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$45.5K

$102.9K

$166.5K

How much do pharmaceutical mechanical engineering jobs pay per year?

As of Sep 4, 2026, the average yearly pay for pharmaceutical mechanical engineering in the United States is $102,878.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,500.00 and $126,500.00 per year, depending on experience, location, and employer.

What is pharmaceutical mechanical engineering?

A Pharmaceutical Mechanical Engineering job involves designing, developing, and maintaining mechanical systems used in pharmaceutical manufacturing. Engineers in this field ensure that equipment such as bioreactors, tablet presses, and packaging machines operate efficiently and comply with industry regulations. They work on process optimization, automation, and maintenance to enhance production quality and safety. This role requires expertise in mechanical engineering principles, regulatory standards, and Good Manufacturing Practices (GMP). Additionally, they collaborate with cross-functional teams to improve manufacturing processes and troubleshoot technical issues.

What does a pharmaceutical mechanical engineer do?

As a Pharmaceutical Mechanical Engineer, your daily responsibilities may include designing, maintaining, and optimizing equipment used in pharmaceutical production, conducting equipment validation and troubleshooting, and ensuring compliance with industry regulations such as GMP. You will likely work closely with cross-functional teams, including quality assurance, process engineering, and production staff, to implement process improvements and resolve technical issues. Regular activities also involve preparing technical documentation, participating in audits, and recommending upgrades or modifications to enhance reliability and efficiency. The role often requires a balance between hands-on equipment work and project management tasks.

What skills and qualifications are needed for pharmaceutical mechanical engineering?

To thrive in Pharmaceutical Mechanical Engineering, you need a solid background in mechanical engineering principles, pharmaceutical manufacturing processes, and regulatory compliance, often supported by a degree in mechanical engineering or a related field. Familiarity with computer-aided design (CAD) software, Good Manufacturing Practice (GMP) standards, and equipment validation tools is typically required. Strong problem-solving abilities, teamwork, and communication skills help you effectively address technical challenges and collaborate across multidisciplinary teams. These capabilities are essential to ensuring the safe, efficient, and compliant design and maintenance of pharmaceutical manufacturing systems.

Can a pharmaceutical mechanical engineer work in the pharmaceutical industry?

Yes, a pharmaceutical mechanical engineer can work in the pharmaceutical industry, where they design, maintain, and optimize equipment and facilities used in drug manufacturing and processing. Their skills in HVAC systems, cleanroom environments, and process equipment are highly relevant in this sector.

Do pharmaceutical mechanical engineers make good money?

Pharmaceutical mechanical engineers typically earn competitive salaries due to their specialized skills in designing and maintaining manufacturing equipment for the pharmaceutical industry. Salaries vary based on experience, location, and certifications, but the field generally offers strong compensation and job stability. Advanced knowledge of HVAC systems, cleanroom environments, and regulatory standards can enhance earning potential.

What can I do with a pharmaceutical mechanical engineering degree?

A pharmaceutical mechanical engineering degree prepares individuals to design, develop, and maintain equipment and facilities used in pharmaceutical manufacturing. Graduates can work in areas such as process engineering, equipment design, facility validation, and compliance with industry standards like GMP. Skills in CAD, automation, and regulatory knowledge are often essential for these roles.
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Pharmaceutical Mechanical Engineering jobs near you
Infographic showing various Pharmaceutical Mechanical Engineering job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, 4% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $102,878 per year, or $49.5 per hour.

PHARMACEUTICAL - MECHANICAL UTILITIES ENGINEER

MMR Consulting

Greenville, SC • On-site

Other

Posted 23 days ago

Job description

Previous Pharmaceutical/Biotech experience is mandatory for this role.
MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical /biotechnology and highly regulated industries. Its services include Engineering, Project Management, and Validation.
MMR Consulting has offices across North America and Asia.
This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers involved in the design, commissioning & qualification, start-up and project management of various processes, systems and facilities. The work may require working out of client's facilities, in Raleigh North Carolina.
Responsibilities
  • Provide technical guidance into the design, installation commissioning, qualification, start-up and operations of various pharmaceutical / biopharmaceutical facilities and utilities such as Purified Water (PW), Water For Injection (WFI), Clean Steam (CS), Heating, Ventilation & Air Conditioning (HVAC), Process Compressed Air (CA) & Gases
  • Lead the development of key design, technology selections, engineering and commissioning / qualification deliverables such as PFDs, P&IDs, specifications, equipment and distribution loop layouts, DQ, FAT, Commissioning Test Plans & checklists, IQ, OQ, PQ during the project lifecycle
  • Able to support detailed design development, field installation and perform field execution of commission & qualification test cases and protocols
  • Serve as technical SME on the design and operation aspects of clean utilities. Possess knowledge of regulatory requirements, mechanical specifications and industry best practices and guidelines for clean utilities.
  • Lead the design, procurement, field installation, commissioning and qualification processes throughout the project lifecycle to ensure timely completion and to ensure all quality and engineering specifications are met.
  • Support development of Project Validation Plans (PVPs) to ensure the action plan to test the system is applicable and relevant.
  • Coordinate meetings with cross-functional departments, to drive design reviews, project progress, facilitate decisions, and provide updates.
  • Travel may be occasionally required for meetings with equipment fabrication vendors or Factory Acceptance Testing (FATs).
  • Work may require occasional support over shutdowns or extended hours, specifically during installation, construction, commissioning, qualification and validation phases.
  • Visit construction and installation sites, wearing necessary safety PPE.
  • You may be involved with other aspects such as client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc.
  • Supervise contractors during critical testing of system and equipment.
  • Other duties assigned by client, and/or MMR, based on workload and project requirements.
  • As this position requires working on client sites, you will need to comply with the client's safety rules including mandatory vaccination policies for COVID-19, where applicable

Qualifications
  • 5+ years of experience in commissioning, qualification or validation of various clean utility systems within the pharmaceutical/biotech industry.
  • Previous experience in the pharmaceutical / biotech industry, with knowledge of requirements for cGMP operations.
  • Expertise in generation, storage and distribution of pharmaceutical-grade water systems
  • Hands-on experience with industrial utilities, including:
    • Compressed air generation and distribution
    • Ammonia chillers
    • Electro boilers
    • Chilled water generation and distribution
    • Cooling water generation and distribution
    • Chilled glycol generation and distribution
    • Cooling towers
  • Hands-on experience with clean utilities, including:
    • Purified Water (PW) generation
    • Water For Injection (WFI) generation
    • Clean Steam (CS) generation
  • Hands-on experience with HVAC systems, including:
    • Air handling units (AHUs)
    • Dedicated outdoor air systems (DOAS)
    • Blower coil units
    • Air curtains
    • Computer room air conditioning (CRAC) units
    • DX cooling units
  • Experience with developing and executing validation projects to Risk-Based Commissioning & Qualification approaches, such as ASTM E-2500 or ISPE ICQ, is considered an asset.
  • Experience with commissioning and qualifications of process control systems are considered an asset.
  • Lead teams of staff, manage staff priorities, provide mentorship/oversight, help staff resolve issues. Leadership is considered an asset but not required.
  • Possess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexities.
  • Possess mentorship skills, to coach and develop junior and intermediate employees.
  • Engineering degree, preferably in Mechanical, Electrical or Chemical.
  • Travel may be required on occasion.
  • Ability to handle multiple projects and work in a fast-paced environment.
  • Strong multi-tasking skills

Equal Employment Opportunity and Reasonable Accommodations
MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.

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