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Medical Writer Jobs in Wisconsin (NOW HIRING)

Description Overview The Technical Writer supports documentation creation and revision activities ... Experience working in FDA-regulated, cGMP, pharmaceutical, nutrition, medical device, food ...

We are looking for a Service Writer to join our team! The right candidate will have automotive service advisor experience and a valid driver's license. The day-to-day duties of this role include ...

We are looking for a Service Writer to join our team! The right candidate will have automotive service advisor experience and a valid driver's license. The day-to-day duties of this role include ...

Technical Writer

Manitowoc, WI · On-site

$61K - $113K/yr

We have an opportunity for a Technical Writer to join our Manitowoc, WI team. You will support the global Product Line by producing high-quality technical documentation appropriate for its intended ...

We have an opportunity for a Technical Writer to join our Manitowoc, WI team. You will support the global Product Line by producing high-quality technical documentation appropriate for its intended ...

Job Title: Technical Writer, Manufacturing Location: Cudahy, WI Type: Long-term Contract ... medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as ...

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GMP Technical Writer

Madison, WI · On-site

$50 - $70/hr

Required Qualifications & Experience * 4+ years of GMP technical writing experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments. * Demonstrated ...

New

The writer coordinates the specifications with drawings and design documents to establish material and installation requirements. The individual also helps create and maintain office standard ...

Showing results 41-60

Medical Writer information

See Wisconsin salary details

$11

$46

$79

How much do medical writer jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for medical writer in Wisconsin is $46.70, according to ZipRecruiter salary data. Most workers in this role earn between $33.99 and $56.54 per hour, depending on experience, location, and employer.

What is a medical writer?

Medical writers are professionals who create scientific documents related to healthcare, medicine, and the life sciences. They produce materials such as clinical study reports, journal articles, regulatory submissions, and educational content for healthcare professionals or the public. Medical writers must have a strong understanding of medical terminology, research methods, and regulatory guidelines. Their work helps communicate complex scientific information clearly, accurately, and in compliance with industry standards.

What does a medical writer do?

Medical writers create scientific documents and articles. This can include a variety of different types of papers, including research documents, educational or promotional literature, articles, and abstracts. You may ghostwrite for well-known physicians and scientists, or you may write under your own name, depending on what field you are in. Other medical writer jobs include journalists for medical magazines, authors of books, and those who write marketing materials for health care organizations. Regardless of your specialty, you must be able to interpret complex scientific information and create articles that people can read and understand, particularly when writing for the general public.

What skills and qualifications are needed to be a medical writer?

To thrive as a Medical Writer, you need a strong background in life sciences or medicine, excellent written communication skills, and often an advanced degree such as a PhD, MD, or relevant certification. Familiarity with reference management software, medical literature databases, and regulatory guidelines like ICH or GPP is typically required. Attention to detail, the ability to interpret complex data, and collaboration skills set standout professionals apart in this role. These competencies ensure the production of accurate, compliant, and accessible medical documents crucial for regulatory approval, education, and communication in healthcare.

How does a medical writer typically collaborate with subject matter experts during a project?

Medical Writers frequently work closely with physicians, researchers, and regulatory specialists to ensure content accuracy and clarity. This collaboration often involves conducting interviews, reviewing scientific data, and incorporating expert feedback into drafts. Building strong professional relationships and maintaining clear communication are key for efficiently resolving technical questions and aligning final documents with project objectives. This teamwork is essential for producing high-quality, compliant materials that meet both scientific and regulatory standards.

What is the difference between Medical Writer vs Clinical Writer?

AspectMedical WriterClinical Writer
CredentialsTypically requires a degree in life sciences, healthcare, or related fields; certifications like AMWA or EMWA are commonSimilar credentials; often holds degrees in life sciences with certifications in clinical research or writing
Work EnvironmentWorks in pharmaceutical, biotech, or healthcare companies, often in offices or remote settingsPrimarily in clinical research organizations, pharmaceutical companies, or hospitals, often in office or remote settings
Industry UsageUsed across pharma, biotech, medical device industries for regulatory, educational, and promotional contentFocused on clinical trial documentation, protocols, and reports within clinical research

Medical Writers and Clinical Writers share similar backgrounds and work environments, often collaborating in healthcare and pharmaceutical sectors. The main difference lies in their focus: Medical Writers create a broad range of medical content, while Clinical Writers specialize in clinical trial documentation and reports.

Do medical writers make good money?

Medical writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced professionals can earn over $100,000, especially with specialized knowledge or certifications. The role often requires strong writing skills and familiarity with scientific or medical terminology.

What are the most commonly searched types of Medical Writer jobs in Wisconsin?

The most popular types of Medical Writer jobs in Wisconsin are:

What are popular job titles related to Medical Writer jobs in Wisconsin?

For Medical Writer jobs in Wisconsin, the most frequently searched job titles are:

What cities in Wisconsin are hiring for Medical Writer jobs?

Cities in Wisconsin with the most Medical Writer job openings:

What are popular job titles related to Medical Writer jobs in WI?

For Medical Writer jobs in WI, the most frequently searched job titles are:

Infographic showing various Medical Writer job openings in Wisconsin as of August 2026, with employment types broken down into 76% Full Time, 8% Part Time, 8% Contract, and 8% Nights. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $97,135 per year, or $46.7 per hour.

Technical Writer

Perrigo

Eau Claire, WI • On-site

Full-time

Posted 18 days ago


Perrigo rating

8.5

Company rating: 8.5 out of 10

Based on 56 frontline employees who took The Breakroom Quiz

18th of 86 rated pharmaceutical


Job description

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.

Join us on our One Perrigo journey as we evolve to win in self-care.

Description Overview

The Technical Writer supports documentation creation and revision activities related to production processes, equipment operation, cleaning, testing, forms, logs, attachments, checklists, and other controlled documents.

The role goes beyond document production by assessing the training and capability impact of changes, capturing critical operational knowledge, improving usability of instructions, and supporting effective implementation of process changes.

This position works closely with cross-functional partners to ensure documentation is accurate, compliant, easy to follow, aligned with root cause and CAPA needs, and effective for the employees who perform the work.

Scope of the Role

Controlled Documentation & Technical Writing
•    Recommend, draft, revise, and maintain SOPs, standard work instructions, work aids, logs, forms, attachments, checklists, and other controlled documentation.
•    Prepare clear written descriptions of work processes using approved formats, templates, and style expectations.
•    Fulfill requests from the document change request process and clearly communicate barriers, resource needs, and timeline risks.
•    Ensure document content meets applicable quality, compliance, operational, and site requirements.
Training Impact & Change Implementation
•    Evaluate documentation changes to determine whether training, retraining, communication, or performance support is required.
•    Identify affected roles, departments, and employee populations impacted by procedural or process changes.
•    Partner with Training & Development, Master Trainers, Quality, Engineering, and Operations to support effective change implementation.
•    Support readiness planning for engineering changes, continuous improvement projects, CAPAs, new equipment, and procedural updates.
SME Interviewing, Knowledge Capture & Standardization
•    Interview and facilitate discussions with subject matter experts to understand current work processes, critical steps, decision points, common errors, and process gaps.
•    Capture tacit and tribal knowledge from experienced employees and translate it into standardized, usable documentation and learning resources.
•    Support development of knowledge repositories, visual references, job aids, and standardized resources that improve consistency across teams or sites.
•    Identify inconsistencies, ambiguity, or missing information in existing procedures and collaborate with SMEs to resolve gaps.
Human Performance, Usability & Visual Communication
•    Improve documentation usability by reducing unnecessary complexity, clarifying critical steps, and applying human performance improvement principles.
•    Develop visual work instructions, process maps, flowcharts, equipment annotations, job aids, photographs, and other visual supports as appropriate.
•    Consider how operators learn and execute work, including likely error points, task sequence, critical controls, and opportunities for visual or point-of-use support.
•    Assess whether documentation is practical, understandable, and effective for the intended users.
CAPA, Root Cause & Continuous Improvement Support
•    Participate in technical writer, continuous improvement, and CAPA-related meetings to understand priorities, scope of work, and rationale for procedural changes.
•    Contribute to CAPA-related projects by ensuring documentation changes align with the root cause and intended corrective or preventive action.
•    Use basic understanding of deviations, investigations, risk assessments, and process performance indicators to understand why procedures are changing.
•    Support continuous improvement by identifying document-related barriers that could contribute to errors, deviations, rework, or inconsistent execution.
Digital Learning & Content Enablement
•    Support development of digital job aids, micro-learning resources, LMS-supporting content, and electronic performance support materials when appropriate.
•    Use approved technology and AI-assisted content tools responsibly to improve drafting, version comparison, SME interview summaries, consistency, and productivity.
•    Measure and improve documentation effectiveness by gathering feedback, reviewing usability, and considering whether updates improve execution, reduce errors, support training effectiveness, or prevent recurrence.

Experience Required
  • Bachelor’s degree in Technical Writing, Communications, Education, Instructional Design, Engineering, Manufacturing, Science, or a related field preferred.
  • Minimum three (3) years of experience in technical writing, manufacturing operations, training, quality systems, or regulated documentation.
  • Experience working in FDA-regulated, cGMP, pharmaceutical, nutrition, medical device, food manufacturing, or similar regulated environments preferred.
  • Proficiency with Microsoft Office applications; ability to learn and utilize document management systems, learning management systems (LMS), and digital content tools.
  • Demonstrated ability to manage multiple priorities, collaborate across functions, gather information from subject matter experts (SMEs), and effectively communicate project needs and challenges.
Preferred Competencies
  • Knowledge of adult learning principles, task analysis, performance-based training, and knowledge transfer methodologies.
  • Experience conducting SME interviews, capturing institutional knowledge, and standardizing documentation across teams and locations.
  • Understanding of quality and process improvement concepts, including CAPA, root cause analysis, risk assessment, process mapping, and workflow documentation.
  • Ability to develop visual and digital learning materials, including work instructions, flowcharts, job aids, equipment annotations, photography, micro-learning content, and LMS-based training.
  • Strong change management skills, including stakeholder engagement, communication planning, implementation support, and continuous improvement practices.
  • Experience leveraging AI and content automation tools to support document creation, content review, version comparison, and standardization efforts.

Benefits
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.

Find out more about Total Rewards at Perrigo.

We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here

Applicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo


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