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Technical Write Jobs in Michigan (NOW HIRING)

MMS

Nonclinical Writer

Canton, MI · On-site

This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. Roles and Responsibilities: * Strong ...

MMS Holdings Inc.

Nonclinical Writer

Canton, MI · On-site

This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. Roles and Responsibilities: * Strong ...

The Mathworks

Senior Technical Consultant

Novi, MI · On-site

$128K - $199K/yr

Lead AUTOSAR consulting engagements with and deliver technical services to customers. Collaborate with account teams to articulate the value of model-based design and build tools adoption and ...

The C2 Group

Technical Lead

Grand Rapids, MI · On-site +1

The Technical Lead leads complex technical problem solving and owns the most challenging ... This role is ideal for someone who has hands-on experience building AI-enabled workflows, writing ...

The C2 Group

Technical Lead

Grand Rapids, MI

This role is ideal for someone who has hands-on experience building AI-enabled workflows, writing ... Technical Advisor - You're the bridge between big-picture strategy and ground-level execution.

The C2 Group

Technical Lead

Grand Rapids, MI · On-site

$100 - $130/hr

Designing intelligent workflows, writing agents, and finding the right spots to apply automation ... Technical Lead Job Accountabilities Own Technical Processes * Define and maintain the technical ...

JRD Systems

Technical Business Analyst

Dearborn, MI · On-site

Write and optimize SQL queries (3+ years of experience) to investigate data issues, validate ... Create clear, detailed technical documentation, incident reports, and status updates for both ...

Genetec

Technical Trainer

Detroit, MI

$32.25 - $42.75/hr

Proficient verbal and written communication in English, additional languages an asset Technical requirements: * Excellent knowledge of Windows operating systems and virtual machines * Excellent ...

DATAMAXIS, Inc

Technical Business Analyst

Dearborn, MI · On-site

Write, optimize, and troubleshoot SQL queries to: * Investigate production issues. * Validate data accuracy. * Support business and technical analysis. * Work within cloud-based data platforms such ...

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Technical Write information

What jobs can technical writers do?

Technical writers can work in industries such as technology, healthcare, engineering, and manufacturing, creating user manuals, technical documentation, training materials, and online help systems. They often collaborate with subject matter experts and use tools like Adobe FrameMaker, MadCap Flare, or Microsoft Word, and may require certifications in technical communication or related fields.

What is the work of a technical writer?

A technical writer creates clear and concise documentation such as user manuals, guides, and technical reports to help users understand complex information. They often collaborate with engineers and subject matter experts and use tools like Markdown or Adobe FrameMaker to produce accurate materials. Strong writing skills and knowledge of technical concepts are essential for this role.

Are technical writers still in demand?

Technical writers are still in demand across various industries, especially in technology, healthcare, and engineering, as companies need clear documentation for products and services. The role often requires proficiency with tools like Markdown, XML, or content management systems, and demand is expected to grow with increasing technological complexity.
What cities in Michigan are hiring for Technical Write jobs? Cities in Michigan with the most Technical Write job openings:
Technical Write jobs near you
Infographic showing various Technical Write job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 8% Part Time, 1% Temporary, 5% Contract, and 1% Nights. Highlights an 88% Physical, 5% Hybrid, and 7% Remote job distribution.

Nonclinical Writer

MMS

Canton, MI • On-site

Full-time

Re-posted 13 days ago

Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
 
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. 
Roles and Responsibilities:
  • Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator’s Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs)
  • Lead projects independently with minimal oversight, lead the writing (structure, content and messaging) of nonclinical documents, ensure the nonclinical package aligns with current regulatory guidelines and meets scientific integrity
  • Ability to author based on highly technical sources such as GLP and non-GLP nonclinical study reports, in vivo and in vitro nonclinical data
  • Ability to develop a mapping plan for the placement of nonclinical studies within structure of Module 2.4 and 2.6 eCTD submission documents
  • Interpret and analyze applicable pharmacokinetics, pharmacology, and toxicology data (eg, Prism files, bioanalytical reports, clinical pathology reports, PK/TK evaluation reports)
  • Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC
  • Demonstrated ability to lead others to complete complex projects
  • Ability to complete documents according to sponsor’s format, processes, and according to regulatory guidelines
  • Ability to effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment
  • Organizational expert within the nonclinical subject area
  • Excellent written/oral communication and strong time and project management skills
  • Ability to attend regular team meetings, lead client meeting and CRMs
  • Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars
  • Strong understanding of regulatory guidances as it applies to nonclinical submission documents and drug development (eg, ICH, FDA and EMA regulations and guidelines, GLP, GCP, GMP and GDP)
Requirements:
  • BS + in pharmacology, toxicology, biology or chemistry, or related field, with industry experience within regulatory writing, regulatory affairs, laboratory sciences, quality assurance/control
  • Knowledge of GLP, ICH guidelines, and applicable regulatory requirements
  • 2+ years of pharmaceutical regulatory nonclinical writing experience
  • Strong writing and analytical skills
  • Proficiency with MS Office applications.   
  • Hands-on experience with clinical trial and pharmaceutical development preferred
  • Basic understanding of CROs and scientific & nonclinical data/terminology, & the drug development process

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About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980

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