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Full Time Compliance Technical Writer Jobs (NOW HIRING)

Manifest Solutions is currently seeking a Senior Compliance Technical Writer for a position in Columbus, OH. * Prepare, edit, and maintain NERC compliance documentation, including: Procedures ...

Manifest Solutions is currently seeking a Senior Compliance Technical Writer for a position in Columbus, OH. * Prepare, edit, and maintain NERC compliance documentation, including: Procedures ...

In this role, you will develop clear, accurate, and compliant technical documentation that enables ... Employment Type: FULL_TIME

In this role, you will develop clear, accurate, and compliant technical documentation that enables ... Employment Type: FULL_TIME

In this role, you will develop clear, accurate, and compliant technical documentation that enables ... Employment Type: FULL_TIME

In this role, you will develop clear, accurate, and compliant technical documentation that enables ... Employment Type: FULL_TIME

... Quality, Compliance, Technical Operations o Network Customers Resources Managed- Financial ... writing, preferably in a pharmaceutical or related environment AS in Communications or related ...

Technical Writer

Lexington, MA ยท On-site

$69K - $158K/yr

... clear, compliant technical content * Ability to pay strict attention to detail, and display ... Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible ...

Job Type Full-time Description If you are looking for an exciting career opportunity in the ... an ISO 9001-compliant Quality Management System (QMS). General Skillset * Proficiency with ...

... compliance. In this role, you will work closely with senior technical writers, analysts, engineers, and operational personnel to gather information, draft documentation, and support production of ...

... Management & Compliance Business Continuity & Disaster Recovery Security & Privacy Specialties ... Technical Writer Job Details Researches, analyzes, designs, develops, writes, edits, and publishes ...

Requisition ID2026-4576Job Summary Artemis is seeking a full-time Technical Writer to support the ... Maintain compliance with Section 508 accessibility requirements and manage copyright permissions ...

... compliant technical content. This role supports document development across the equipment life ... Strong written and verbal communication skills with the ability to coordinate directly with ...

Fulltime, On-site, Quantico, VA; limited travel as required ( Role Overview: The Technical Writer ... an ISO 9001-compliant Quality Management System (QMS). General Skillset * Proficiency with ...

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Full Time Compliance Technical Writer information

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How much do full time compliance technical writer jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for full time compliance technical writer in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

What does a full time compliance technical writer do?

A Full Time Compliance Technical Writer is responsible for creating, editing, and maintaining documentation that ensures a company adheres to industry regulations and internal policies. They work closely with compliance officers, legal teams, and subject matter experts to translate complex regulatory requirements into clear and accessible documents, such as manuals, policies, and training materials. Their work helps organizations avoid legal risks, pass audits, and educate employees on compliance standards. Attention to detail and strong communication skills are essential in this role.

What are the key skills and qualifications needed to thrive as a full time compliance technical writer, and why are they important?

To thrive as a Full Time Compliance Technical Writer, you need strong writing, editing, and document management skills, often supported by a degree in English, Communications, or a related field. Familiarity with regulatory frameworks (such as ISO, FDA, or GDPR), document control systems, and technical writing tools like Adobe FrameMaker or MadCap Flare is typically required. Outstanding attention to detail, analytical thinking, and the ability to communicate complex information clearly are critical soft skills. These abilities ensure that documentation is accurate, compliant, and accessible, supporting organizational adherence to regulations and reducing risk.

What are some common challenges faced by full time compliance technical writers when working with cross-functional teams?

Full Time Compliance Technical Writers often collaborate with legal, engineering, and operations teams to ensure that documentation meets regulatory standards. One common challenge is translating complex legal or technical language into clear, user-friendly documents while maintaining accuracy and compliance. Balancing multiple stakeholder inputs and adhering to tight deadlines can also be demanding. Effective communication and project management skills are essential to navigate these challenges and ensure that all documentation aligns with both organizational goals and regulatory requirements.

What is the difference between Full Time Compliance Technical Writer vs Regulatory Documentation Specialist?

AspectFull Time Compliance Technical WriterRegulatory Documentation Specialist
CredentialsTypically requires technical writing certifications, compliance knowledge, and industry-specific trainingOften requires regulatory affairs certifications and technical writing skills
Work EnvironmentWorks in corporate, healthcare, or manufacturing settings, producing compliance manuals and proceduresWorks in regulated industries like pharmaceuticals or biotech, preparing regulatory submissions and documentation
Employer & Industry UsageCommon in industries with strict compliance standards, such as healthcare, finance, and manufacturingPrimarily found in pharmaceutical, biotech, and medical device companies

While both roles involve technical writing and compliance, the Full Time Compliance Technical Writer focuses on creating internal compliance documents, whereas the Regulatory Documentation Specialist primarily prepares documents for regulatory submissions. Both require strong writing skills and industry knowledge but serve different purposes within regulated industries.

More about Full Time Compliance Technical Writer jobs

What cities are hiring for Full Time Compliance Technical Writer jobs?

Cities with the most Full Time Compliance Technical Writer job openings:

What are the most commonly searched types of Compliance Technical Writer jobs?

The most popular types of Compliance Technical Writer jobs are:

What states have the most Full Time Compliance Technical Writer jobs?

States with the most job openings for Full Time Compliance Technical Writer jobs include:

Infographic showing various Full Time Compliance Technical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, and 4% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.

Sr. Operations Compliance, Technical Writer

Corden Pharma Colorado

Boulder, CO โ€ข On-site

$93K - $116K/yr

Full-time

Medical, Dental, Life, Retirement

Posted 14 days ago


Job description

CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in active pharmaceutical ingredients (APIs), excipients, drug products (DPs), and packaging. With around 3,000 employees worldwide, we help pharmaceutical and biotech companies manufacture medicines with the ultimate goal of improving people’s lives.


Our network, spanning Europe and the U.S., provides flexible and specialized solutions across six technology platforms: Peptides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules, and Oligonucleotides. We strive for excellence in supporting this network and are committed to delivering the highest quality products for patient well-being.

 

Our People Vision

We strive for excellence. We share our passion. Together, we make a difference in patients' lives.


SUMMARY

The Sr. Operations Compliance, Technical Writer acts as the primary resource for authorship of procedures and technical documents used or in support of the Operations and Technical Operations Department (e.g., standard operating procedures, training documentation, change controls, risk assessments, gap assessments, maintenance documentation, batch records, specifications, test methods, protocols, reports etc.) to support the manufacture of intermediate and API drug substances. In this role, the Sr. Technical Writer is responsible for ensuring that these documents are delivered on time, in a compliant fashion, and to the standards expected by the teams that own, execute, and use the documents.


ESSENTIAL DUTIES AND RESPONSIBILITIES

Include the following. Other duties may be assigned.


  • Establishes and maintains strong, transparent, and effective day-to-day working relationships between Manufacturing, R&D, regulatory groups, and internal and external customers related to assigned duties
  • Ensures the generation of Operations and Technical Operational documents are executed to the planned timing and quality deliverables
  • Works closely with departments summarized above to create documentation that meets the regulatory/compliance and manufacturing requirements directly related to the products produced and equipment operated at Corden Pharma Colorado
  • Responsible for the efficient transition of process documentation generated from the laboratory (or customer documentation) into the proper format and language used at CPC manufacturing facilities. Ensures technical requirements for the process are maintained. Advises other departments on the proper level of detail required for the effort at hand, ensuring that the appropriate content is included to meet the project or process deliverables 
  • Serves as a technical lead on documentation/projects and ensures required supporting actions are identified to support the project implementation
  • Participates in programs to plan, execute, review, and improve document generation business processes at CPC. Identifies opportunities for improvement based on customer need, best industry practices, and the need for internal continuous improvement
  • Identifies and drives opportunities to implement process improvements and facilitates implementation of the identified improvements through updates to necessary documentation/procedures
  • Supports and provides technical guidance on documents/procedures with other departments and technical writers
  • When workload permits, assists with document generation in other departments as needed
  • Supports or author’s investigations, deviations, CAPAs, change controls, etc. 
  • Implements and maintains adherence as a technical expert to all company policies concerning Safety, Health, & Environment (SHE), Quality, and Human Resources 

LEADERSHIP & BUDGET RESPONSIBILITIES

Provides guidance and leadership in the generation of the regulatory/compliance and manufacturing documentation related to all commercial and development products manufactured. Uses technical knowledge of equipment, processes, cGMPs, and regulatory filings to provide direction to the development teams, technical teams, and Operations in the generation of Operations procedures.


EDUCATION and/or EXPERIENCE

Bachelor's Degree (BA or BS) from a 4-year college or university; or 5 years related experience in the technical writing of regulatory/compliance and cGMP manufacturing documentation; or an equivalent combination of education and experience. Previous experience in a technical role recommended (for example, analytical chemist, process engineer etc.).


CERTIFICATES, LICENSES, REGISTRATIONS

None.


CORE COMPETENCIES

These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity.


  • Results oriented approach to process performance
  • Excellent organizational, writing, communication, and computer skills
  • Knowledge of analytical equipment in both Quality Control and Development (R&D) environments and/or knowledge of chemical manufacturing process, and an in-depth knowledge of cGMP Quality Systems
  • Technical writing which allows documents to be clearly followed and understood by end users
  •  Advanced skills in publishing software (e.g., Microsoft Word, Microsoft Visio, Adobe FrameMaker, etc.)
  • Demonstrated ability to prioritize incoming work, work assignments, and to meet deadlines
  • Ability to build relationships and influence and motivate others
  • Ability to achieve results through the positive direction of others
  • Technical expertise in the practices and technologies used in peptide and HPAPI manufacturing, and the ability to use these skills in active projects
  • Knowledge of chemical processing, plant equipment, and infrastructure
  • Working knowledge of regulatory compliance issues in pharmaceutical manufacturing
  • Planning, implementation, facilitation and follow-up skills
  • Knowledge of applicable regulatory requirements with the ability to apply this knowledge independently with minimal input from a supervisor/manager 
  • Supports customer communications
SALARY

Actual pay will be based on your skills and experience.

 BENEFITS
  • 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service 
  • Accident Plan
  • Critical Illness
  • Dental Insurance
  • Disability Insurance
  • Employee Assistance Program
  • Flexible Spending Account
  • Health Insurance PPO/HSA
  • Hospital Indemnity Plan
  • ID Theft
  • Life Insurance
  • Paid Parental Leave
  • Tuition Reimbursement
  • Wellness Program
  • Vacation – Three Weeks 1st Year
EQUAL OPPORTUNITY EMPLOYER

Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices.


This post will expire September 18, 2026