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Gmp Jobs in Madison, WI (NOW HIRING)

Automated Systems, Inc.

GMP Technical Writer

Madison, WI · On-site

$69 - $96/hr

Country United States 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 ...

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: Greater Madison Area, WI -- Onsite Automated Systems, Inc. (ASI) is seeking an experienced GMP Technical ...

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: Greater Madison Area, WI - Onsite Automated Systems, Inc. (ASI) is seeking an experienced GMP Technical ...

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Gmp information

See Madison, WI salary details

$14

$33

$47

How much do gmp jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for gmp in Madison, WI is $33.54, according to ZipRecruiter salary data. Most workers in this role earn between $17.93 and $44.81 per hour, depending on experience, location, and employer.

What is a Gmp?

A GMP (Good Manufacturing Practice) job typically involves ensuring that products, especially in industries like pharmaceuticals, biotechnology, and food production, are consistently produced and controlled according to quality standards. Employees in GMP roles follow strict guidelines to maintain safety, hygiene, and compliance with regulatory requirements. Common GMP job positions include quality control specialists, manufacturing technicians, and regulatory compliance officers.

What are the typical daily responsibilities of a Gmp specialist in a manufacturing facility?

As a GMP specialist, your day may involve overseeing production processes to ensure compliance with regulatory standards, conducting regular audits, and maintaining detailed documentation of all manufacturing activities. You will likely work closely with quality assurance, production, and engineering teams to identify and rectify any deviations from established protocols. Additionally, you may be responsible for training staff on GMP procedures and supporting investigations into product quality issues. This role requires a proactive approach to problem-solving, a keen eye for detail, and frequent interaction with various departments to maintain product quality and safety.

What are the key skills and qualifications needed to thrive in the Gmp position, and why are they important?

To excel in a GMP (Good Manufacturing Practices) specialist role, individuals typically need a strong background in life sciences, quality control, and regulatory compliance, often requiring a relevant bachelor's degree or industry experience. Familiarity with quality management systems, documentation software, and industry-specific certifications like GMP or Six Sigma is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this position. These competencies ensure strict adherence to regulatory standards, product safety, and continuous improvement within pharmaceutical or food manufacturing environments.

Are GMP jobs in demand?

GMP (Good Manufacturing Practice) jobs are in demand in the pharmaceutical, biotech, and food manufacturing industries due to strict regulatory requirements. These roles often require knowledge of quality control, compliance, and relevant certifications, and employment opportunities tend to grow with industry expansion and regulatory updates.

What are typical GMP job duties?

GMP (Good Manufacturing Practice) jobs typically involve ensuring manufacturing processes comply with quality standards, including monitoring production, maintaining documentation, and inspecting facilities. Employees may also be responsible for cleaning, equipment calibration, and adhering to safety protocols, often requiring attention to detail and knowledge of regulatory requirements. These roles are common in pharmaceutical, biotech, and food manufacturing environments.

What is a typical day in a GMP job?

A GMP (Good Manufacturing Practice) job typically involves following strict protocols to ensure product quality and safety, including inspecting manufacturing processes, documenting procedures, and maintaining cleanliness in the production environment. Employees often work in shifts, use specialized equipment, and adhere to regulatory standards set by authorities like the FDA. Attention to detail and compliance with safety guidelines are essential components of daily tasks.

What skills are needed for Gmp jobs?

GMP (Good Manufacturing Practice) jobs require strong attention to detail, knowledge of regulatory standards, and good documentation skills. Familiarity with manufacturing processes, quality control, and relevant certifications such as GMP training or quality assurance are also important. Effective communication and the ability to work in a regulated environment are essential for success in GMP roles.

What job categories do people searching Gmp jobs in Madison, WI look for?

The top searched job categories for Gmp jobs in Madison, WI are:

What cities near Madison, WI are hiring for Gmp jobs?

Cities near Madison, WI with the most Gmp job openings:

Gmp jobs near you
Infographic showing various Gmp job openings in Madison, WI as of August 2026, with employment types broken down into 84% Full Time, 5% Part Time, 6% Contract, and 5% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $69,750 per year, or $33.5 per hour.

GMP Technical Writer

Automated Systems, Inc.

Madison, WI • On-site

$69 - $96/hr

Other

Posted 9 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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