maintain Standard Operating Procedures (SOPs), Production Batch Records (PBRs) and Solution Preparation Records.
Compile and draft procedural documentation using standard electronic publishing tools.
Create and maintain templates for cGMP documents.
Collaborate with individuals from various internal functional areas to generate and review new equipment, processing, set-up and operational documents within agreed upon timelines.
Interview subject matter experts to obtain details in order to accurately capture content material.
Demonstrate effective written and verbal communication skills.
Monitor the flow of production documents and adjust workload and resources in an appropriate, organized and efficient manner.
Work with cross-functional teams on the implementation of process improvement initiatives to increase quality in cGMP documentation.
Demonstrate an ability to multi-task and manage multiple projects independently
Maintain a safe work environment for self and staff.
Quality Specific Goals:
Aware of and comply with the client Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position.
Complete all planned Quality & Compliance training within the defined deadlines.
Identify and report any quality or compliance concerns and take immediate corrective action as required.
Aware of and comply with Stop Order, Concessions, ESD ECO, Calibration, Preventative Maintenance, Material Identification & Segregation, and Good Documentation Practices, as associated with this job type/position.
Training: Aware of and comply with client training requirements.
Required Qualifications:
3+ years of previous technical writing experience in a cGMP pharmaceutical environment.
Experience in manufacturing under cGMP guidelines and possess a strong knowledge of cGMP requirements.
Prior experience working in a biotech/pharmaceutical company.
Exceptional written/verbal communication, listening, organizational, interpersonal, research, investigative, and problem-solving skills.
Proven ability to communicate complex ideas in a clear, concise manner.
Working knowledge of MS Office Suite and an Electronic Document Management System (EDMS).
Experience with Document Proficiency in MS Office Products.
Preferred Qualifications:
Associates degree in a scientific discipline or equivalent experience.
Cell Culture experience.
Protein Purification experience.
Biological Technical Transfer experience.
To know more about this position please contact after applying to the position on;
Ujjwal Mane
ujwal.mane(at)collabera.com
973-805-7557