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Pharmaceutical Project Engineer Jobs in Massachusetts

Experience in the pharmaceutical industry is highly preferred. * Ability to review and approve project documents related to mechanical engineering deliverables. * Knowledge of FDA, GMP, ASME, BPE ...

Arcadis is seeking a Project Engineer to work with a pharmaceutical client in the Boston, MA area. The ideal candidate has engineering experience in a GMP environment and will provide day-to-day ...

... Project Engineer is responsible for delivering practical engineering support during the design ... pharmaceutical manufacturing facility. 3 years' experience in an aseptic and/or powder ...

Project Engineer

Ayer, MA · On-site

$86K - $106K/yr

... pharmaceutical manufacturing facility. • 3 years' experience in an aseptic and/or powder ... project engineer should have the ability to proactively troubleshoot and possess the desire to ...

... pharmaceutical manufacturing facility. • 3 years' experience in an aseptic and/or powder ... project engineer should have the ability to proactively troubleshoot and possess the desire to ...

Overview The Project Engineer - Capital Projects position is an exciting opportunity to join PM ... Experience in pharmaceutical, biotech, or life sciences environments strongly preferred

Packaging Project Engineer

Tewksbury, MA · On-site

$84K - $116K/yr

Projects include new packaging design, material conversions/down gauging, quality improvements, and ... packaging engineer in the medical device, pharmaceutical, or life sciences industry.

Mechanical Engineer / Project Engineer (Mid Level) Do you have an innate curiosity when it comes to ... Ranked #5 in Pharmaceutical Design by ENR magazine, we're designing and constructing facilities ...

Mechanical Engineer / Project Engineer (Mid Level) Do you have an innate curiosity when it comes to ... Ranked #5 in Pharmaceutical Design by ENR magazine, we're designing and constructing facilities ...

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Pharmaceutical Project Engineer information

What does a pharmaceutical project engineer do?

A Pharmaceutical Project Engineer is responsible for planning, coordinating, and overseeing engineering projects within pharmaceutical manufacturing or research facilities. Their work includes designing and implementing new production processes, managing equipment installations, ensuring compliance with industry regulations, and optimizing operations for efficiency and safety. They often collaborate with cross-functional teams such as quality assurance, validation, and production to make sure projects are completed on time and within budget.

How does a pharmaceutical project engineer typically collaborate with cross-functional teams during a project lifecycle?

Pharmaceutical Project Engineers work closely with cross-functional teams, including quality assurance, regulatory affairs, production, and R&D, to ensure that projects meet industry standards and compliance requirements. They often facilitate communication between departments, manage timelines, and coordinate technical solutions to address challenges that arise. This collaborative approach is key to delivering projects on time while adhering to strict safety and regulatory guidelines. Effective teamwork and communication skills are essential, as engineers must align diverse stakeholders and maintain project momentum.

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

To thrive as a Pharmaceutical Project Engineer, you need a solid background in engineering (usually a degree in chemical, mechanical, or process engineering), combined with knowledge of pharmaceutical manufacturing processes and regulatory standards. Familiarity with project management software, CAD tools, and validation protocols, along with certifications like PMP or Six Sigma, is often required. Excellent problem-solving, communication, and teamwork skills help manage cross-functional teams and address complex project challenges. These skills and qualifications are crucial to ensure projects are delivered efficiently, safely, and in compliance with industry regulations.

What is the difference between Pharmaceutical Project Engineer vs Pharmaceutical Manufacturing Specialist?

AspectPharmaceutical Project EngineerPharmaceutical Manufacturing Specialist
CredentialsBachelor's in Engineering, Project Management certificationsTechnical degree, GMP training, certifications in manufacturing processes
Work EnvironmentEngineering offices, labs, manufacturing plantsManufacturing floors, quality control labs
Employer & Industry UsagePharmaceutical companies, biotech firmsPharmaceutical manufacturing facilities, contract manufacturers
Primary FocusPlanning, executing, and managing engineering projectsEnsuring manufacturing processes meet quality and compliance standards

The Pharmaceutical Project Engineer focuses on managing engineering projects within pharmaceutical companies, overseeing design, installation, and process improvements. In contrast, the Pharmaceutical Manufacturing Specialist concentrates on the day-to-day operations of manufacturing processes, ensuring quality and compliance. Both roles are essential in pharmaceutical production but differ in scope and responsibilities.

What are popular job titles related to Pharmaceutical Project Engineer jobs in Massachusetts?

For Pharmaceutical Project Engineer jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Project Engineer jobs in Massachusetts look for?

The top searched job categories for Pharmaceutical Project Engineer jobs in Massachusetts are:

Infographic showing various Pharmaceutical Project Engineer job openings in Massachusetts as of August 2026, with employment types broken down into 69% Full Time, 5% Temporary, and 26% Contract. Highlights an 100% In-person job distribution.

Full-time

Re-posted 6 days ago


Job description

Discover your exciting role

Exentec BioPharma Solutions is seeking an experienced Manufacturing Project Engineer in Lawrence, MA, to work closely with the operations teams on custom TFF, chromatography, and related hardware systems. This role serves as a key technical resource, evaluating customer specifications and translating them into mechanical designs that comply with ASME, BPE, FDA, and other applicable standards.

Explore your tasks and responsibilities
  • Define, engineer, specify, plan, and manage all mechanical activities related to assigned projects.
  • Support manufacturing and qualification activities to ensure mechanical requirements are met.
  • Perform mechanical analyses of filtration and chromatography systems.
  • Specify components based on customer requirements while maintaining cost and schedule controls within project scope.
  • Plan, organize, and execute system powerup activities in coordination with staff electricians.
  • Interface effectively with customers and internal project teams to communicate needs, expectations, and capabilities.
  • Support sales efforts, including customer visits, to help define specifications and project scope.
  • Evaluate quote requests, assess feasibility, and prepare quotations according to established procedures.
  • Identify required tools and resources to support quotation and project activities.
  • Maintain familiarity with European and U.S. codes and standards (ASME, BPE, XP, ATEX, CE, etc.).
  • Seek and evaluate new tools, components, or technologies that improve design efficiency.
  • Provide consistent communication and feedback to project teams, manufacturing, and customers.
  • Other duties as assigned.
Show your expertise
  • A bachelor's degree in Mechanical Engineering is required.
  • 1-2 years of engineering experience, ideally involving capital equipment.
  • Experience in the pharmaceutical industry is highly preferred.
  • Ability to review and approve project documents related to mechanical engineering deliverables.
  • Knowledge of FDA, GMP, ASME, BPE, and CE regulations and guidelines, with the ability to apply them appropriately.
  • Proficiency in AutoCAD for drafting parts and creating P&IDs.
  • Ability to stay current with internal and external technologies relevant to Exentec's systems.
  • Experience in a manufacturing environment, preferably within the biotechnology or pharmaceutical industry.
  • Strong computer skills, including MS Office 365, Project, SharePoint, and AutoCAD.

About Exentec BioPharma Solutions
Exentec BioPharma Solutions specializes in customengineered process separation and fluidhandling equipment for the biopharmaceutical industry. Our design, engineering, and project management teams focus on delivering tailored solutions that meet stringent industry and client requirements.

Non-Solicitation
We are not currently accepting third-party agency candidates for this position. Any agency candidate submitted to any employee of Exyte, or its subsidiaries, may be contacted by Exyte, or its subsidiaries, without obligation to the third-party agency.


Employment Sponsorship
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor employment visas at this time.


EEO Statement
Exyte US, Inc. and its subsidiaries are proud to be an Equal Employment Opportunity employer that is committed to supporting an inclusive workplace where associates excel based on personal merit, qualifications, experience, ability, and job performance. We prohibit discrimination and harassment of any kind based on race, color, religion, age, sex (e.g., pregnancy, childbirth and related medical conditions, sexual orientation, gender identity), national origin, disability, genetic information, protected veteran status, or any other protected characteristic as outlined by applicable federal, state, or local laws.

Contact:

You want to be part of the Exyte team? We look forward to receiving your application!

Please note that we only consider applications submitted through our application portal. Applications sent via email will not be considered due to data protection regulations.

Employment Type: FULL_TIME