Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Quality Engineer - FDA Regulated, Up to $120K (01754)

$120k

Adecco Staffing

Senior Quality Engineer

Location: Devens, MA
Job Type: Direct Hire / Full-Time
Salary: $100,000, annually
Industry: Medical Device / Regulated Manufacturing

Lead Quality. Drive Compliance. Make an Impact.

Adecco is hiring a Senior Quality Engineer for a leading manufacturer in Devens, MA!

This is an exciting opportunity for an experienced Quality Engineer to take on a key role within a regulated manufacturing environment. You'll work across Quality, Engineering, R&D, Manufacturing, and Regulatory teams to ensure products and processes meet the highest standards for quality, safety, and compliance.

If you have strong experience in medical devices, FDA regulations, ISO standards, process validation, CAPA, and risk management , this could be an excellent opportunity to take the next step in your career.

What You'll Do

  • Oversee Design History Files (DHF) , design verification activities, and risk management documentation in accordance with ISO 14971

  • Lead and approve IQ/OQ/PQ process validations , manufacturing validations, and test method validations.

  • Apply statistical tools including SPC and DOE to evaluate and improve manufacturing processes.

  • Manage Non-Conformances (NCRs), CAPAs, and failure investigations from identification through resolution.

  • Partner with R&D, Manufacturing, Quality, and Regulatory teams during New Product Introduction (NPI), product development, and product changes.

  • Support and participate in internal and external audits

  • Help ensure compliance with FDA 21 CFR Part 820 and applicable quality system requirements.

  • Identify opportunities for continuous improvement and help strengthen quality processes across the organization.

  • Provide technical quality support and guidance to cross-functional teams throughout the product lifecycle.

What You'll Bring

  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, or a related technical field.

  • Master's degree preferred.

  • 5–8+ years of experience in medical device manufacturing or another highly regulated industry.

  • Strong knowledge of FDA Quality System Regulations (QSR)

  • Strong understanding of ISO 13485 and ISO 14971

  • Hands-on experience with process validation, risk management, CAPA, NCRs, and failure investigations

  • Experience with statistical analysis and quality tools such as SPC and DOE

  • Strong communication and cross-functional collaboration skills.

  • Ability to effectively manage multiple projects and priorities in a regulated manufacturing environment.

Why Consider This Opportunity?

This is more than a traditional Quality Engineering role. As a Senior Quality Engineer , you'll have the opportunity to influence product quality, manufacturing processes, compliance, and continuous improvement while working alongside experienced Engineering, R&D, Manufacturing, and Regulatory professionals.

If you're ready to bring your quality expertise to a role where your work directly supports product reliability, regulatory compliance, and manufacturing excellence , apply today!

Pay Details: $100,000.00 per year

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal Opportunity Employer/Veterans/Disabled

Military connected talent encouraged to apply

To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to

The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:

  • The California Fair Chance Act
  • Los Angeles City Fair Chance Ordinance
  • Los Angeles County Fair Chance Ordinance for Employers
  • San Francisco Fair Chance Ordinance

Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Vacancy posted 16 days ago
Similar jobs that could be interesting for youBased on the Quality Engineer - FDA Regulated, Up to $120K (01754) in Maynard, MA vacancy
  • $25 - $34 per hour

    Job SummaryCo-op, Quality Engineering: January-June (Onsite) Position Overview: Position Dates: January 11, 2027 - June 30, 2027 The Quality...  ...tools, and cross-functional collaboration within a regulated environment.Responsibilities: Analyze quality and operational... 
    Suggested
    Full time
    Internship

    Insulet Corporation

    Acton, MA
    2 days ago
  • $87.3k - $130.95k

    Job SummaryThe Senior Quality Assurance Engineer is responsible for ensuring quality, compliance, and continuous improvement within the manufacturing...  ...improvement initiatives while ensuring compliance with FDA regulations, ISO 13485, and Insulet’s Quality System. Working... 
    Suggested
    Full time
    Contract work
    Work at office
    Worldwide

    Insulet Corporation

    Acton, MA
    5 days ago
  •  ...customers worldwide. We have an exciting opportunity for a Quality Engineer to join our team in Acton, MA! The Quality Engineer...  ...interpreting and adapting quality standards and government regulations. Collaborates with engineering and manufacturing to ensure quality... 
    Suggested
    Full time
    Contract work
    Part time
    Local area
    Worldwide
    Relocation package

    General Atomics

    Acton, MA
    1 day ago
  •  ...Quality Engineer General Atomics Electromagnetic Systems (GA-EMS) designs and manufactures first-of-a-kind electromagnetic and electric...  ...interpreting and adapting quality standards and government regulations. Collaborates with engineering and manufacturing to ensure quality... 
    Suggested
    Worldwide

    General Atomics Integrated Intelligence

    Acton, MA
    4 days ago
  • Job Summary The Quality Engineer, NGP Programs is responsible for supporting quality engineering activities to facilitate early...  ...controls and readiness assessments. Ensure compliance with FDA Quality System Regulations, ISO 13485, GMP requirements, and applicable regulatory... 
    Suggested

    Insulet Corporation

    Acton, MA
    2 days ago
  • $25 - $34 per hour

    Job SummaryCo-op, Embedded Software Test Engineering - Embedded Software (Manual & Automation...  ...for embedded software systems in regulated medical devices. This role involves designing...  ...collaborate and participate in test execution and quality alignment.This position assists in the... 
    Full time
    Flexible hours

    Insulet Corporation

    Acton, MA
    1 day ago
  • Recruiter: Spencer Gregory HaleSupplier Quality Engineer II - Endoscopy SFMD About the role: The Sourced Finished Medical Device (SFMD) Supplier...  ...years of quality engineering experience within a different regulated industry). Experience in medical device, automotive,... 
    Hourly pay
    Shift work

    Boston Scientific Corporation

    Marlborough, MA
    3 days ago
  • What You’ll DoThe Senior Quality Engineer is responsible for supporting the effective establishment...  ....Conduct gap analyses for new/updated regulations and standards; develop plans and...  ...It TakesRequires thorough knowledge of FDA, ISO, and other regulatory guidelines related... 
    Full time
    Work at office
    Immediate start

    Anika

    Bedford, MA
    5 days ago
  • $95.5k - $181.7k

     ...the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today’s mission and stay ahead...  ...of aerospace and defense.Join our team as a Program Supplier Quality Engineer (PSQE) supporting the Advanced Technology (AT) Strategic... 
    Temporary work
    Work experience placement
    Work at office
    Remote work
    Flexible hours

    Raytheon

    Sudbury, MA
    2 days ago
  • $107.5k - $204.5k

     ...the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today’s mission and stay ahead...  ...a safer, more secure world.Join our team as a Senior Program Quality Engineer (PQE) supporting the Advanced Technology (AT) Strategic... 
    Temporary work
    Work experience placement
    For subcontractor
    Work at office
    Remote work
    Relocation package
    Flexible hours

    Raytheon

    Sudbury, MA
    3 days ago
  • Recruiter: Spencer Gregory HaleQuality Systems Engineer IIIAbout the role:The Quality Systems Engineer III supports the Global Quality Systems and...  ...maintain audit readiness in accordance with applicable regulations and standards, including ISO 13485, 21 CFR Part 820 and... 
    Hourly pay
    Permanent employment
    Work at office
    Local area
    Relocation
    Relocation package
    Shift work
    3 days per week

    Boston Scientific Corporation

    Marlborough, MA
    5 days ago
  •  ...Senior Quality Systems Engineer Of Material Controls At Boston Scientific, we'll give you the opportunity...  ...ensuring compliance to Medical Device regulations and BSC Quality System requirements....  ...System Requirements (ISO 13485) and FDA Quality System Regulation (21 CFR Part... 
    Work at office
    Local area
    Relocation package
    3 days per week

    Intracept by Boston Scientific

    Marlborough, MA
    2 days ago
  • $102.48k - $163.97k

     ...The Senior Quality Systems Engineer is responsible for ensuring an efficient/compliant Quality Management...  ...to enhance understanding of industry regulations and best practices. Cultivates...  ...a minimum of 5+ years’ experience in FDA/ISO 13485 medical device quality operations... 
    Full time
    Work at office
    Local area
    Work visa
    Relocation package
    3 days per week

    Philips

    Bedford, MA
    3 days ago
  •  ...Senior Quality Systems Engineer Work mode: Hybrid Onsite Location(s): Arden Hills, MN, US, 55112...  ...ensuring compliance to Medical Device regulations and BSC Quality System requirements....  ...compliance with global BSC processes, FDA regulations, ISO 13485, and Medical Device... 
    Work at office
    Local area
    Relocation package
    3 days per week

    Boston Scientific

    Marlborough, MA
    4 days ago
  • $150k - $170k

     ...Job Summary: The Sr. Quality Control Manager is responsible...  ...control strategies that support FDA medical device requirements,...  ...Manufacturing, Manufacturing Engineering, Finished Goods, and Distribution...  ...experience within an FDA-regulated medical device, IVD, or reagent... 
    Hourly pay
    Work at office
    Flexible hours
    Shift work

    Nova Biomedical

    Waltham, MA
    2 days ago
  •  ...On-Site We have an exceptional opportunity for a Quality Engineer to join our team in the Boxborough, MA facility. This individual would...  ...to read and interpret documents such as blue prints, regulations, and quality system related procedure manuals and standards.... 
    Internship
    Local area

    Ralliant

    Boxborough, MA
    4 days ago
  • $80k - $85k

     ...JOB SUMMARY TekniPlex is hiring a Quality Engineer for our Ashland, MA facility. This role...  ...ISO 13485, ISO 9001, GMP, and applicable FDA/21 CFR requirements. Plan, host, and...  ...Supervisory or leadership experience in a regulated manufacturing environment is preferred.... 
    Daily paid
    Temporary work
    For contractors
    Local area
    Immediate start
    Flexible hours
    Shift work

    Tekni-Plex

    Ashland, MA
    4 days ago
  • $150k - $180k

     ...compliance with procedures, standards and regulations applicable to our products. Job...  ...tools and practices to achieve product quality goals and requirements in the areas of...  ...Education: Bachelor's degree or equivalent in engineering or science Experience: A minimum of... 

    Werfen

    Bedford, MA
    2 days ago
  • $86.8k - $165.2k

     ...Systems (ATS) organization has an immediate need for a Senior Quality Engineer within our ATS team. As a Senior Quality Engineer, you will...  ...concepts and general understanding of aerospace/defense regulations and standards. Critical-thinking skills and the ability to... 
    Contract work
    Temporary work
    Work experience placement
    Work at office
    Immediate start
    Remote work
    Relocation package
    Flexible hours

    Raytheon Technologies

    Marlborough, MA
    3 days ago
  •  ...contains Catheter and Console (System) products. Manufacture engineering, Product Quality, and/or SQE with this hands-on experience in Process...  ..., customer complaints, industry standards and government regulations. You're the right fit if: • Bachelor Degree engineering... 
    Local area

    Info Way Solutions

    Bedford, MA
    4 days ago
  • $103k - $163k

     ...The Supplier Quality Engineer is a key member of Philips’ Image Guided Therapy Devices (IGTD)...  ...complaints, industry standards and government regulations. Provide Quality oversight of...  ...in Supplier Quality Engineering within FDA regulated medical device environments,... 
    Full time
    Work at office
    Local area
    Work visa
    Relocation package
    3 days per week

    Philips

    Bedford, MA
    3 days ago
  •  ...Supplier Quality Engineer Web Industries, a 100% employee-owned company (ESOP), brings a lot of advantages to the people who work here...  ...automotive, aerospace, defense, medical device, or another highly regulated manufacturing environment, including familiarity with... 
    Permanent employment
    Work at office

    Web Industries

    Marlborough, MA
    5 days ago
  • $75.41k - $103.69k

     ...Job Purpose As a Quality Systems Engineer, you will be responsible for helping to ensure the QMS is...  ...prescribed procedures, policies, and regulations. Key Responsibilities Ensure that a Quality...  ...aerospace fields with experience in FDA regulatory requirements, ISO 13485, and... 

    VulcanForms Inc.

    Harvard, MA
    3 days ago
  • $44k - $185k

     ...TeamThe ASIC Group works closely with other development teams within Cisco, including marketing, system hardware, software, product engineering, and manufacturing. Through this collaboration, members of our group play a major role in the process of defining, developing and... 
    Full time
    Temporary work
    Apprenticeship
    Internship
    Local area
    Flexible hours

    CISCO Systems

    Maynard, MA
    2 days ago
  •  ...timePosted: 2026-10-12The Principal Post Market Quality Engineer serves as the senior technical...  ...trending.Deep knowledge of medical device regulations and quality system requirements,...  ...requirementsMDSAPStrong understanding of FDA, Notified Body, and MDSAP inspection expectations... 

    Hologic

    Marlborough, MA
    2 days ago
  •  ...things and do things right Support all Quality activities of a high-volume...  ...to perform work which involves general engineering methods and tools. As an entry level engineer...  ..., U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures... 
    Immediate start
    Worldwide

    Integer Holdings Corporation

    Hudson, MA
    2 days ago
  • $100k - $120k

     ...Our client is currently seeking a Post-Market Surveillance Quality Engineer to support the ongoing monitoring, safety, quality, and performance...  ...experience. ~ Strong understanding of medical device regulations and post-market surveillance requirements. ~ Experience... 

    Judge Group, Inc.

    Marlborough, MA
    1 day ago
  •  ...Quality Engineer II Pramand, LLC, is a medical device company based in Bedford, MA. We develop...  ...procedures and external standards and regulations, including cGMP, ISO 13485 and 21CFR...  ...functional team setting. ~ Understanding of FDA QMSR and/or ISO 13485 requirements.... 
    Work experience placement
    Worldwide

    Pramand

    Bedford, MA
    2 days ago
  • $130k - $150k

     ...is responsible for leading the Supplier Quality Engineering function and driving the technical...  ...related technical engineering role within a regulated industry. Previous people leadership...  ...Working knowledge of ISO 13485, MDSAP, FDA Quality System Regulation, and supplier... 
    Hourly pay
    Work at office
    Monday to Friday
    Flexible hours

    Nova Biomedical

    Waltham, MA
    26 days ago
  • $90k - $135k

     ...Quality Engineer We're seeking a proactive and detail-oriented Quality Engineer to ensure that our product development...  .... Ensure compliance with applicable standards and regulations, including ISO 13485, FDA 21 CFR Part 820, and EU MDR. Lead and support design... 
    Full time
    Contract work
    Local area

    Convergent Dental

    Waltham, MA
    3 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Quality Engineer - FDA Regulated, Up to $120K (01754). Be the first to apply!