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Manufacturing Process Engineer Jobs in Boston, MA

Enjet Aero, Llc

Manufacturing & Process Engineer

Malden, MA · On-site

$76K - $102K/yr

Manufacturing & Process Engineer Full-time Regular Malden, MA, US 2 days ago Requisition ID: 2075 Enjet Aero machines and fabricates complex jet engine parts, components and assemblies for leading ...

Enjet Aero, LLC

Manufacturing & Process Engineer

Malden, MA · On-site

$76K - $102K/yr

The Manufacturing & Process Engineer is responsible for determining methodology and designs behind producing parts, writing code for CNC machines, as well as creating blueprints and set-up sheets for ...

Boyd

Senior Manufacturing Process Engineer

Woburn, MA · On-site

$113K - $147K/yr

Boyd Thermal by Eaton is seeking a Senior Manufacturing Process Engineer at our Woburn, MA facility. Boyd Corporation, a prominent aerospace and defense component manufacturing company, is renowned ...

Boydcorp

Senior Manufacturing Process Engineer

Woburn, MA

$113K - $147K/yr

Boyd Thermal by Eaton is seeking a Senior Manufacturing Process Engineer at our Woburn, MA facility. Boyd Corporation, a prominent aerospace and defense component manufacturing company, is renowned ...

Affinity Recruiting

Sr. Process Engineer

Norwood, MA · Hybrid

$117K - $152K/yr

Affinity recruiting is working on an exciting new opportunity for an amazing manufacturer in the Norwood, MA location. We are looking for a Thick Film Sr Process Engineer! Competitive pay with an ...

FIBA Technologies, Inc.

Process Engineer

Littleton, MA · On-site

Process Engineer - Manufacturing Automation Position Summary The Process Engineer - Manufacturing Automation is responsible for developing, maintaining, troubleshooting, and improving automated ...

FIBA Technologies, Inc.

Process Engineer

Littleton, MA · On-site

Process Engineer - Manufacturing Automation Position Summary The Process Engineer - Manufacturing Automation is responsible for developing, maintaining, troubleshooting, and improving automated ...

FIBA Technologies, Inc.

Process Engineer

Littleton, MA · On-site

Process Engineer - Manufacturing Automation Position Summary The Process Engineer - Manufacturing Automation is responsible for developing, maintaining, troubleshooting, and improving automated ...

Syner-G

Process Engineer

Plainville, MA · On-site

Support manufacturing readiness activities and process implementation at receiving sites. * Develop detailed process descriptions, process flow diagrams (PFDs), process maps, and supporting technical ...

Syner-G

Process Engineer

Plainville, MA · On-site

Support manufacturing readiness activities and process implementation at receiving sites. * Develop detailed process descriptions, process flow diagrams (PFDs), process maps, and supporting technical ...

Syner-G

Process Engineer

Plainville, MA

Support manufacturing readiness activities and process implementation at receiving sites. * Develop detailed process descriptions, process flow diagrams (PFDs), process maps, and supporting technical ...

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All JobsManufacturing Process Engineer JobsManufacturing Process Engineer Jobs in Boston, MA

Manufacturing Process Engineer information

See Boston, MA salary details

$54.9K

$95.8K

$138K

How much do manufacturing process engineer jobs pay per year?

As of Sep 14, 2026, the average yearly pay for manufacturing process engineer in Boston, MA is $95,814.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,800.00 and $106,500.00 per year, depending on experience, location, and employer.

What does a manufacturing process engineer do?

A Manufacturing Process Engineer is responsible for designing, implementing, and optimizing manufacturing processes within a production facility. Their main goal is to improve efficiency, reduce costs, and ensure product quality by analyzing workflows, selecting appropriate equipment, and troubleshooting production issues. They often collaborate with other engineers, quality assurance teams, and production staff to develop and refine processes. This role may also involve implementing automation, maintaining safety standards, and supporting continuous improvement initiatives.

What are the key skills and qualifications needed to thrive as a manufacturing process engineer?

To thrive as a Manufacturing Process Engineer, you need a solid background in engineering principles, process optimization, and quality control, usually supported by a degree in mechanical, industrial, or manufacturing engineering. Familiarity with CAD software, statistical process control (SPC) tools, Lean/Six Sigma methodologies, and enterprise resource planning (ERP) systems is typically required. Strong problem-solving abilities, analytical thinking, and effective communication skills help distinguish top performers in this role. These skills and qualifications are crucial for improving efficiency, ensuring product quality, and driving continuous improvement in manufacturing operations.

What are some common challenges faced by manufacturing process engineers in optimizing production lines?

Manufacturing Process Engineers often encounter challenges such as balancing efficiency with product quality, integrating new technologies without disrupting ongoing operations, and troubleshooting bottlenecks in the production line. They must work closely with cross-functional teams—including quality assurance, maintenance, and operations—to identify root causes of inefficiencies and implement sustainable solutions. Adapting to evolving industry standards and continuous improvement initiatives is also a key part of the role, requiring flexibility and strong problem-solving skills.

What is the difference between Manufacturing Process Engineer vs Manufacturing Engineer?

AspectManufacturing Process EngineerManufacturing Engineer
Primary FocusDesigning, analyzing, and improving manufacturing processesOverseeing overall manufacturing operations and production workflows
Typical ResponsibilitiesProcess optimization, troubleshooting, implementing new technologiesProduction planning, equipment management, quality control
CredentialsBachelor's in engineering, certifications like Six Sigma often preferredBachelor's in engineering or manufacturing, similar certifications
Work EnvironmentFactories, labs, process development settingsFactories, production lines, plant management

While both roles require engineering backgrounds and similar certifications, Manufacturing Process Engineers focus on refining manufacturing processes, whereas Manufacturing Engineers oversee the entire production process. Understanding these distinctions helps in choosing the right career path or job search focus.

Do manufacturing process engineers make a lot of money?

Manufacturing process engineers typically earn competitive salaries that vary by industry, experience, and location. According to industry data, the median annual salary for this role is often above the national average for engineering positions, with higher earnings possible for those with specialized skills or certifications. They also benefit from opportunities for advancement and overtime in manufacturing environments.
Manufacturing Process Engineer jobs near you
Infographic showing various Manufacturing Process Engineer job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 3% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $95,814 per year, or $46.1 per hour.

Manufacturing Process Engineer

Lexington, MA

Piramal Pharma Limited
See more jobs at Piramal Pharma Limitedexternal

$82K - $110K/yr

Full-time

Re-posted 17 days ago

Key responsibilities

  • Designs, project manages, and implements changes, improvements, new systems, and equipment in the manufacturing process.

  • Supports day-to-day production and maintenance activities, including troubleshooting and maintaining systems and equipment.

  • Develops and modifies SOPs, participates in deviation investigations, and manages technical documentation related to manufacturing systems.

Job description

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Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Manufacturing Process Engineer

Job Description

Business: Pharma Solutions Department: Facilities, Maintenance & Engineering Location: LexingtonJob DescriptionBusiness: Pharma Solutions Department: Facilities, Maintenance & Engineering Location: Lexington Job Overview Reporting to the Engineering Manager, the Manufacturing Process Engineer serves as subject-matter-expert and provides real-time, process engineering support to the manufacturing process. This position is responsible for design, project management, and implementation of new and existing systems, utilities and equipment, and ensures Quality, Compliance, and improved OTIF for all products produced at the manufacturing facility in Lexington, Kentucky. Reporting Structure This position reports to the Engineering Manager. Key Responsibilities: Designs and project manages changes, improvements, new systems and or equipment. Prepares Change Control Records (CCRs), Design Specifications, User Requirements Specifications, System Specifications, Design documents, Drawings, and Validation Documents for improvement, planned and corrective maintenance and system or process improvements Leads/assists in Continuous Improvement Projects, including identification of opportunities, researches literature and vendors, prepares and presents proposals, develops and executes projects, and closes projects, all following appropriate change control methodologies Represents Technical Subject Matter Expert (SME) in teams assembled to specify, install, troubleshoot and maintain systems, equipment and processes Supports day-to-day production and maintenance activities Provides training support as required. Develops and or modifies SOPs for the Processes and Equipment. Participates in deviation investigations to identify root causes and define corrective and preventive actions (CA/PA). Creates and maintains drawings and sketches. Manages Technical Publications Library to ensure the relevant manuals, specifications, design information for all of our facilities, utilities, equipment and products are on hand Primary/First Line responsibility for operation and maintenance of the Validated Systems to maintain production capability required. Primary/First Line responsibility for enhancements and upgrades of manufacturing related systems to maintain production capability. Qualifications: Bachelor's degree in Mechanical, Electrical, or Chemical Engineering Minimum 3-5 years of pharmaceutical manufacturing/maintenance experience required (parenteral/sterile filling experience preferred) Expertise in troubleshooting production equipment/systems Ability to work flexible schedule to support 24-hour operation (requires assignment on shift for 4 shift rotating days off schedule) PC literate with standard office application (Word, Excel, PowerPoint) competency Experience with maintenance and administration of both Windows-based and industrial (e.g., PLC) computer networks. Experience with Allen-Bradley ControlLogix and Siemens PLCs; experience with HMI software applications; experience with automating processes and equipment Knowledge and understanding of cGMPs including FDA, PMDA, and EU regulations; knowledge of cGMP validation requirements and techniques; experience with commissioning and validation protocol development and execution. Knowledge and experience in cGMP CA/PA, root-cause analysis, risk assessment and investigation tools and techniques.

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