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Writing Jobs in Cambridge, WI (NOW HIRING)

GMP Technical Writer

Madison, WI · On-site

$69 - $96/hr

The ideal candidate will combine strong technical writing skills with pharmaceutical GMP experience and a solid understanding of quality systems and document control. This position requires the ...

GMP Technical Writer

Madison, WI · On-site

$50 - $70/hr

The ideal candidate will combine strong technical writing skills with pharmaceutical GMP experience and a solid understanding of quality systems and document control. This position requires the ...

GMP Technical Writer

Madison, WI · On-site

$50 - $70/hr

The ideal candidate will combine strong technical writing skills with pharmaceutical GMP experience and a solid understanding of quality systems and document control. This position requires the ...

Hourly Wage: $16 - $29 per/hour *The actual hourly rate will equal or exceed the required minimum wage applicable to the job location. Additional compensation includes annual or quarterly performance ...

Hourly Wage: $14 - $27 per/hour *The actual hourly rate will equal or exceed the required minimum wage applicable to the job location. Additional compensation includes annual or quarterly performance ...

Showing results 21-40

Writing information

See Cambridge, WI salary details

$10.3K

$28.1K

How much do writing jobs pay per year?

As of Sep 1, 2026, the average yearly pay for writing in Cambridge, WI is $26,713.00, according to ZipRecruiter salary data. Most workers in this role earn between $25,800.00 and $27,700.00 per year, depending on experience, location, and employer.

What is writing as a profession?

Writing as a profession involves creating content for various purposes, such as articles, books, advertisements, websites, or technical manuals. Professional writers may work as journalists, novelists, copywriters, content creators, or technical writers, among other roles. Successful writers need strong language skills, creativity, and the ability to adapt their style to suit different audiences or industries. Many writers are self-employed or work on a freelance basis, while others are employed by companies, publishing houses, or media organizations.

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

To thrive as a Writer, you need strong command of language, grammar, and storytelling, often supported by a degree in English, communications, or journalism. Familiarity with word processing software, content management systems, and sometimes SEO tools is typically required. Creativity, adaptability, attention to detail, and effective communication make a writer stand out in this field. These skills are crucial for producing engaging, accurate, and audience-appropriate content across various platforms.

What are some common challenges writers face when working with editors, and how can they effectively navigate them?

Writers often encounter challenges such as receiving extensive feedback, reconciling different editorial perspectives, or adapting their style to fit a publication's voice. To navigate these challenges, it's important to approach feedback with an open mind, communicate clearly with editors about any uncertainties, and be willing to revise work as needed. Building a collaborative relationship with editors not only improves the quality of your writing but also helps you grow professionally and adapt to various editorial standards.

What is the difference between Writing vs Copywriting?

AspectWritingCopywriting
Primary FocusCreating various types of content, such as articles, blogs, reportsCreating persuasive content to promote products or services
Skills NeededResearch, storytelling, clarityPersuasion, marketing, concise messaging
Work EnvironmentMedia companies, publishing houses, online platformsAdvertising agencies, marketing departments, freelance
Common CertificationsWriting courses, journalism degreesCopywriting certifications, marketing courses

Writing involves producing a wide range of content for various purposes, focusing on clarity and information. Copywriting specifically aims to craft persuasive messages to drive sales or engagement. While both roles require strong writing skills, copywriters often focus more on marketing strategies, whereas writers may work in journalism, publishing, or content creation.

How can I start online writing jobs?

To start online writing jobs, create a portfolio of writing samples and register on freelance platforms such as Upwork, Fiverr, or Freelancer. Building a strong profile, applying to relevant jobs, and developing skills in areas like SEO or content marketing can increase your chances of securing work.

Is there a high demand for writers?

Writing is a versatile profession with steady demand across industries such as publishing, marketing, and digital media. The growth of online content and remote work opportunities has increased the need for skilled writers, especially those proficient in SEO, copywriting, and content creation tools.

What jobs can I do if I like writing?

Jobs for those who enjoy writing include content writer, copywriter, technical writer, journalist, editor, and social media manager. These roles often require strong communication skills, proficiency with writing tools, and the ability to meet deadlines in various work environments.

What cities near Cambridge, WI are hiring for Writing jobs?

Cities near Cambridge, WI with the most Writing job openings:

Infographic showing various Writing job openings in Cambridge, WI as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 22% Part Time, and 5% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $26,713 per year, or $12.8 per hour.

GMP Technical Writer

Automated Systems, Inc.

Madison, WI • On-site

$69 - $96/hr

Other

Posted 12 days ago


Job description

Automated Systems, Inc. | Contract to Hire

GMP Technical Writer

Madison, United States | Posted on 08/20/2026

  • Industry Pharma/Biotech/Clinical Research
  • Salary $50 - $70 hourly
  • State/Province Wisconsin
  • City Madison
  • Country United States
Job Description

GMP Technical Writer

Contract: 6+ months with strong potential for contract-to-hire
Location: Greater Madison Area, WI — Onsite

Automated Systems, Inc. (ASI) is seeking an experienced GMP Technical Writer to support documentation and quality system activities at a pharmaceutical manufacturing site in the Greater Madison Area. This role will support backlog closure across Deviations, CAPAs, Change Controls, SOPs, and engineering documentation, working closely with Automation, Utilities, and Facilities engineering teams.

The ideal candidate will combine strong technical writing skills with pharmaceutical GMP experience and a solid understanding of quality systems and document control. This position requires the ability to gather complex technical information from engineers and translate it into clear, accurate, compliant, and audit-ready documentation.

KeyResponsibilities

  • Author, revise, and finalize GMP documentation, including Deviation reports, CAPAs, Change Controls, engineering workorders, SOPs, and Work Instructions.
  • Partner with Automation, Utilities, and Facilities engineers to gather technical information and translate engineering concepts into clear, GMP-compliant documentation.
  • Support Deviation investigations, root cause documentation, corrective and preventive actions, and Change Control packages, including classification and rationale.
  • Manage document workflows through Veeva Quality Docs, MasterControl, or comparable electronic quality management systems, including review, approval, and effective-date processes.
  • Author and edit SOPs, Work Instructions, engineering procedures, and related controlled documents in accordance with site and global quality requirements.
  • Maintain documentation trackers using Smartsheet, Excel, or similar tools to monitor open items, approval queues, dependencies, and closure timelines.
  • Coordinate document interdependencies across engineering and quality functions to prevent routing delays and support timely closure of documentation backlogs.
  • Ensure documentation meets cGMP, data integrity, document control, version control, and audit-readiness requirements.
  • Apply strong attention to detail and critical thinking when reviewing technical content for accuracy, completeness, consistency, and compliance.
Requirements

RequiredQualifications & Experience

  • 4+ years of GMP technical writing experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
  • Demonstrated experience authoring Deviations, CAPAs, Change Controls, SOPs, Work Instructions, and other GMP-controlled documentation.
  • Experience supporting Deviation investigations and CAPA processes, including documenting root causes, corrective actions, and preventive actions.
  • Strong understanding of cGMP documentation practices, data integrity, document control, version control, and review/approval workflows.
  • Experience with electronic quality management or document management systems such as Veeva Quality Docs, MasterControl, TrackWise, or equivalent platforms.
  • Experience using Smartsheet, Microsoft Excel, and Microsoft Office for documentation tracking and project coordination.
  • Relevant experience supporting engineering organizations, particularly Automation, Utilities, Facilities, Manufacturing, or related technical functions.
  • Strong technical writing and editing skills, with the ability to translate complex technical information into clear, concise, compliant, and audit-ready documentation.
  • Excellent attention to detail, organization, critical thinking, and problem-solving skills.
  • Ability to work effectively with engineers, Quality, Operations, and other cross-functional stakeholders in a fast-paced pharmaceutical manufacturing environment.
  • Bachelor’s degree in a relevant discipline such as Technical Writing, Engineering, Science, Business, Computer Science, or a related field, or equivalent combination of education and experience.

PreferredQualifications

  • 2+ years of pharmaceutical industry experience in a GMP-regulated environment.
  • Experience authoring or maintaining electronic batch record recipes.
  • Familiarity with systems such as ComplianceWire, JD Edwards, Unicorn, or similar pharmaceutical quality/manufacturing platforms.
  • Working knowledge of manufacturing and laboratory operations and the ability to quickly learn new processes, systems, and technologies.
  • Experience supporting quality system backlog reduction, documentation remediation, or continuous improvement initiatives.
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