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Microfluidic Engineer Jobs in Boston, MA (NOW HIRING)

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Microfluidic Engineer information

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$49.4K

$111.8K

$180.9K

How much do microfluidic engineer jobs pay per year?

As of Aug 7, 2026, the average yearly pay for microfluidic engineer in Boston, MA is $111,767.00, according to ZipRecruiter salary data. Most workers in this role earn between $88,500.00 and $137,400.00 per year, depending on experience, location, and employer.

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

To thrive as a Microfluidic Engineer, you need a solid background in engineering, physics, or biomedical sciences, with expertise in fluid dynamics, microfabrication, and device prototyping. Familiarity with CAD software, cleanroom processes, simulation tools like COMSOL Multiphysics, and often a relevant certification or advanced degree are commonly valued. Strong analytical thinking, problem-solving, and collaboration skills are crucial, as projects frequently involve interdisciplinary teams. These competencies are important for successfully designing, developing, and troubleshooting innovative microfluidic devices used in fields like life sciences, diagnostics, and research.

What are typical daily responsibilities for a microfluidic engineer?

A Microfluidic Engineer's daily responsibilities often include designing and simulating microfluidic systems, conducting laboratory experiments, analyzing prototype performance, and working closely with biologists, chemists, and other engineers to refine project requirements. They may also spend time fabricating devices in cleanroom environments, documenting results, and troubleshooting technical challenges that arise during development. Collaboration with team members and stakeholders is common, as is the need to stay up-to-date on advancements in fabrication techniques and materials. These activities ensure that innovative and reliable microfluidic solutions are created for applications ranging from medical diagnostics to drug development.

What is a microfluidic engineer?

A Microfluidic Engineer designs, develops, and optimizes microfluidic systems for applications in biotechnology, healthcare, diagnostics, and research. They work with small-scale fluid dynamics, creating devices that manipulate tiny volumes of liquids for tasks like lab-on-a-chip technology, drug delivery, and chemical analysis. Their role involves material selection, prototyping, testing, and integrating microfluidic systems with sensors and electronics. They often collaborate with biologists, chemists, and engineers to develop innovative solutions for scientific and industrial challenges.

What job categories do people searching Microfluidic Engineer jobs in Boston, MA look for? The top searched job categories for Microfluidic Engineer jobs in Boston, MA are:
What cities near Boston, MA are hiring for Microfluidic Engineer jobs? Cities near Boston, MA with the most Microfluidic Engineer job openings:
Infographic showing various Microfluidic Engineer job openings in Boston, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 93% In-person, and 7% Hybrid job distribution, with an average salary of $111,767 per year, or $53.7 per hour.

Senior Product Development Engineer -Mechanical Engineering (Hybrid Boston)

Haemonetics Corporation

Boston, MA • On-site

$78K - $133K/yr

Full-time

Medical, Retirement, PTO

Re-posted 16 days ago


Haemonetics rating

8.0

Company rating: 8.0 out of 10

Based on 10 frontline employees who took The Breakroom Quiz


Job description

Pay Transparency:
The pay range for this role is:
$78,400.00-$133,400.00/Annual
The base pay actually offered to the successful candidate will take into account, without limitation, the candidate's location, education, job-knowledge, skills, and experience in prior relevant roles.
Incentives may also be provided as part of Haemonetics' employee compensation. For sales roles, employees will be eligible for sales incentive (i.e., commission) under the applicable plan terms. For non-sales roles, employees will be eligible for a discretionary annual bonus, the target amount of which varies based on the applicable role, to be governed by the applicable plan terms. Employees may also be eligible to participate in the Company's long-term incentive plan, with eligibility and target amount dependent on the role.
In addition to compensation, the Company offers a competitive suite of benefits to its employees, including without limitation, a 401(k) with up to a 6% employer match and no vesting period, an employee stock purchase plan, "flexible time off" for salaried employees and, for hourly employees, accrual of three to five weeks' vacation annually (based on tenure), accrual of up to 64 hours (annually) of paid sick time, paid and/or floating holidays, parental leave, short- and long-term disability insurance, tuition reimbursement, and/or health and welfare benefits.
Depending on your location, you may be eligible for more detailed information related to the compensation and benefits related to this job posting. If you believe you may be entitled to such information by law, you may contact 1-781-348-7777, Monday through Friday, 7:30 a.m. - 5 p.m. ET or email AskHR@Haemonetics.com.
We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further - Haemonetics is your employer of choice.
Job Details
Job Summary: We are seeking a Senior Product Development Engineer with strong mechanical design experience to lead the design and development of disposable device components for an in-vitro diagnostic platform. This role requires hands-on ownership of plastic part design, injection molded components, design specifications, drawings, tolerance analysis, verification planning, and design transfer for high-volume disposable manufacturing. The ideal candidate will combine strong mechanical design fundamentals with experience working directly with suppliers, tooling vendors, and contract manufacturers in a regulated medical device environment.
Key Responsibilities:
• Lead mechanical design of disposable device components from concept through production, including CAD modeling, design specifications, drawings, tolerance analysis, GD&T, and verification planning.
• Design plastic components for high-volume manufacturing, with emphasis on injection molding, manufacturability, dimensional control, component robustness, cost, and scalability.
• Partner with suppliers, tooling vendors, and contract manufacturers to evaluate design tradeoffs, resolve manufacturability issues, support process validation, and transition designs into production.
• Own sustaining activities for disposable components and serve as the technical lead for manufacturing and supplier component performance issues, including design change requests.
• Develop and execute verification strategies, test protocols, engineering studies, and reports to demonstrate performance against design requirements.
• Create and maintain design control documentation, including requirements, specifications, drawings, risk documentation, design reviews, investigations, and regulatory inputs.
• Collaborate across engineering, manufacturing, quality, regulatory, procurement, and commercial teams while providing technical guidance to junior engineers and cross-functional partners.
Primary Qualifications:
• Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related technical discipline.
• 5+ years of product development experience in medical device, IVD, life sciences, diagnostics, or another regulated product development environment.
• Demonstrated experience with mechanical component design, plastic part design, injection molded components, high-volume disposable manufacturing, CAD, engineering drawings, verification testing, and design transfer; Proficiency with 3D CAD tools such as SolidWorks and experience with engineering drawings, BOMs, ECOs, and PLM or document control systems.
• Experience working with suppliers, tooling vendors, and contract manufacturers to support part qualification, manufacturing transfer, and production issue resolution.
Preferred Qualifications:
• Experience with microfluidic, cartridge-based, fluidic, electromechanical, or disposable diagnostic systems.
• Familiarity with design controls, risk management, verification and validation, process validation, and regulated medical device documentation.
Skills & Competencies: Strong mechanical design judgment, clear cross-functional communication, supplier collaboration, technical problem solving, data-driven decision-making, and the ability to lead ambiguous design and manufacturing challenges.
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