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Gmp Jobs in Seattle, WA (NOW HIRING)

Evotec

IT Specialist III, GMP Systems

Redmond, WA · On-site

They are seeking an IT Specialist III to drive impactful projects and support GMP systems in a manufacturing environment, ensuring compliance and effective troubleshooting of IT systems. ...

Evotecgroup

IT Specialist III, GMP Systems

Redmond, WA · On-site

$115K - $126K/yr

Job Title: IT Specialist III, GMP Systems Department: Information Systems Location: Redmond, WA Reports to: Senior IT End User Services Manager About Us: At Just-Evotec, we believe that curiosity is ...

Evotec

IT Specialist III, GMP Systems

Redmond, WA · On-site

$115K - $126K/yr

Job Title: IT Specialist III, GMP Systems Department: Information Systems Location: Redmond, WA Reports to: Senior IT End User Services Manager About Us: At Just-Evotec, we believe that curiosity is ...

Evotec

IT Specialist III, GMP Systems

Redmond, WA · On-site

$115K - $126K/yr

Job Title: IT Specialist III, GMP Systems Department: Information Systems Location: Redmond, WA Reports to: Senior IT End User Services Manager About Us: At Just-Evotec, we believe that curiosity is ...

Three Point Solutions

Medical Assembler

Redmond, WA · On-site

$20 - $23/hr

Follow SOPs, GMP, and quality system procedures * Interpret and execute supervisor/lead instructions * Adapt to new processes and product changes * Cross-train across product lines * Assist in ...

Aurion Biotech Inc.

Senior Engineer, MSAT

Seattle, WA · On-site

$140K - $164K/yr

The Senior Engineer serves as a technical and GMP manufacturing SME within assigned process areas and works closely with CDMOs and cross-functional partners to successfully transfer established ...

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Gmp information

See Seattle, WA salary details

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How much do gmp jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for gmp in Seattle, WA is $37.87, according to ZipRecruiter salary data. Most workers in this role earn between $20.24 and $50.62 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 are popular job titles related to Gmp jobs in Seattle, WA?

For Gmp jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Gmp jobs in Seattle, WA look for?

The top searched job categories for Gmp jobs in Seattle, WA are:

Gmp jobs near you
Infographic showing various Gmp job openings in Seattle, WA as of August 2026, with employment types broken down into 85% Full Time, 13% Contract, and 2% Nights. Highlights an 98% In-person, and 2% Remote job distribution, with an average salary of $78,776 per year, or $37.9 per hour.

IT Specialist III, GMP Systems

Evotec

Redmond, WA • On-site

Full-time

Re-posted 20 days ago

Job description

Job Summary:
Evotec is a forward-thinking company that values curiosity and innovation. They are seeking an IT Specialist III to drive impactful projects and support GMP systems in a manufacturing environment, ensuring compliance and effective troubleshooting of IT systems.
Responsibilities:
• Directly responsible for the deployment, support, and troubleshooting of end user devices such as laptops, workstations, printers, tablets, phones, and audio/video services.
• Directly responsible for the configuration, deployment, and support of GMP systems in a manufacturing facility or laboratory environment
• Take over the responsibility as a System Owner for Manufacturing IT Applications and/or QC Analytics systems in a 24x7 Good Manufacturing Practice (GMP) environment.
• Work with the Business Process Owners for the upgrade/patching and changes to the system to ensure GMP compliance.
• Follow Computerized Systems Validation (CSV) process to build out and qualify/validate GxP systems.
• Directly responsible for deployment, as well as authoring IT validation documents such as System Design and Configuration Specifications (SDCS’s) and Installation Qualifications (IQ), Backup Configuration and Restore Protocols, and System Administration Procedures.
• Assist with and provide input as SME and System Owner for other documents in validation process, such as User and/or Functional Requirements, Risk Assessments, Operational Qualification related to software functions, etc.
• Familiar with Quality Change Management software/processes, to document activities during the project and provide impact assessments.
• Experience implementing various IT tools such as windows NTFS permissions, active directory, group policies, etc. to configure systems to meet data integrity and regulatory requirements.
• Contacting vendors as needed for troubleshooting and resolving issues.
• Creation of user accounts in applications as needed following administration procedures.
Qualifications:
Required:
• Bachelor’s Degree or technical institute degree in Computer Science, Information Systems, or science related field; or equivalent work experience.
• 5+ years of experience working within the Biotech or Pharma industry supporting critical Manufacturing Systems.
• Biopharmaceutical or similar Manufacturing domain.
• Experience as a System Owner for validated GxP Systems.
• Familiar with Data Integrity methodologies.
• Experience writing Standard Operating Procedures (SOPs).
• Basic knowledge of Manufacturing Execution Systems, Distributed Control Systems (DeltaV), LIMS, Data Historian, ERP etc.
• Knowledge of Good Manufacturing Practices (GMP), Health Authority practices, 21 CFR Part 11, cGMP Annex 11, Data Integrity principles.
Company:
Evotec is a pharmaceutical and life science company that provides drug discovery and gene therapy solutions. Founded in 1993, the company is headquartered in Hamburg, DEU, with a team of 5001-10000 employees. The company is currently Late Stage.

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