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Process Engineer Jobs in Boston, MA (NOW HIRING)

Semiconductor Process Engineer Location: Wilmington, MA About Us Quantum Computing Inc. (QCi) (Nasdaq: QUBT) is an innovative, integrated photonics company that provides accessible and affordable ...

Senior Legal Process Engineer

Boston, MA · On-site

$113K - $146K/yr

Senior Legal Process Engineer Cooley is seeking a Senior Legal Process Engineer to join the Practice Engineering team. Position summary : As the leading technology law firm, Cooley is determined to ...

Senior Legal Process Engineer

Boston, MA · On-site

$113K - $146K/yr

Senior Legal Process Engineer Cooley is seeking a Senior Legal Process Engineer to join the Practice Engineering team. Position summary : As the leading technology law firm, Cooley is determined to ...

Senior Process Engineer

Mansfield, MA · On-site

$110K - $142K/yr

The Senior Process Engineer is responsible to understand, optimize, and sustain manufacturing processes within a value stream leveraging lean and six sigma tools and methodologies to improve ...

Senior Process Engineer

Boston, MA · On-site

$120K - $180K/yr

Senior Process Engineer | Boston, MA | $120 - 180k We are partnered with a company that produces advanced materials with enhanced energy transfer properties using its patented Z-axis Carbon Fiber ...

ACCELERATING YOUR FUTURE The Process Engineer I/II , as a key member of the MS&T team, will develop and execute technology transfer plans for RoslinCT's partner programs, including collaborating with ...

Senior Process Engineer

Boston, MA · On-site

$120K - $180K/yr

Senior Process Engineer | Boston, MA | $120 - 180k We are partnered with a company that produces advanced materials with enhanced energy transfer properties using its patented Z-axis Carbon Fiber ...

Overview The Lead Process Engineer position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team for a client in the Greater Boston area . Outsourced ...

Lead Process Engineer

Boston, MA · On-site

$120K - $160K/yr

Overview The Lead Process Engineer position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team for a client in the Greater Boston area . Outsourced ...

Senior Process Engineer

Rockland, MA

$110K - $143K/yr

We're seeking a Senior Process Engineer who's ready to be part of a company committed to formulating everyday success for every customer through innovative, reliable products used to adhere, seal ...

Manufacturing Process Engineer

Boston, MA · On-site

$79K - $106K/yr

Process Engineering Fundamentals : Strong command of PFD (Process Flow Diagrams), time studies, line balancing, and P-FMEA. * Design for Manufacturing (DFM) : Capable of analyzing product designs and ...

Senior Process Engineer

Rockland, MA · On-site

$110K - $143K/yr

We're seeking a Senior Process Engineer who's ready to be part of a company committed to formulating everyday success for every customer through innovative, reliable products used to adhere, seal ...

This engineer will join a team in the clinical and commercial development of the processes used to manufacture sustained release hydrogel drug products. This role includes but is not limited to ...

Process Engineer II

Mansfield, MA · On-site

$71K - $97K/yr

The Process Engineer II is responsible to understand, optimize, and sustain manufacturing processes within a value stream leveraging lean and six sigma tools and methodologies to improve processing ...

Process Engineer II

Framingham, MA · On-site

$60 - $65/hr

OR a Master's degree with a minimum of 1+ years of experience in biopharmaceutical manufacturing, process engineering, or process development. * Familiarity with upstream and/or downstream bioprocess ...

Showing results 41-60

Process Engineer information

See Boston, MA salary details

$53.8K

$100K

$154.8K

How much do process engineer jobs pay per year?

As of Sep 1, 2026, the average yearly pay for process engineer in Boston, MA is $99,968.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,900.00 and $111,900.00 per year, depending on experience, location, and employer.

What is a process engineer?

Process Engineers are professionals who design, implement, and optimize industrial processes to improve efficiency, quality, and safety in manufacturing or production environments. They analyze workflows, troubleshoot process issues, and develop solutions to enhance productivity and reduce costs. Process Engineers often work in industries such as chemicals, pharmaceuticals, food and beverage, and energy, ensuring processes are compliant with environmental and safety regulations. Their work is vital for maintaining smooth operations and achieving organizational goals.

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

To thrive as a Process Engineer, you need a solid background in chemical, mechanical, or industrial engineering, often supported by a relevant bachelor's degree and understanding of process optimization principles. Familiarity with process simulation software (such as Aspen Plus or AutoCAD), Six Sigma methodologies, and quality management systems is typically required. Strong analytical thinking, problem-solving abilities, and effective communication skills set candidates apart in this role. These skills and qualifications are essential to improve efficiency, ensure safety, and drive continuous improvement in industrial and manufacturing processes.

What are some common challenges process engineers face when implementing process improvements, and how can they overcome them?

Process Engineers often encounter challenges such as resistance to change from team members, integrating new technologies with existing systems, and ensuring process changes meet regulatory standards. Overcoming these obstacles typically involves clear communication, involving stakeholders early in the process, thorough documentation, and piloting changes before full-scale implementation. Building strong cross-functional relationships and continuously gathering feedback also help ensure that improvements are effective and sustainable.

What is the difference between Process Engineer vs Manufacturing Engineer?

AspectProcess EngineerManufacturing Engineer
CredentialsBachelor's in Engineering, certifications like Six SigmaBachelor's in Engineering, certifications like Lean Manufacturing
Work EnvironmentDesigning and optimizing processes, R&D settingsOverseeing production lines, factory floors
Industry UsageManufacturing, chemical, aerospaceAutomotive, electronics, consumer goods

Process Engineers focus on designing and improving manufacturing processes, often working in R&D or engineering departments. Manufacturing Engineers concentrate on implementing and managing production on the factory floor. Both roles require similar technical skills and certifications but differ mainly in their scope and work environment.

What jobs can a process engineer do?

A process engineer designs, develops, and optimizes manufacturing processes to improve efficiency, quality, and safety. They work in industries such as chemical, pharmaceutical, food, and automotive, often using tools like process simulation software and requiring knowledge of quality standards and safety regulations.

What are the most commonly searched types of Process Engineer jobs in Boston, MA?

The most popular types of Process Engineer jobs in Boston, MA are:

What cities near Boston, MA are hiring for Process Engineer jobs?

Cities near Boston, MA with the most Process Engineer job openings:

Infographic showing various Process Engineer job openings in Boston, MA as of August 2026, with employment types broken down into 85% Full Time, and 15% Contract. Highlights an 90% In-person, 5% Hybrid, and 5% Remote job distribution, with an average salary of $99,968 per year, or $48.1 per hour.

Manufacturing Process Engineer

Piramal Pharma Limited

Lexington, MA

$82K - $110K/yr

Full-time

Re-posted 5 days ago


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.