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Biotech Engineer Jobs in Massachusetts (NOW HIRING)

Biotechnology Principal Investigator

Woburn, MA ยท On-site

$220K - $280K/yr

About the Team STR is seeking a Biotechnology Principal Investigator (PI) to develop cutting-edge ... Engineering, or related field * Experience leading technical teams on advanced R&D programs (e.g ...

Reliability Engineer

Boston, MA

$111K - $140K/yr

POSITION OVERVIEW We are seeking a Reliability Engineer to support reliability, maintenance, and asset management activities within a regulated pharmaceutical or biotechnology manufacturing ...

Showing results 41-60

Biotech Engineer information

See Massachusetts salary details

$39.9K

$117.2K

$150.2K

How much do biotech engineer jobs pay per year?

As of Sep 6, 2026, the average yearly pay for biotech engineer in Massachusetts is $117,165.00, according to ZipRecruiter salary data. Most workers in this role earn between $96,700.00 and $148,500.00 per year, depending on experience, location, and employer.

What is a biotech engineer?

Biotech Engineers are professionals who apply principles of biology, chemistry, and engineering to develop products and technologies that improve healthcare, agriculture, and the environment. They work on designing and optimizing processes for manufacturing pharmaceuticals, developing biofuels, engineering genetically modified organisms, and creating medical devices. Their work often involves research, laboratory experiments, and collaboration with other scientists and engineers to solve complex biological problems. Biotech Engineers play a key role in advancing innovations that benefit society and improve quality of life.

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

To thrive as a Biotech Engineer, you need a solid background in biology, chemistry, and engineering principles, typically supported by a degree in biotechnology, biomedical engineering, or a related field. Familiarity with laboratory instrumentation, molecular biology techniques, and data analysis software such as MATLAB or Python is essential. Strong problem-solving skills, teamwork, and effective communication set top performers apart in this interdisciplinary role. These competencies ensure successful research, product development, and innovation in the rapidly evolving biotech sector.

What are some common challenges faced by biotech engineers when working on cross-disciplinary projects?

Biotech Engineers frequently collaborate with professionals from fields like biology, chemistry, and software engineering, which can present challenges in communication and aligning project goals. Understanding the specialized terminology and priorities of each discipline is essential to ensure smooth teamwork and project success. Additionally, integrating new biotechnologies with existing systems often requires adaptability and creative problem-solving. Being open to learning from colleagues and actively seeking clarification can help overcome these challenges and lead to innovative solutions.

What is the difference between Biotech Engineer vs Biomedical Engineer?

AspectBiotech EngineerBiomedical Engineer
Required CredentialsBachelor's or Master's in Biotechnology, Bioengineering, or related fieldsBachelor's or Master's in Biomedical Engineering, Bioengineering, or related fields
Work EnvironmentBiotech companies, research labs, pharmaceutical firmsHospitals, medical device companies, research labs
Industry UsageDevelops biotech products, genetic engineering, bioprocessingDesigns medical devices, prosthetics, healthcare technology

Biotech Engineers focus on developing biotech products and processes, often working in research and manufacturing settings. Biomedical Engineers primarily design and improve medical devices and healthcare solutions. While both roles require similar educational backgrounds, their work environments and industry applications differ, catering to distinct aspects of healthcare and biotechnology.

Are biotech engineers well paid?

Biotech engineers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions often start around $60,000 to $80,000 annually, with experienced professionals earning over $100,000. Skills in laboratory techniques, data analysis, and regulatory compliance can influence earning potential.

Do biotech engineers make a lot of money?

Biotech engineers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions often start around $60,000 to $80,000 annually, with experienced professionals earning over $100,000. Skills in laboratory techniques, data analysis, and regulatory knowledge can influence earning potential.

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

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

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

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

What cities in Massachusetts are hiring for Biotech Engineer jobs?

Cities in Massachusetts with the most Biotech Engineer job openings:

Infographic showing various Biotech Engineer job openings in Massachusetts as of August 2026, with employment types broken down into 87% Full Time, 8% Part Time, and 5% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $117,165 per year, or $56.3 per hour.

PHARMACEUTICAL - MECHANICAL UTILITIES ENGINEER

MMR Consulting

Boston, MA โ€ข On-site

$120 - $180/hr

Other

Posted 25 days ago


Job description

Previous Pharmaceutical/Biotech experience is mandatory for this role.

MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical /biotechnology and highly regulated industries. Its services include Engineering, Project Management, and Validation.

MMR Consulting has offices across North America and Asia.

This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers involved in the design, commissioning & qualification, start-up and project management of various processes, systems and facilities. The work may require working out of clientโ€™s facilities, in Raleigh North Carolina.

Responsibilities
  • Provide technical guidance into the design, installation commissioning, qualification, start-up and operations of various pharmaceutical / biopharmaceutical facilities and utilities such as Purified Water (PW), Water For Injection (WFI), Clean Steam (CS), Heating, Ventilation & Air Conditioning (HVAC), Process Compressed Air (CA) & Gases
  • Lead the development of key design, technology selections, engineering and commissioning / qualification deliverables such as PFDs, P&IDs, specifications, equipment and distribution loop layouts, DQ, FAT, Commissioning Test Plans & checklists, IQ, OQ, PQ during the project lifecycle
  • Able to support detailed design development, field installation and perform field execution of commission & qualification test cases and protocols
  • Serve as technical SME on the design and operation aspects of clean utilities. Possess knowledge of regulatory requirements, mechanical specifications and industry best practices and guidelines for clean utilities.
  • Lead the design, procurement, field installation, commissioning and qualification processes throughout the project lifecycle to ensure timely completion and to ensure all quality and engineering specifications are met.
  • Support development of Project Validation Plans (PVPs) to ensure the action plan to test the system is applicable and relevant.
  • Coordinate meetings with cross-functional departments, to drive design reviews, project progress, facilitate decisions, and provide updates.
  • Travel may be occasionally required for meetings with equipment fabrication vendors or Factory Acceptance Testing (FATs).
  • Work may require occasional support over shutdowns or extended hours, specifically during installation, construction, commissioning, qualification and validation phases.
  • Visit construction and installation sites, wearing necessary safety PPE.
  • You may be involved with other aspects such as client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc.
  • Supervise contractors during critical testing of system and equipment.
  • Other duties assigned by client, and/or MMR, based on workload and project requirements.
  • As this position requires working on client sites, you will need to comply with the clientโ€™s safety rules including mandatory vaccination policies for COVID-19, where applicable
Qualifications
  • 5+ years of experience in commissioning, qualification or validation of various clean utility systems within the pharmaceutical/biotech industry.
  • Previous experience in the pharmaceutical / biotech industry, with knowledge of requirements for cGMP operations.
  • Expertise in generation, storage and distribution of pharmaceutical-grade water systems
  • Hands-on experience with industrial utilities, including:
    • Compressed air generation and distribution
    • Ammonia chillers
    • Electro boilers
    • Chilled water generation and distribution
    • Cooling water generation and distribution
    • Chilled glycol generation and distribution
    • Cooling towers
  • Hands-on experience with clean utilities, including:
    • Purified Water (PW) generation
    • Water For Injection (WFI) generation
    • Clean Steam (CS) generation
  • Hands-on experience with HVAC systems, including:
    • Air handling units (AHUs)
    • Dedicated outdoor air systems (DOAS)
    • Blower coil units
    • Air curtains
    • Computer room air conditioning (CRAC) units
    • DX cooling units
  • Experience with developing and executing validation projects to Risk-Based Commissioning & Qualification approaches, such as ASTM E-2500 or ISPE ICQ, is considered an asset.
  • Experience with commissioning and qualifications of process control systems are considered an asset.
  • Lead teams of staff, manage staff priorities, provide mentorship/oversight, help staff resolve issues. Leadership is considered an asset but not required.
  • Possess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexities.
  • Possess mentorship skills, to coach and develop junior and intermediate employees.
  • Engineering degree, preferably in Mechanical, Electrical or Chemical.
  • Travel may be required on occasion.
  • Ability to handle multiple projects and work in a fast-paced environment.
  • Strong multi-tasking skills
Equal Employment Opportunity and Reasonable Accommodations

MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.

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