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Gmp Engineering Jobs (NOW HIRING)

E Solutions

GMP Engineer

Indianapolis, IN

Work closely with engineering teams, quality assurance, and regulatory personnel. * Collaborate ... Strong understanding of GMP, GAMP, and FDA regulatory standards . * Experience executing IQ, OQ ...

E Solutions

GMP Engineer

Indianapolis, IN · On-site

Work closely with engineering teams, quality assurance, and regulatory personnel. * Collaborate ... Strong understanding of GMP, GAMP, and FDA regulatory standards . * Experience executing IQ, OQ ...

MSD

Specialist, Engineering

Rahway, NJ · On-site

Maintain GMP documentation where applicable, such as GMP engineering drawings and equipment database tracking. Support the mechanical aspects of clinical operations. Coordinate activities executed by ...

Merck & Co., Inc.

Specialist, Engineering

Rahway, NJ · On-site

Maintain GMP documentation where applicable, such as GMP engineering drawings and equipment database tracking. Support the mechanical aspects of clinical operations. Coordinate activities executed by ...

MSD

Associate Specialist, Engineering

Rahway, NJ · On-site

Maintain GMP documentation where applicable, such as GMP engineering drawings and equipment database tracking. Support the mechanical aspects of clinical operations. Coordinate activities executed by ...

Grifols

Plant Maintenance Engineer

Clayton, CA · On-site

... GMP engineering tasks. Additional Skills Needed: * Self-motivated and driven to succeed * Hands-on and a problem solver. Greater time in the field than at the desk. * Communicates effectively and ...

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Gmp Engineering information

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How much do gmp engineering jobs pay per year?

As of Jun 14, 2026, the average yearly pay for gmp engineering in the United States is $137,006.00, according to ZipRecruiter salary data. Most workers in this role earn between $121,500.00 and $151,500.00 per year, depending on experience, location, and employer.

What is the difference between Gmp Engineering vs Quality Assurance Engineer?

AspectGmp EngineeringQuality Assurance Engineer
Required CredentialsEngineering degree, GMP trainingEngineering or science degree, GMP knowledge
Work EnvironmentPharmaceutical manufacturing, labsQuality control labs, production sites
Employer & IndustryPharma companies, biotech firmsPharma, biotech, medical device companies

Gmp Engineering focuses on designing, maintaining, and validating manufacturing processes to ensure compliance with GMP standards. Quality Assurance Engineers oversee product quality, perform audits, and ensure processes meet quality standards. While both roles require GMP knowledge and work within the pharmaceutical industry, Gmp Engineers are more involved in process engineering, whereas QA Engineers focus on quality control and assurance.

What cities are hiring for Gmp Engineering jobs? Cities with the most Gmp Engineering job openings:
Facilities Engineer / Maintenance Engineer

Facilities Engineer / Maintenance Engineer

Intellectt INC

Plainville, MA • On-site

Contractor

Posted 4 days ago

Job description

Job Summary:
We are seeking a Facilities Engineer to support engineering documentation management, CAD services, and spare parts program administration within a regulated pharmaceutical manufacturing environment. The ideal candidate will ensure engineering records, drawings, and documentation remain accurate, compliant, and inspection-ready while supporting facility and utility operations.

Key Responsibilities:
• Serve as the primary liaison between Facilities Engineering, Validation, Quality, and Project Management teams
• Maintain GMP and Non-GMP engineering drawings and documentation
• Manage engineering records through Adept Documentation and CAD systems
• Develop and maintain procedures and periodic review schedules for engineering documentation
• Support change controls, deviations, CAPAs, and documentation implementation activities
• Manage EDMS document routing, review, and approval workflows
• Generate spare parts risk assessments for critical facility, utility, and equipment systems
• Ensure proper inventory controls for spare parts supporting maintenance activities
• Update and maintain engineering-related CMMS work orders
• Support internal audits and regulatory inspections
• Oversee contractor compliance with site documentation standards

Required Qualifications:
• Bachelor's degree in Engineering or related technical field preferred
• 3+ years of engineering documentation or document control experience in a regulated industry
• Experience with Adept CAD and drawing management systems
• Experience with CMMS systems (Blue Mountain preferred)
• Knowledge of GMP documentation requirements and change management processes
• Experience supporting pharmaceutical, biotechnology, or medical device manufacturing environments

Preferred Skills:
• Experience with EDMS workflows
• Familiarity with FDA-regulated environments and CGMP requirements
• Strong organizational, documentation, and communication skills

Recommended Industries:
• Pharmaceuticals
• Biotechnology
• Medical Devices
• Life Sciences Manufacturing
• GMP-Regulated Manufacturing