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Climate Engineering Jobs in Boston, MA (NOW HIRING)

Analogdevices

Engineer, Quality Engineering

Wilmington, MA · On-site

$78K - $101K/yr

ADI combines analog, digital, AI, and software technologies into solutions that combat climate ... The position also includes responsibilities as a Training Coordinator for the Quality Engineering ...

CDM Smith

Water Resources Engineer 6

Boston, MA

$85K - $117K/yr

... climate resilience, watershed planning, dams, coastal systems, ecosystem restoration, water supply, and related infrastructure. * Apply your technical expertise and engineering judgment to develop ...

CDM Smith

Water Resources Engineer 6

Boston, MA · On-site

$85K - $117K/yr

... climate resilience, watershed planning, dams, coastal systems, ecosystem restoration, water supply, and related infrastructure. * Apply your technical expertise and engineering judgment to develop ...

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Climate Engineering information

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$34

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How much do climate engineering jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for climate engineering in Boston, MA is $34.28, according to ZipRecruiter salary data. Most workers in this role earn between $21.92 and $41.25 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of a climate engineering professional?

Climate Engineering professionals typically analyze environmental data, develop and model climate intervention strategies, and oversee project implementation to mitigate or adapt to climate change effects. They often collaborate with scientists, policymakers, and engineers from related fields to ensure project success and regulatory compliance. Daily tasks may include running simulations, preparing technical reports, conducting field studies, and presenting findings to stakeholders. This role frequently involves both office-based analytical work and occasional site visits, offering a dynamic and impactful work environment for those passionate about environmental solutions.

What is climate engineering?

A Climate Engineering job involves developing and implementing technologies to mitigate or reverse climate change. Professionals in this field work on solutions like carbon capture, solar geoengineering, and sustainable infrastructure. They often have backgrounds in environmental science, engineering, or atmospheric studies. The goal is to reduce greenhouse gas emissions and manage climate risks while balancing ecological and societal impacts.

What are the key skills and qualifications needed to thrive in climate engineering, and why are they important?

To thrive in Climate Engineering, a solid background in environmental science, engineering principles, and sustainability—often supported by an advanced degree in a relevant field—is essential. Familiarity with climate modeling software, Geographic Information Systems (GIS), and certifications in environmental or engineering disciplines are commonly required. Strong analytical thinking, problem-solving, and effective communication skills help individuals collaborate and convey complex concepts to diverse stakeholders. These capabilities ensure that climate engineers can design, implement, and oversee impactful projects that address complex environmental challenges.

What are popular job titles related to Climate Engineering jobs in Boston, MA?

For Climate Engineering jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Climate Engineering jobs in Boston, MA look for?

The top searched job categories for Climate Engineering jobs in Boston, MA are:

Climate Engineering jobs near you
Infographic showing various Climate Engineering job openings in Boston, MA as of August 2026, with employment types broken down into 88% Full Time, 6% Part Time, 5% Contract, and 1% Nights. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $71,294 per year, or $34.3 per hour.

Engineer, Quality Engineering

Analogdevices

Wilmington, MA • On-site

$78K - $101K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 28 days ago

Job description

About Analog Devices

Analog Devices, Inc. (NASDAQ: ADI) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, AI, and software technologies into solutions that combat climate change, reliably connect humans and the world, and help drive advancements in automation and robotics, mobility, healthcare, energy and data centers. With revenue of more than $11 billion in FY25, ADI ensures today's innovators stay Ahead of What's Possible. Learn more at www.analog.comand on LinkedIn and X.

We are seeking a motivated Quality Systems Engineer to join our team. This role supports the development, implementation, and maintenance of quality management systems for medical devices, ensuring compliance with ISO 13485, FDA regulations, and EU MDR. The position also includes responsibilities as a Training Coordinator for the Quality Engineering group.

Key Responsibilities

  • Assistin the development, implementation, and maintenance of the Medical Quality Management System (MQMS)in accordance withISO 13485, 21 CFR 820, EU MDR, and other applicable standards.
  • Support quality system processes including CAPA, Internal Audits, Document Control, Change Management, Training, and Management Review.
  • Support the coordination and administration of training activities:
  • Organize and schedule training sessions for team members or stakeholders.
  • Maintainaccuratetraining records and track completion status.
  • Assistin the development of training materials and in evaluating the effectiveness of training programs.
  • Coordinate and administer initial, ongoing, and re-training activities for employees, contractors, and temporary personnel.
  • Assign and track mandatory quality, regulatory, and job-specific training per approved procedures and curricula.
  • Maintainaccurate, complete, and inspection-ready training records in compliance with FDA and ISO requirements.
  • Identifyand coordinate retraining needs resulting from SOP, process, product, or regulatory changes
  • Participate in internal and external audits, ensuring compliance with regulatory standards.
  • Conduct root cause analysis and implement corrective and preventive actions (CAPA) to address quality issues.
  • Collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to ensure product quality and safety.
  • Perform risk assessments and support the development of risk management plans.
  • Review and approve quality documentation, including SOPs, work instructions, and validation protocols.
  • Support the investigation and resolution of customer complaints and non-conformances.
  • Assistin the preparation of quality reports and metrics for management review.
  • Support compliance with 21 CFR Part 11 for electronic records and signatures,including validation and oversight of quality system software tools.
  • Helpmaintainhistory files, risk management documentation, and post-market surveillance processes.
  • Participate in root cause investigations and failure analysis efforts using quality tools and methodologies.
  • Support validation planning and execution for new product designs and manufacturing processes.

Qualifications

  • Bachelor's orMaster's degree in Biomedical Engineering, Manufacturing Engineering, Electrical Engineering, Mechanical Engineering, ora relatedfield.
  • Understandingquality management principles and regulatory requirements in the medical device industry.
  • Excellent analytical and problem-solving skills.
  • Effective communication and interpersonal skills.
  • Ability to work independently and as part of a team.
  • Proficiencyin Microsoft Office Suite and quality management software.
  • Familiarity with regulatory requirements including US CFR (Code of Federal Regulation), ISO (International Organization for Standardization), GMP (Good Manufacturing Practice), and EU MDR (Medical Device Regulation).
  • Knowledge of FDA 510(k) clearance, FDA Premarket Approval (PMA), and ongoing submission maintenance requirements.
  • Internship or co-op experience in a quality engineering role within the medical device industry (preferred).
  • Knowledge of statistical analysis and quality improvement tools (e.g., Six Sigma, Lean) (preferred).

For positions requiring access to technical data, Analog Devices, Inc. may have to obtain export licensing approval from the U.S. Department of Commerce - Bureau of Industry and Security and/or the U.S. Department of State - Directorate of Defense Trade Controls. As such, applicants for this position - except US Citizens, US Permanent Residents, and protected individuals as defined by 8 U.S.C. 1324b(a)(3) - may have to go through an export licensing review process.

Analog Devices is an equal opportunity employer. We foster a culture where everyone has an opportunity to succeed regardless of their race, color, religion, age, ancestry, national origin, social or ethnic origin, sex, sexual orientation, gender, gender identity, gender expression, marital status, pregnancy, parental status, disability, medical condition, genetic information, military or veteran status, union membership, and political affiliation, or any other legally protected group.

EEO is the Law: Notice of Applicant Rights Under the Law.

Job Req Type: ExperiencedRequired Travel: Yes, 10% of the timeShift Type: 1st Shift/DaysThe expected wage range for a new hire into this position is $75,200 to $103,400.

  • Actual wage offered may vary depending on work location, experience, education, training, external market data, internal pay equity, or other bona fide factors.

  • This position qualifies for a discretionary performance-based bonus which is based on personal and company factors.

  • This position includes medical, vision and dental coverage, 401k, paid vacation, holidays, and sick time, and other benefits.

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