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Internship Offshore Inspection Engineer Jobs in Boston, MA

Analog Devices

Engineer, Quality Engineering

Wilmington, MA · On-site

$78K - $101K/yr

Maintain accurate, complete, and inspection-ready training records in compliance with FDA and ISO ... Internship or co-op experience in a quality engineering role within the medical device industry ...

Analogdevices

Engineer, Quality Engineering

Wilmington, MA · On-site

$78K - $101K/yr

Maintainaccurate, complete, and inspection-ready training records in compliance with FDA and ISO ... Internship or co-op experience in a quality engineering role within the medical device industry ...

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Internship Offshore Inspection Engineer information

See Boston, MA salary details

$12

$20

$32

How much do internship offshore inspection engineer jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for internship offshore inspection engineer in Boston, MA is $20.98, according to ZipRecruiter salary data. Most workers in this role earn between $17.50 and $22.74 per hour, depending on experience, location, and employer.

What is the difference between Internship Offshore Inspection Engineer vs Offshore Inspection Engineer?

AspectInternship Offshore Inspection EngineerOffshore Inspection Engineer
QualificationsEnrolled in relevant engineering program, limited certificationsBachelor's degree in engineering, certifications like NDT or safety training
Work EnvironmentSupervised internship on offshore platforms or facilitiesFull-time role on offshore sites, independent inspections
ResponsibilitiesAssisting inspection teams, learning proceduresConducting inspections, reporting issues, ensuring safety standards

The main difference is that an Internship Offshore Inspection Engineer is a training position for students gaining practical experience, while an Offshore Inspection Engineer is a full-time professional responsible for conducting inspections independently on offshore facilities.

Internship Offshore Inspection Engineer jobs near you
Infographic showing various Internship Offshore Inspection Engineer job openings in Boston, MA as of August 2026, with employment types broken down into 90% Full Time, 5% Part Time, and 5% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $43,645 per year, or $21 per hour.

Engineer, Quality Engineering

Analog Devices

Wilmington, MA • On-site

$78K - $101K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 2 days ago

Analog Devices rating

8.5

Company rating: 8.5 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

33rd of 157 rated electronics manufacturers

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.com and 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
  • Assist in the development, implementation, and maintenance of the Medical Quality Management System (MQMS) in accordance with ISO 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.

  • Maintain accurate training records and track completion status.

  • Assist in 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.

  • Maintain accurate, complete, and inspection-ready training records in compliance with FDA and ISO requirements.

  • Identify and 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.

  • Assist in 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.

  • Help maintain history 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 or Master's degree in Biomedical Engineering, Manufacturing Engineering, Electrical Engineering, Mechanical Engineering, or a related field.

  • Understanding quality 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.

  • Proficiency in 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: Experienced
Required Travel: Yes, 10% of the time
Shift Type: 1st Shift/Days
The 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.

What Analog Devices employees say

Pay

Benefits

Hours and flexibility

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About Analog Devices

Sourced by ZipRecruiter

Analog Devices (NASDAQ: ADI) designs and manufactures semiconductor products and solutions. We enable our customers to interpret the world around us by intelligently bridging the physical and digital worlds with unmatched technologies that sense, measure and connect.

Industry

Electrical equipment, appliance, and component manufacturing

Company size

5,001 - 10,000 Employees

Headquarters location

Norwood, MA, US

Year founded

1965

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