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Gmp Manufacturing Engineer Jobs (NOW HIRING)

Sharp Services

Manufacturing Engineer

Allentown, PA · On-site

$72K - $92K/yr

Ensure all manufacturing activities comply with Good Manufacturing Practices (GMP), FDA regulations ... Provide engineering support during production to resolve mechanical, electrical, or process-related ...

Sharp Services

Manufacturing Engineer

Allentown, PA · On-site

$72K - $93K/yr

Ensure all manufacturing activities comply with Good Manufacturing Practices (GMP), FDA regulations ... Provide engineering support during production to resolve mechanical, electrical, or process-related ...

The AES Group

Jr. Manufacturing Engineer

Camarillo, CA · On-site

Role: Jr. Manufacturing Engineer Location: Camarillo, CA. Let's create our future together at The ... Experience working within GMP, FDA, and ISO 13485 regulated environments. * Strong understanding of ...

TAE

Manufacturing Engineer

Irvine, CA · On-site

$110K - $140K/yr

Provides technical support for production equipment in a GMP manufacturing environment. About the Role Building and scaling up manufacturing capability. Collaborate with scientists, design engineer ...

Fusion Energy Base

Manufacturing Engineer

Irvine, CA · On-site

$110K - $140K/yr

Provides technical support for production equipment in a GMP manufacturing environment. * Building and scaling up manufacturing capability. * Collaborate with scientists, design engineer, and quality ...

TAE Life Sciences

Manufacturing Engineer

Irvine, CA · On-site

$110K - $140K/yr

Provides technical support for production equipment in a GMP manufacturing environment. About the Role Building and scaling up manufacturing capability. Collaborate with scientists, design engineer ...

System One

Manufacturing Engineer

Cary, IL · On-site

$45 - $51/hr

Develop appropriate supporting documentation, SOPs and work instructions compliant with Good Manufacturing Practices (GMP). * Collaborate with product and manufacturing engineering, equipment vendors ...

System One

Manufacturing Engineer

Cary, IL · On-site

$45 - $51/hr

Develop appropriate supporting documentation, SOPs and work instructions compliant with Good Manufacturing Practices (GMP). * Collaborate with product and manufacturing engineering, equipment vendors ...

System One

Manufacturing Engineer

Cary, IL · On-site

$45 - $51/hr

Develop appropriate supporting documentation, SOPs and work instructions compliant with Good Manufacturing Practices (GMP). * Collaborate with product and manufacturing engineering, equipment vendors ...

System One

Manufacturing Engineer

Cary, IL · On-site

$45 - $51/hr

Develop appropriate supporting documentation, SOPs and work instructions compliant with Good Manufacturing Practices (GMP). * Collaborate with product and manufacturing engineering, equipment vendors ...

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Gmp Manufacturing Engineer information

See salary details

$47.5K

$85.6K

$120K

How much do gmp manufacturing engineer jobs pay per year?

As of Sep 13, 2026, the average yearly pay for gmp manufacturing engineer in the United States is $85,613.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,000.00 and $94,000.00 per year, depending on experience, location, and employer.

What is a GMP manufacturing engineer?

A GMP Manufacturing Engineer is a professional responsible for ensuring that manufacturing processes in industries like pharmaceuticals, biotechnology, and food production comply with Good Manufacturing Practice (GMP) standards. They design, optimize, and monitor production systems to guarantee product quality, safety, and regulatory compliance. Their role often involves troubleshooting equipment, coordinating with quality assurance teams, and implementing process improvements to maintain consistent manufacturing standards.

What are some typical challenges faced by a GMP manufacturing engineer, and how can they be addressed?

GMP Manufacturing Engineers often face challenges related to maintaining strict compliance with regulatory standards, troubleshooting equipment issues, and managing documentation for batch records. Adapting to frequent audits and process changes requires strong attention to detail and effective communication with cross-functional teams such as quality assurance and production. Staying proactive with continuous training and fostering a culture of collaboration can help address these challenges and ensure consistent product quality.

What are the key skills and qualifications needed to thrive as a GMP manufacturing engineer, and why are they important?

To thrive as a GMP Manufacturing Engineer, you need a solid background in engineering principles, process optimization, and regulatory compliance, typically with a degree in engineering or a related field. Familiarity with Good Manufacturing Practices (GMP), validation protocols, and systems like SCADA or MES is crucial, and certifications such as Six Sigma or Lean Manufacturing can be advantageous. Strong problem-solving abilities, attention to detail, and effective communication are vital soft skills in this role. These competencies ensure that manufacturing processes are efficient, compliant, and produce high-quality products in regulated environments.

What is the difference between Gmp Manufacturing Engineer vs Quality Assurance Specialist?

AspectGmp Manufacturing EngineerQuality Assurance Specialist
CredentialsBachelor's in Engineering, GMP trainingBachelor's in Science, GMP/QA certifications
Work EnvironmentManufacturing floors, production linesQuality labs, inspection areas
Industry UsagePharmaceutical, biotech manufacturingPharmaceutical, biotech, medical devices

Gmp Manufacturing Engineers focus on designing, implementing, and maintaining manufacturing processes to ensure GMP compliance. Quality Assurance Specialists primarily monitor and verify product quality through inspections and testing. While both roles require GMP knowledge and collaborate closely, the engineer emphasizes process development, whereas the QA specialist concentrates on quality verification and compliance.

What states have the most Gmp Manufacturing Engineer jobs?

States with the most job openings for Gmp Manufacturing Engineer jobs include:

What are popular job titles related to Gmp Manufacturing Engineer jobs?

For Gmp Manufacturing Engineer jobs, the most frequently searched job titles are:

Infographic showing various Gmp Manufacturing Engineer job openings in the United States as of June 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $85,613 per year, or $41.2 per hour.

Manufacturing Engineer

Allentown, PA • On-site

Sharp Services
See more jobs at Sharp Servicesexternal

$72K - $92K/yr

Full-time

Posted 18 days ago

Job description

Our work truly matters and our resourcefulness can make all the difference in getting life-saving drugs to the people who need them, when they need them. We're more efficient and effective when we're not overly bound to a set way of working. Bring your resourcefulness and agility to continue your career at Sharp.

The Manufacturing Engineer will play a crucial role in the design, optimization, and troubleshooting of manufacturing processes to ensure efficient, safe, and high-quality production of pharmaceutical products. This position requires hands on trouble shooting of electromechanical packaging equipment. This position involves close collaboration with cross-functional teams to support process improvement, compliance with regulatory requirements, and continuous improvement in a highly regulated environment.


Key Responsibilities:
Process Optimization: Design, develop, and implement processes to improve manufacturing efficiency, reduce waste, and enhance product quality. Troubleshoot and resolve production issues to minimize downtime and ensure
smooth operations.
Equipment and Technology Management: Evaluate, select, and oversee the installation and maintenance of manufacturing equipment, ensuring they are functioning according to specifications and industry standards.
Compliance and Documentation: Ensure all manufacturing activities comply with Good Manufacturing Practices (GMP), FDA regulations, and other relevant standards. Maintain accurate records, reports, and documentation in accordance with regulatory guidelines.
Author technical documents such as Change Controls and WRKI's, Review MPR's etc.
Quality Control and Assurance: Collaborate with quality assurance teams to identify and implement corrective actions, conduct root cause analysis for quality issues, and ensure continuous product quality in the production process.
Project Management: Lead or participate in cross-functional teams for process improvement, facility upgrades, or new product introduction projects. Provide technical guidance on new product development and scale-up processes.
Training and Support: Train and mentor operators and technicians on new processes, equipment, and safety procedures to ensure effective and efficient production workflows.

Continuous Improvement: Identify opportunities for process automation, cost reduction, and other performance improvements. Foster a culture of continuous improvement using Lean, Six Sigma, or similar methodologies.
Troubleshooting: Provide engineering support during production to resolve mechanical, electrical, or process-related problems in a timely manner.
Safety and Risk Management: Promote a safe working environment by adhering to health and safety protocols and identifying any potential risks or hazards in the manufacturing processes.

Required Qualifications:
Bachelor's degree in Mechanical Engineering, Chemical Engineering, Pharmaceutical Engineering, or a related field. (Degree in progress will be considered)
3+ years of experience in a manufacturing engineering role, preferably within the pharmaceutical or life sciences industry.
Strong understanding of pharmaceutical manufacturing processes, equipment, and regulatory requirements (FDA, GMP, etc.).
Experience with process design, process control, and equipment validation in a regulated manufacturing environment.
Proficiency in the use of engineering software, such as AutoCAD, SolidWorks, or process simulation tools.
Familiarity with Lean Manufacturing, Six Sigma, or similar continuous improvement methodologies.

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