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

Medical Device Quality Engineer - FDA/ISO Compliance (01460)

$100k

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 2 days ago
Similar jobs that could be interesting for youBased on the Medical Device Quality Engineer - FDA/ISO Compliance (01460) in Littleton, MA vacancy
  • $73.1k - $120.2k

     ...Techne seeks a Supplier Quality Engineer to manage supplier...  ...conduct audits, and ensure compliance with regulatory...  ...internal audits for ISO 13485, ISO 9001, MDSAP...  ...regulated manufacturing (Medical Device, IVD, Biotechnology,...  ...cGMP, ISO 13485, and FDA-regulated... 
    Suggested
    Full time

    Bio-Techne

    Devens, MA
    2 days ago
  • SMC Ltd. is seeking a Quality Engineer II to oversee quality engineering across molding and assembly operations. You will work with engineering...  ...strong analytical and leadership skills, experience with ISO 13485 and 21 CFR 820, and hands-on proficiency with metrology... 
    Suggested

    SMC Ltd.

    Ayer, MA
    1 day ago
  •  ...-09-21Abbott in Westford, MA seeks a Quality Assurance Supervisor I to lead a team...  ...fully onsite setting.You will ensure compliance with FDA regulations and QMS/EMS, drive continuous...  ...with 5+ years of supervisory experience in medical devices/pharma.#J-18808-Ljbffr
    Suggested

    Abbott

    Westford, MA
    4 days ago
  • MedAcuity, LLC is seeking a Senior Quality Assurance Engineer to join our MedTech-focused teams. You will...  ...quality documentation, and drive compliance across design and development artifacts...  ...ensure alignment with 21 CFR Part 820, ISO 13485, and ISO 14971, while supporting... 
    Suggested

    MedAcuity

    Westford, MA
    4 days ago
  •  ...This Role Join a growing medical device manufacturer in Littleton...  ...as our next Operations Quality Manager — a role built for...  ...talented team of Quality Engineers and a QC Supervisor,...  ...one of launch. Ensure compliance with FDA QMSR, ISO 13485, and applicable international... 
    Suggested
    Relocation package
    Flexible hours

    Nexusgtalent

    Littleton, MA
    23 days ago
  •  ...Description: The Director of Quality Assurance and...  ...and future US FDA, ISO, ITAR, and other applicable...  ...assure ITAR and EAR compliance and serves as the primary...  ...; partners with engineers and program managers...  ...manufacturing operations in a Medical Device regulated environment... 
    Work at office

    Precision Optics Corporation Inc

    Littleton, MA
    12 days ago
  •  ...Supplier Quality Engineer At JetCool, a Flex company, we're at the forefront of liquid cooling...  ...audits at key suppliers, assuring compliance with JetCool quality standards. Participate...  ...work you provide: Full range of medical, dental, and vision plans Life... 
    Contract work
    Temporary work
    Visa sponsorship
    Flexible hours

    Flextronics

    Littleton, MA
    4 days ago
  • $23 - $38 per hour

     ...Quality InspectorFounded in 2015 to develop the world's first industrially...  ...quality metrics.Support compliance with customer, internal, industry (AS9100, ISO 9001, ISO 13485), and regulatory...  ...troubleshooting.Experience in medical device, aerospace, or defense manufacturing... 
    Hourly pay
    Shift work
    Night shift
    Weekend work

    VulcanForms Inc.

    Devens, MA
    2 days ago
  • $100k - $130k

     ...Job Description Job Title: Quality Engineer Job Description The Quality...  ...(QMS) in alignment with ISO 9001 and other applicable...  ...audits, ensures regulatory compliance, and uses data-driven analysis...  ...may include the following: Medical, dental & vision Critical Illness... 
    Permanent employment
    Temporary work
    Work at office

    Actalent

    Bedford, MA
    1 day ago
  •  ...floor personnel in support of safety, compliance, productivity, quality standards and company policy....  ...per validated processes, to produce medical devices or sub-assemblies. Work with Quality...  ...efficiency. Working knowledge of ISO, FDA, GMP, and OSHA standards. Technical... 
    Full time
    Temporary work
    Work at office
    Shift work

    SMC Medical Manufacturing

    Devens, MA
    26 days ago
  •  ...recognized premium supplier to the medical market with locations...  ...people. Job Summary: The Quality Engineer II is responsible for all areas...  ...the SOPs. To maintain device history records (DHR) & product...  ...maintain microbial record in ISO class-7 & class-8 as per procedure... 
    Contract work
    Work experience placement

    SMC Corporation of America

    Devens, MA
    2 days ago
  • $96k - $132k

     ...sustainability across aerospace, defense, medical, and other essential...  ...by a shared commitment to quality, curiosity, and accountability...  ...aSenior Manufacturing Quality Engineer, you will serve as the technical...  ...).Strong working knowledge of ISO 9001 / ISO 13485 quality systems... 

    VulcanForms

    Devens, MA
    2 days ago
  • $73.1k - $120.2k

     ...Summary: The Supplier Quality Engineer will play a key role...  ..., reliability, and compliance of materials and...  ...verify compliance with ISO 13485, ISO 9001, MDSAP...  ...environment, preferably Medical Device, IVD, Biotechnology,...  ...cGMP, ISO 13485, and FDA-regulated... 
    Full time
    Temporary work
    Internship
    Worldwide
    Flexible hours

    Bio-Techne

    Devens, MA
    2 days ago
  • Quantum Computing Inc. (QCi) is seeking a hands-on Quality Control Engineer I to work on the Bedford manufacturing floor, defining inspection criteria, developing SOPs, and supporting ISO 9001 compliance. This role partners with Operations to ensure on-time delivery and... 

    Quantum Computing Inc.

    Bedford, MA
    3 days ago
  • $75.41k - $103.69k

    Job Purpose As a Quality Systems Engineer, you will be responsible for helping...  ...compliantly. QMS compliance will be met by ensuring...  ...experience working in the medical device or aerospace fields with experience in FDA regulatory requirements, ISO 13485, and/or AS9100/ISO... 

    VulcanForms Inc.

    Harvard, MA
    1 day ago
  •  ...Position Overview: The Quality Technician is a hands...  ...quality assurance of medical devices during early-stage R&...  ...integrity and compliance by performing detailed...  ...Review and interpret engineering drawings,...  ...accordance with GMP and ISO 13485 standards Collaborate... 

    LanceSoft

    Acton, MA
    3 days ago
  • $75.41k - $103.69k

     ...aerospace, defense, medical, and other...  ...shared commitment to quality, curiosity, and accountability...  ...Customer Quality Engineer serves as a key...  ...audits and ensure compliance with applicable...  ...defense, medical device, or another highly...  ...AS9100 and/or ISO 13485 Quality Management... 
    Remote work

    VulcanForms Inc.

    Harvard, MA
    1 day ago
  •  ...improvements, and serves as a strategic advisor to cross‑functional leaders. The ideal candidate has 5+ years in Finance/Accounting with cost accounting in manufacturing, preferably in medical devices, and strong communication and #J-18808-Ljbffr Mevion Medical Systems, Inc

    Mevion Medical Systems, Inc

    Littleton, MA
    3 days ago
  • $96k - $132k

     ...across aerospace, defense, medical, and other essential...  ...a shared commitment to quality, curiosity, and...  ...PurposeAs a Senior NPI Quality Engineer, you will serve as the...  ...quality records including Device Master Records (DMR),...  .... Working knowledge of ISO 9001, AS9100, or ISO 13... 
    Temporary work

    VulcanForms

    Devens, MA
    2 days ago
  •  ...motivated and hands-on Senior Supplier Quality Engineer to play a critical role in driving supplier...  ...actionsExperience working within ISO 9001-compliant environmentsStrong problem...  ...employer 401(k) match​access to competitive medical, dental, vision, life insurance, short-term... 
    Contract work
    Temporary work

    Electric Hydrogen

    Devens, MA
    3 days ago
  •  ...2. Handle general corporate matters and maintain corporate compliance. 3. Draft and negotiate commercial contracts and other legal...  ...laws; international law experience preferred. 6. Technology / medical device industry experience preferred. 7. Manufacturing industry... 
    Work at office
    Flexible hours

    Mevion

    Littleton, MA
    2 days ago
  • $85k - $105k

     ...Quality Engineer The Quality Engineer is responsible for support the development, and maintenance...  ...programs, ensuring alignment with ISO standards, internal Quality Management...  ...production to ensure product safety, regulatory compliance, and robust validation lifecycle... 
    Apprenticeship
    Local area

    Spirax Group

    Devens, MA
    3 days ago
  • $105k - $125k

     ...strong reputation for engineering excellence, operational...  ...The Senior Quality Engineer will provide...  ...procedures. Perform check on compliance regarding requirements...  ...Help to maintain AS-9100-ISO quality system and certification...  ...employees include medical, dental, vision, life... 
    Full time
    Contract work

    AEM

    Harvard, MA
    4 days ago
  • $117.4k - $161.5k

     ...aerospace, defense, medical, and other essential...  ...shared commitment to quality, curiosity, and accountability...  ...a Staff NPI Quality Engineer, you will serve as a...  ...controls to ensure compliance with AS9100, ISO 9001, and ISO 13485...  ..., including GMP, FDA QSR, and ISO 13485.Proficiency... 

    VulcanForms

    Devens, MA
    2 days ago
  • $75k - $100k

     ...Eurofins seeks a Product Safety Engineer to conduct testing and compliance evaluations for electrical and medical devices against international safety standards. The role involves executing test plans, preparing technical documentation, and communicating with clients at... 
    Work experience placement

    Eurofins

    Littleton, MA
    10 days ago
  • $61.3k - $122.7k

     ...products in diagnostics, medical devices, nutritionals and...  ...Software Design Quality Engineer Working at Abbott...  ...regulatory & standards compliance; collaboratively communicating...  ...Drug Administration (FDA) regulations, other...  ...part 820, IEC 62304, ISO 14971, and ISO 13485... 
    For contractors
    Work experience placement
    Shift work

    Abbott

    Westford, MA
    2 days ago
  • $91.7k - $137.53k

     ...Manufacturing and Engineering....  ...regulatory approval of medical devices in both domestic...  ...support to on-going compliance and corporate initiatives...  ...and fitness for quality• Represent Regulatory...  ...and reports for FDA and support other...  ...1 CFR 820, CMDR, ISO 13485, MDD.• Team... 
    Full time
    Work at office

    Insulet Corporation

    Acton, MA
    1 day ago
  • $129.3k - $258.7k

     ...anticipating changes in medical science and technology....  ..., vessel closure devices and peripheral stents....  ...enforcement decisions related to Quality Assurance (QA),...  ...and Drug Administration (FDA) and international regulations...  ..., pharmacology), math, engineering, or medical fields is... 
    Work experience placement
    Worldwide

    Abbott

    Westford, MA
    1 day ago
  • $125k - $150k

     ...solutions to complex engineering problems and...  ...competencies in Medical Devices, Robotics, and Aerospace...  ...The Senior Quality Assurance Engineer...  ...conformance, and compliance as it relates to...  ...21 CFR Part 820, ISO 13485 with particular...  ...knowledge of FDA 21 CFR Part 820,... 
    Full time
    Flexible hours

    MedAcuity

    Westford, MA
    10 days ago
  • $30 per hour

     ...Position Overview:  The Quality Technician is a hands...  ...quality assurance of medical devices during early-stage R&...  ...integrity and compliance by performing detailed...  ...Review and interpret engineering drawings, specifications...  ...with GMP and ISO 13485 standards  Collaborate... 

    Lancesoft INC

    Acton, MA
    5 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Medical Device Quality Engineer - FDA/ISO Compliance (01460). Be the first to apply!