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Director Engineering Technical Writer Jobs in Iowa

Technical Writing Tutor

Ames, IA · Remote

$18 - $40/hr

Emphasizes clarity, conciseness, and accuracy in conveying complex information and connects technical writing to software development, engineering, healthcare, and scientific communication ...

Emphasizes clarity, conciseness, and accuracy in conveying complex information and connects technical writing to software development, engineering, healthcare, and scientific communication ...

Workiva is seeking a Director of GTM Technical Delivery who is equal parts technical visionary and ... You will lead developers, admins, QA, and DevOps professionals responsible for the systems that ...

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Director Engineering Technical Writer information

What is the difference between Director Engineering Technical Writer vs Technical Writer?

AspectDirector Engineering Technical WriterTechnical Writer
CredentialsBachelor's or higher in Engineering, Technical Communication, or related field; extensive experienceBachelor's in Communications, English, or related field; some experience preferred
Work EnvironmentLeads teams in engineering or tech companies, overseeing documentation strategyCreates technical content individually or in small teams, often in various industries
Employer & Industry UsageCommon in tech, engineering, and manufacturing firmsWidely used across tech, healthcare, finance, and other sectors

The main difference is that the Director Engineering Technical Writer oversees documentation teams and strategy, focusing on high-level management and coordination. In contrast, a Technical Writer primarily produces technical content, often working independently or in small teams. Both roles require strong technical knowledge, but the director role emphasizes leadership and strategic planning.

Are technical writers in demand?

Technical writers, including those in engineering roles, are in steady demand due to the need for clear documentation of complex technical information. Employers seek professionals skilled in tools like Markdown and Adobe FrameMaker, often requiring certifications or experience with industry-specific standards. The demand is expected to grow as technology advances and companies prioritize effective communication.

What is the highest salary for a technical writer?

The highest salaries for technical writers, including those in engineering roles, can exceed $100,000 annually, especially for senior or specialized positions with extensive experience, advanced skills, or in high-demand industries. Factors such as location, certifications, and technical expertise influence top-tier compensation.

What does an engineering technical writer do?

An engineering technical writer creates clear, detailed documentation such as manuals, guides, and technical reports for engineering products and processes. They work closely with engineers to understand complex technical information and often use tools like Adobe FrameMaker or MadCap Flare to produce accurate, user-friendly content. Strong writing skills and technical knowledge are essential for this role.

Is technical writing replaced by AI?

Technical writing, including roles like a Director of Engineering Technical Writer, involves creating clear, detailed documentation that often requires human expertise and understanding of complex concepts. While AI tools can assist with drafting, editing, and generating content, they do not fully replace the critical thinking, context awareness, and nuanced communication skills of professional technical writers. Human oversight remains essential to ensure accuracy and clarity in technical documentation.
What are the most commonly searched types of Engineering Technical Writer jobs in Iowa? The most popular types of Engineering Technical Writer jobs in Iowa are:
What are popular job titles related to Director Engineering Technical Writer jobs in Iowa? For Director Engineering Technical Writer jobs in Iowa, the most frequently searched job titles are:

Analytical Development Technical Writer

Cambrex

Charles City, IA • On-site

Full-time

Medical, Life, Retirement

Posted 25 days ago


Cambrex rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

37th of 86 rated pharmaceutical


Job description

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. 

With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs.

Your Work Matters.

At Cambrex, we strive to build a culture where all colleagues have the opportunity to:

  • engage in work that matters to our customers and the patients they serve
  • learn new skills and enjoy new experiences in an engaging and safe environment
  • strengthen connections with coworkers and the community

We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company.  We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!

Your Future Matters.

Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!

Overview:

The AD Technical Writer will be responsible for consistently generating high quality technical documents, such as test procedures, protocols, and reports based on data collected by other members of the Analytical Development department that meet the needs of other departments, clients, and regulators.  Compliance with SOPs, cGMP, ICH, and other regulatory guidelines is required to perform most job tasks. 

Responsibilities:
  • Drafting and revising controlled documents such as test procedures, method evaluation protocols, reports, and SOPs while following established guidelines for correctness, completeness, clarity, and format. 
  • Coordinate the approvals of these documents through the use of software such as MasterControl and TrackWise. 
  • Compile and present data from multiple sources such as laboratory notebooks and various laboratory instrumentation software. 
  • Maintain open communication with members of AD, QC, and QA to ensure timely delivery of high quality documents to support evolving business needs. 
  • Continuously improve documentation systems to increase efficiency and compliance with cGMP and/or other regulatory requirements.  

All employees are required to adhere to EPA, DEA, FDA and cGMP regulations as they relate to the operation of the Company; and to adhere to all company safety rules and procedures.  All employees are expected to report to work regularly and promptly.  Other duties relating to departmental mission, not specifically detailed in this section may be assigned. 

Qualifications / Skills:
  • Advanced technical writing skills and the ability to communicate effectively with peers, department management, and cross-functional coworkers. 
  • Fluent in written English. 
  • Familiarity with compliance requirements within cGMP with an emphasis on method validation and reporting requirements preferred. 
  • Demonstrated excellence in advanced word processing using Microsoft Word. 
  • Demonstrated computer literacy, including spreadsheets, structural drawings, databases, and communication packages preferably in a Windows environment. 
  • Ability to work in a highly independent and self-directed work environment. 
Education, Experience, and Licensing Requirements: (Text Only)- Bachelor's degree in Chemistry or closely related field required.  - Minimum of 2 or more years of experience in a cGMP regulated laboratory environment highly preferred.   Employment Type: FULL_TIME

What Cambrex employees say

Pay

Benefits

Hours and flexibility

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About Cambrex

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

East Rutherford, NJ, US

Year founded

1981

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