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Pharma Process Engineer Jobs in Boston, MA (NOW HIRING)

PM Group

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 ... We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors.

PM Group

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 ... We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors.

Veranova

EHS-Process Safety Engineer

Harvard, MA · On-site

... for pharma and biotech customers. With deep technical expertise and impressive flexibility, we ... Partner closely with manufacturing, process engineers, engineering, maintenance and department ...

Stark Pharma Solutions Inc

Quality Engineer

Cambridge, MA · On-site

$78K - $101K/yr

You can also follow Stark Pharma Solutions on LinkedIn for the latest job updates: Job Title ... in process validation, equipment qualification, and product quality improvement initiatives.

AT Process Technologies

Process Chemist

Waltham, MA · On-site

$130K - $200K/yr

S., or PhD in Chemistry, Organic Chemistry, Chemical Engineering, or a related discipline * 5+ ... pharma, fine/specialty chemicals, or CDMO process development. * Practical mechanical and ...

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

Pharma Process Engineer information

See Boston, MA salary details

$53.8K

$100K

$154.8K

How much do pharma process engineer jobs pay per year?

As of Sep 13, 2026, the average yearly pay for pharma 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 does a Pharma Process Engineer do?

A Pharma Process Engineer designs, develops, and optimizes manufacturing processes for pharmaceutical products. They ensure that production processes are efficient, safe, and compliant with regulatory standards like Good Manufacturing Practice (GMP). Their work often involves troubleshooting equipment, scaling up production from laboratory to industrial scale, and implementing process improvements to increase yield and product quality. They also collaborate closely with quality assurance and research teams to ensure that all products meet strict safety and efficacy standards.

What are the key skills and qualifications needed to thrive as a Pharma Process Engineer?

To thrive as a Pharma Process Engineer, you need a strong background in chemical engineering or pharmaceutical sciences, often supported by a relevant degree and industry experience. Familiarity with process simulation software (such as Aspen Plus), GMP regulations, and validation protocols is typically required. Strong analytical thinking, problem-solving abilities, and effective communication skills set standout professionals apart in this field. These skills and qualities are important because they ensure safe, efficient, and compliant pharmaceutical manufacturing processes.

What are some common challenges faced by Pharma Process Engineers when optimizing manufacturing processes?

Pharma Process Engineers often encounter challenges such as maintaining strict regulatory compliance while implementing process improvements and ensuring product quality. Balancing efficiency with adherence to Good Manufacturing Practices (GMP) can be complex, especially during scale-up or technology transfer projects. Additionally, collaborating across multidisciplinary teams—including quality assurance, production, and R&D—requires strong communication skills to align objectives and resolve issues quickly. These challenges make adaptability and attention to detail crucial traits for success in the role.

What is the difference between Pharma Process Engineer vs Chemical Process Engineer?

AspectPharma Process EngineerChemical Process Engineer
Required CredentialsBachelor's in Chemical, Pharmaceutical, or related field; GMP certification often preferredBachelor's in Chemical Engineering or related field; Professional Engineer (PE) license optional
Work EnvironmentPharmaceutical manufacturing facilities, labs, cleanroomsChemical plants, refineries, manufacturing sites
Industry UsagePharmaceutical, biotech, healthcareChemical, petrochemical, manufacturing
Common Search/ComparisonYesYes

Both Pharma Process Engineers and Chemical Process Engineers work in manufacturing environments requiring chemical engineering knowledge. Pharma Process Engineers focus on pharmaceutical production, adhering to strict GMP standards, while Chemical Process Engineers work across various chemical industries. Their roles overlap in process design and optimization, but Pharma Process Engineers specialize in drug manufacturing processes.

What are popular job titles related to Pharma Process Engineer jobs in Boston, MA?

For Pharma Process Engineer jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Pharma Process Engineer jobs in Boston, MA look for?

The top searched job categories for Pharma Process Engineer jobs in Boston, MA are:

Pharma Process Engineer jobs near you
Infographic showing various Pharma Process Engineer job openings in Boston, MA as of September 2026, with employment types broken down into 63% Full Time, 5% Part Time, and 32% Contract. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $99,968 per year, or $48.1 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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