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Contract Smartsheet Developer Jobs in Wisconsin (NOW HIRING)

ASI Systems Engineering

GMP Technical Writer

Madison, WI · On-site

$50 - $70/hr

GMP Technical Writer Contract: 6+ months with strong potential for contract-to-hire Location ... This position requires the ability to gather complex technical information from engineers and ...

Ryan Companies

Quality Field Engineer

Milwaukee, WI · On-site

... with the established contract documents, in preparation for equipment commissioning ... Track and log all AHJ inspections using Smartsheet Work Apps and ensure all AHJ Inspection ...

Ryan Companies

Quality Field Engineer

Milwaukee, WI · On-site

... with the established contract documents, in preparation for equipment commissioning ... Track and log all AHJ inspections using Smartsheet Work Apps and ensure all AHJ Inspection ...

Automated Systems, Inc.

GMP Technical Writer

Madison, WI · On-site

$80 - $100/hr

Automated Systems, Inc. | Contract to Hire GMP Technical Writer Madison, United States | Posted on ... This position requires the ability to gather complex technical information from engineers and ...

Automated Systems, Inc.

GMP Technical Writer

Madison, WI · On-site

$50 - $70/hr

GMP Technical Writer Contract: 6+ months with strong potential for contract-to-hire Location ... This position requires the ability to gather complex technical information from engineers and ...

Pioneer Metal Finishing

Quality Engineer

Green Bay, WI · On-site

$70K - $90K/yr

Perform contract and feasibility reviews through the First Article, Sample and Quotation Systems ... Strong computer skills; skilled in Excel, Word, PowerPoint, Minitab, Smartsheet. * Excellent ...

Stellar IT Group

Project Manager-Senior

Madison, WI · On-site

Project Manager-Senior Contract: 6 Months Location: Madison, WI Description: * We are currently ... Reporting to the Director of Engineering, the Technical Project Manager will be an engineering ...

E Tech Group

Project Manager

Milwaukee, WI · On-site

We're one of the largest engineering and system integration firms in the United States providing ... Drive Scope - Maintain firm control of scope and compliance with specifications and contract ...

E Tech Group

Project Manager

Port Washington, WI · On-site

We're one of the largest engineering and system integration firms in the United States providing ... Drive Scope - Maintain firm control of scope and compliance with specifications and contract ...

E Tech Group

Project Manager

Port Washington, WI · On-site

We're one of the largest engineering and system integration firms in the United States providing ... Drive Scope - Maintain firm control of scope and compliance with specifications and contract ...

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All JobsContract Smartsheet Developer JobsContract Smartsheet Developer Jobs in Wisconsin

Contract Smartsheet Developer information

What is a Contract Smartsheet Developer?

A Contract Smartsheet Developer is a professional hired on a contractual basis to design, develop, and optimize solutions using Smartsheet, a popular collaborative work management platform. Their responsibilities typically include creating custom workflows, automating processes, and integrating Smartsheet with other systems to meet a company’s unique business needs. They often work remotely or as consultants and may collaborate with project managers, IT teams, or business analysts. Contract Smartsheet Developers must have strong technical skills and a good understanding of project management principles.

What are the key skills and qualifications needed to thrive as a Contract Smartsheet Developer?

To thrive as a Contract Smartsheet Developer, you need expertise in Smartsheet platform features, workflow automation, and data integration, typically backed by experience in business process optimization or a related field. Familiarity with Smartsheet Control Center, DataMesh, and APIs, and certifications like Smartsheet Product Certification are highly valuable. Strong problem-solving, communication, and client management skills set top developers apart in this role. These skills ensure that you can deliver efficient, scalable solutions tailored to client needs while maintaining clear collaboration and project success.

What are the typical challenges a Contract Smartsheet Developer might face when working with diverse client projects?

As a Contract Smartsheet Developer, you may encounter projects with varying requirements, levels of Smartsheet adoption, and client familiarity. A common challenge is quickly understanding unique business processes and translating them into efficient Smartsheet solutions under tight deadlines. Additionally, you might need to integrate Smartsheet with other tools or systems, which requires both technical adaptability and clear communication with client stakeholders. Effective time management and the ability to educate clients on best practices are also key to overcoming these challenges and delivering successful outcomes.

What are popular job titles related to Contract Smartsheet Developer jobs in Wisconsin?

For Contract Smartsheet Developer jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Contract Smartsheet Developer jobs in Wisconsin look for?

The top searched job categories for Contract Smartsheet Developer jobs in Wisconsin are:

What cities in Wisconsin are hiring for Contract Smartsheet Developer jobs?

Cities in Wisconsin with the most Contract Smartsheet Developer job openings:

Contract Smartsheet Developer jobs near you
Infographic showing various Contract Smartsheet Developer job openings in Wisconsin as of August 2026, with employment types broken down into 83% Full Time, 4% Part Time, and 13% Contract. Highlights an 80% Physical, 6% Hybrid, and 14% Remote job distribution.

GMP Technical Writer

ASI Systems Engineering

Madison, WI • On-site

$50 - $70/hr

Contractor

Posted 18 days ago

Key responsibilities

  • Author, revise, and finalize GMP documentation including Deviations, CAPAs, Change Controls, engineering workorders, SOPs, and Work Instructions.

  • Partner with engineering teams to gather technical information and translate engineering concepts into GMP-compliant documentation.

  • Manage document workflows through electronic quality management systems, including review, approval, and closure of documentation backlogs.

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.
Key Responsibilities
  • Author, revise, and finalize GMP documentation,including Deviation reports, CAPAs, Change Controls, engineering workorders, SOPs, and Work Instructions.
  • Partner with Automation, Utilities, and Facilitiesengineers to gather technical information and translate engineeringconcepts into clear, GMP-compliant documentation.
  • Support Deviation investigations, root causedocumentation, corrective and preventive actions, and Change Controlpackages, including classification and rationale.
  • Manage document workflows through VeevaQualityDocs, MasterControl, or comparable electronic quality managementsystems, including review, approval, and effective-date processes.
  • Author and edit SOPs, Work Instructions,engineering procedures, and related controlled documents in accordancewith 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 acrossengineering and quality functions to prevent routing delays and supporttimely closure of documentation backlogs.
  • Ensure documentation meets cGMP, data integrity,document control, version control, and audit-readiness requirements.
  • Apply strong attention to detail and criticalthinking when reviewing technical content for accuracy, completeness,consistency, and compliance.

Requirements
Required Qualifications & Experience
  • 4+ years of GMP technical writing experiencewithin pharmaceutical, biotechnology, medical device, or other regulatedmanufacturing environments.
  • Demonstrated experience authoring Deviations,CAPAs, Change Controls, SOPs, Work Instructions, and other GMP-controlleddocumentation.
  • Experience supporting Deviation investigations andCAPA processes, including documenting root causes, corrective actions, andpreventive actions.
  • Strong understanding of cGMP documentationpractices, data integrity, document control, version control, andreview/approval workflows.
  • Experience with electronic quality management ordocument management systems such as Veeva QualityDocs, MasterControl,TrackWise, or equivalent platforms.
  • Experience using Smartsheet, Microsoft Excel, andMicrosoft Office for documentation tracking and project coordination.
  • Relevant experience supporting engineeringorganizations, particularly Automation, Utilities, Facilities,Manufacturing, or related technical functions.
  • Strong technical writing and editing skills, withthe 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 afast-paced pharmaceutical manufacturing environment.
  • Bachelor's degree in a relevant discipline such asTechnical Writing, Engineering, Science, Business, Computer Science, or arelated field, or equivalent combination of education and experience.

Preferred Qualifications
  • 2+ years of pharmaceutical industry experiencein a GMP-regulated environment.
  • Experience authoring or maintaining electronicbatch record recipes.
  • Familiarity with systems such as ComplianceWire,JD Edwards, Unicorn, or similar pharmaceutical quality/manufacturingplatforms.
  • Working knowledge of manufacturing and laboratoryoperations and the ability to quickly learn new processes, systems, andtechnologies.
  • Experience supporting quality system backlogreduction, documentation remediation, or continuous improvementinitiatives.

Apply