2,022 Results for

Quality Specialist Jobs in Burlington, MA

Jobs

Weymouth, MA

Continuous improvement practices throughout manufacturing process and assisting departments with quality inspections or oversight as needed. We are looking for an eager and motivated individual for a great opportunity to learn and grow long term!

5 days ago

Beverly, MA

$55,000–$65,000 / year
Full time

This position works closely with Engineering, Manufacturing, Operations, and Quality teams to ensure documentation, training records, regulatory requirements, and quality processes remain accurate, compliant, and audit-ready. We are seeking a Document Control & Regulatory Compliance Specialist to play a key role in maintaining and improving our Quality Management System (QMS).

10 days ago

Lowell, MA

$55,000–$62,000 / year
Full time

p>This is a hands-on role where you'll work closely with production, quality, engineering, and HR teams to deliver engaging technical training that helps employees perform at their best. If you enjoy teaching, mentoring, and creating effective training programs in a manufacturing environment, we'd love to hear from you.

7 days ago

Wilmington, MA

$92,500–$171,500 / year

This role will be responsible for full lifecycle Project Engineering support for a range of software and hardware development, assembly, and integration and test efforts to deliver critical space-based remote sensing systems for our customers. Understands how to develop a schedule using Earned Value on a program with $5M-$20M in value and manage a project using the Earned Value Indicators on a DCMA surveilled program (highest rigor applied).

3 days ago

Marlborough, MA

The incumbent will manage a broad portfolio of services including managed facility services, security services and construction services to achieve sustainable cost reductions, mitigate supply chain risk and drive overall business objectives. Purpose StatementAs a core member of the Indirect Sourcing team, the Indirect Sourcing Specialist leads the development and execution of sourcing strategies for assigned categories within Global Facilities that supports worldwide operations.

Today

Bedford, MA

$90,220–$130,000 / year

Support configuration control by processing, tracking, and recommending dispositions for change notices, ecps, deviation/waiver requests, service bulletins, deficiency reports, Airworthiness Directive Notes, and qcps. Provide integrated logistics support, including provisioning, source coding, maintenance data collection, configuration management data, QDR analysis, and identifying alternate sources of supply for DMS/MS issues.

1 day ago

Devens, MA

$43.27–$45.90 / hour

Minimum of 2+ years of experience working in regulated industries such as Biotech, Pharmaceutical, and Medical Devices familiarity supporting benchtop instruments and applications within a GxP compliant manufacturing or laboratory setting. Review and approve validation lifecycle documents as part of CSV activities, supporting the risk assessments, specifications, pre- and post-approval of qualification testing.

8 days ago

Nashua, NH

Administer and manage key business processes for assigned customer accounts, including quotations, sample and prototype coordination, pre-production, production, order management, quality support, and ongoing customer service. Building on over four decades of leadership and experience, Wakefield Thermal designs, manufactures, and sells thermal management products that remove excess heat generated by electronic components.

30+ days ago

Boston, Massachusetts

$63–$63 / hour
Temporary
Full time

This role ensures efficiency, accuracy, and quality of documentation, supports education and training for CDI Specialists, and collaborates with coding and validation managers to improve documentation practices that directly impact key performance indicators. Job Summary We are seeking an experienced CDI Validation Specialist (CDI Team Lead) to oversee, evaluate, and analyze Clinical Documentation Integrity (CDI) functions.

15 days ago

Marlborough, MA

Communication Technology Services (CTS) is one of the largest integrators and managed service providers in the U.S., specializing in the design, installation, and support of Distributed Antenna Systems (DAS), Small Cell, and 4G/5G Private Wireless Networks. We are driven by the desire to solve complex customer problems, the excitement of deploying new technologies, and our dedication to delivering advanced wireless solutions as simple, scalable offerings for our customers.

Today

Hampton, NH

Category:Quality Control, Keywords:Quality Control / Quality Assurance Specialist, Location:Hampton, NH-03842 Fully comprehend using a ruler and basic math skills.

6 days ago

Northborough, MA

At Kristine Romano Law, every conversation you have represents a family making one of the most important decisions of their lives, protecting their legacy, caring for aging loved ones, and creating clarity for the future. If you are someone who can build trust quickly, communicate value clearly, and confidently guide people to a decision that serves them, this is a rare and meaningful opportunity.

Today

Lunenburg, MA

$19.25–$19.25

Learn to repair vehicle glass (in the classroom and hands on) with a focus on the Safelite Way of Fitting under the guidance of experienced technicians and Safelite leaders. • Manage work orders, customer documentation and customer communication through the Safelite handheld Mobile Resource Management (MRM) technology.

22 days ago

Lunenburg, MA

$19.25–$19.25

24 days ago

Nashua, NH

$18–$19.15 / hour

Patient Access Associate Specialist are responsible for assigning accurate MRNs, completing medical necessity / compliance checks, providing proper patient instructions, collecting insurance information, receiving, and processing physician orders, and utilizing an overlay tool while providing excellent customer service as measured by Press Ganey. This role ensures data integrity, regulatory compliance, and a positive patient experience while directly influencing revenue cycle KPIs such as registration accuracy, point-of-service collections, and first-pass claim rates.

3 days ago

Nashua, NH

$18–$19.15 / hour

3 days ago

Hudson, MA

p>The Entwistle Company isseekinga skilled and motivatedContractSpecialist to build a long-term career in our collaborative and innovative environment.

In this role, you’ll help deliver mission-critical components that support U.S. and allied defense, with your skills, creativity, and impact directly contributing to national and global security.

2 days ago

Manchester, NH

Finally, Lehigh Valley Hospital - Cedar Crest, Lehigh Valley Hospital - Muhlenberg, Lehigh Valley Hospital- Hazleton, and Lehigh Valley Hospital - Pocono each received an 'A' grade on the Hospital Safety Grade from The Leapfrog Group in 2020, the highest grade in patient safety. We're a Magnet(tm) Hospital, having been honored five times with the American Nurses Credentialing Center's prestigious distinction for nursing excellence and quality patient outcomes in our Lehigh Valley region.

30+ days ago

Boston, MA

$17.50–$30.20 / hour

Provides excellent customer service, addresses needs of customers in a timely and effective manner and models suggestive selling techniques; answers phones and pages promptly and courteously. All positions must strive to support WFM core values and goals, promote national, regional, and store programs and initiatives, and ensure adherence to all applicable health and safety regulations including Food Safety and regulatory duties required in the department.

2 days ago

Hanscom AFB, MA

$86,246–$175,000
Full time

Our capabilities in cybersecurity, network architecture, reverse engineering, software and hardware development uniquely enable us to support sensitive missions for the U.S. military and federal agency partners. Our workforce includes skilled tradespeople; artificial intelligence, machine learning (AI/ML) experts; engineers; technologists; scientists; logistics experts; and business administration professionals.

30+ days ago

Middleton, MA

$23–$25 / hour
Full time

In this role you will have you will have the opportunity to work outside on beautiful properties in your community, spending extensive field time diagnosing problems and treating properties. Through our comprehensive lawn and tree care, we work hard to make sure our customers have attractive, healthy and cared-for green spaces to enjoy.

5 days ago

Lincoln, MA

$21–$30 / hour
Full time

Team & Collaborative Environment: Join a supportive team that works alongside some of the best trained and equipped professionals in the industry - with a focus on learning, growth, quality, and safety . You bring: • A degree in Arboriculture, Urban Forestry, Horticulture, Plant Science, Plant Pathology, Environmental Sciences, Landscape Management, Turfgrass—or related experience (preferred) .

30+ days ago

Hanover, MA

Full time

A typical day may include: • Collaborating with crew members to perform pruning, removals, cabling, bracing, and other essential tree care tasks. • Team & Collaborative Environment: Work alongside some of the best trained and equipped professionals in the industry, with a strong emphasis on safety, quality, and teamwork.

30+ days ago

$89,530–$108,490 / year

The Senior Field QA Specialist is responsible for reviewing Manufacturing Batch Records (MBRs), performing real time on-the-floor exceptions reviews and logbooks, conducting GMP area walkthroughs, and supporting timely return-to-service (RTS) walkthroughs to confirm that manufacturing areas and equipment are properly cleaned, calibrated, and ready for production use. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

16 days ago

Hopkinton, MA

$71,000–$94,500 / year

The base pay actually offered to the successful candidate will take into account internal equity, work location, and additional factors, including job-related skills, experience, and relevant education or training. We're seeking a passionate, detail-oriented Quality Specialist to drive impactful documentation and administrative support for our established ISO 13485 Quality Management System at our dynamic Hopkinton facility.

30+ days ago

Watertown, MA

$85,000–$200,000 / year

The individual will play a key role in sustaining day-to-day QMS operations, managing the controlled document lifecycle including biennial review programs, driving training compliance across the organization, and supporting quality systems performance monitoring as Kymera advances late-stage development and commercialization. How you'll make an impact: The Manager/Specialist, Quality Systems is responsible for managing the operational infrastructure of Kymera''s Quality Management System, with primary ownership of document control, training program management, and quality systems compliance monitoring.

7 days ago

Boston, Massachusetts

FICERA specifically addresses a key challenge in solid tumor treatment by enabling immune cell penetration into tumors, reducing fibrosis and immunosuppression while reversing TGF--driven resistance mechanisms - ultimately designed to drive the deep, durable responses that may translate into better outcomes and survival for patients. Founded in 2020, we've built a global team of over 100 employees headquartered in Boston, with a clear focus on advancing our lead asset, ficerafusp alfa, or FICERA - a potentially first-in-class bifunctional EGFR-directed antibody combined with a TGF- ligand trap.

6 days ago

Bedford, Massachusetts

$115,000–$140,000 / year
Full time

The Senior Quality Systems Specialist I will be expected to support all activities within the Quality Systems team shown below but will have primary responsibility for maintenance and improvement of at least one of the following: CAPA process – tracking, trending of approved CAPAs, and driving timely/appropriate completion of activities, ensuring root cause analysis, actions, verification of effectiveness are appropriate. Duties may include CAPA, Internal Audits, Supplier Audits, Affiliate Audits, External Documents, Management Review, Procedure development, key metric reporting and other key project support under the supervision of the Quality Systems Manager.

30+ days ago

Milford, MA

$95,300–$116,600 / year

This is achieved through a combination of experience in Quality Systems coupled with education and training in Quality Systems, cGMP, Quality audits, documentation, change control, corrective/preventative action, validation, calibration, review of quality records, quality metrics, failure investigations, and manufacturing and laboratory controls as per cGMPs. Perform disposition of advanced oligonucleotide products for pharmaceutical use including pharmaceutical intermediates, active pharmaceutical ingredients (API), and adjuvants/constituent materials in accordance with approved specifications and procedures including Avecia Enterprise Resource Planning System (SAP) transactions.

30+ days ago

Remote, USA, MA

Remote

$65–$75 / hour

Candidates with experience in biotech or pharmaceutical quality environments who have supported training administration, document management, audit readiness, or validation documentation activities will be especially well suited for this role. Given your recent work drafting roles involving Veeva Vault and regulated clinical operations, this posting keeps the technical detail strong while remaining candidate-friendly for public distribution.

30+ days ago

Wilmington, MA

$56,100–$82,900 / year

Recruiting Company: Textron Systems Primary Location: US-Massachusetts-Wilmington Job Function: Quality Schedule: Full-time Job Level: Individual Contributor Job Type: Experienced Shift: First Shift Travel: Yes, 10 % of the Time Relocation: Unavailable Job Posting: 04/21/2026, 6:34:00 AM Job Number: 341326. This position works closely with Quality Engineering, Operations, Program Management, and Delivery teams to review, validate, and track production data, ensuring product conformance and readiness of the complete record and data package for customer delivery.

30+ days ago

Marlborough, MA

Qualifications: • Required qualifications: Bachelor's degree in Life Sciences, Engineering, or a related field • Minimum of 8 years experience in Clinical Quality Systems, Clinical Operations/Project Management, or Regulatory Affairs • Medical device industry experience required • Extensive knowledge of FDA, ISO, EU MDR, and medical device quality requirements governing human subject research • Excellent organizational, execution, and communication skills. The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role.

30+ days ago

$34,799–$82,938 / year

p>COMBINATION OF EXPERIENCE AND EDUCATION:

Combinations of successfully completed post-high school education and experience may be used to meet total qualification requirements for the broadband levels specified in the table, and may be computed by first determining the applicants total qualifying experience as a percentage of the experience required for the grade level; then determining the applicants education as a percentage of the education required for the broadband level; and then adding the two percentages.

General Experience : Experience in fields such as quality control, quality inspection, contracting and purchasing, supply and storage, industrial or production planning, research and engineering, maintenance, and test and evaluation that provided (1) familiarity with quality assurance or related work, (2) pertinent product or process knowledge and skill, (3) ability to interpret and apply contract requirements and engineering specifications, and (4) skill in dealing with others in person-to-person work relationships.

30+ days ago

Cambridge, Massachusetts

The QA Specialist will have oversight of and involvement in, GMP compliance for production of Clinical Trial Material (CTM), including work performed by Contract Manufacturing Organizations (CMOs). Participate with Manufacturing Sciences and Clinical Operations in investigations of deviations ensuring the development of Corrective Actions and Preventative Actions (CAPA), as necessary.

1 day ago

Boston, MA

Provides QA support in the management of SCARs assisting in determining impact to incoming raw materials and consumables as well as supporting vendor investigations. 5 years of relevant industry experience such as materials management, supply chain, quality assurance and/or manufacturing in biotechnology/regulated pharmaceutical environment.

30+ days ago

Billerica, MA

$77,000–$86,000 / year

This role works cross-functionally to maintain an inspection-ready QMS, ensure compliance with regulatory and quality requirements, support implementation of external requirements, and drive continuous improvement initiatives that enhance overall quality system performance and operational effectiveness. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, were building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity.

6 days ago

Woburn, MA

Verify that study documentation (e.g., batch records, raw data, final reports) meets regulatory requirements for data integrity, traceability, and transparency. We are seeking an experienced, detail-oriented, and proactive Quality Assurance (QA) Specialist or Manager with a strong background in auditing regulated bioanalytical LC-MS/MS and ELISA studies.

30+ days ago

Bedford, MA

The Senior Specialist, Product Disposition will support the timely and compliant disposition of all the company Gene Therapy products across all stages of manufacturing. The Senior Specialist will bring strong attention to detail, a quality-first mindset, and the ability to work cross-functionally in a fast-paced, regulated environment.

30+ days ago

Boston, MA

Remote

This individual will be responsible for executing test plans, validating configuration changes, documenting defects, and ensuring system functionality meets business requirements. We are seeking a QA Analyst to support testing efforts related to claims configuration, benefit setup, pricing, and adjudication within a healthcare payer environment.

23 days ago

Waltham, Massachusetts

The Senior Specialist will help continuously improve Quality System Procedures related to GMP activities related to their function and will collaborate closely with internal cross-functional teams. The Senior Specialist will perform review of drug substance/drug product manufacturing records and associated documents (i.e. deviations) for product that will be released for use in Kailera phase I-III clinical programs.

21 days ago

Boston, MA

30+ days ago

Somerville, MA

Remote

$63,648–$90,750.40 / year

Qualifications Education Bachelor's Degree required (experience can be substituted in lieu of degree); Master's Degree preferred Experience At least 2-3 years of experience in a CMS STARs role, specializing in STARs program execution required At least 2-3 years experience managing STARs data, data validation, and outcomes required. Additional Job Details (if applicable) Working Conditions * This is a remote role that can be done from most US states Remote Type Remote Work Location 399 Revolution Drive Scheduled Weekly Hours 40 Employee Type Regular Work Shift Day (United States of America) Pay Range $63,648.00 - $90,750.40/Annual

30+ days ago

Watertown, MA

$109,150–$126,850 / year

This position provides QA oversight to daily operations, supports batch review and release, manages deviations and CAPAs, and partners closely with manufacturing, QC, manufacturing sciences & technology, and radiological safety teams to maintain a robust, inspection-ready quality culture. Experience with working in and implementing a global QMS adhering to EU GMP Vol 4 Part I, IV, and applicable EU GMP Annexes (including but not limited to Annex 1 and Annex 3), 21 CFR 210-212, 21CFR Part 11, ICH, and USP requirements.

30+ days ago

Cambridge, MA

The Senior Operational Area Quality Specialist - Operational Quality, Materials Management will provide QA support for materials management including the release of incoming raw materials and consumables for internal manufacturing programs at VCGT. This role will support both commercial and clinical manufacturing operations including review of incoming raw data, GMP documentation, QC release testing results and other quality systems documentation as needed in support of materials management.

30+ days ago

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Quality Specialist Jobs in Burlington, MA

Quality Specialist Micro Tech

Documentation Control Specialist EDA Staffing

Training Specialist EDA Staffing

Specialist, Project Engineering (Space Systems) : Sign-on bonus ($15K max) L3Harris Technologies

Indirect Sourcing Specialist – Facilities/ Global Operations # 26-15153 US Tech Solutions, Inc.

Equipment Specialist, Senior - Secret DCS Corporation

TECH SVCS - IT Lab Computing Support Specialist ECLARO

Customer Support Specialist Wakefield Thermal Solutions, Inc.

CDI Validation Specialist Compunnel, Inc.

Data Collection Specialist Communication Technology Services (CTS)

Quality Assurance Express Employment Professionals

Client Engagement & Sales Specialist Kristine Romano Law

Peak Seasonal Repair Specialist Safelite

Seasonal Repair Specialist Safelite

Patient Access Associate Specialist - PRN Ensemble Health Partners

Patient Access Associate Specialist - Part-time Ensemble Health Partners

CONTRACT SPECIALIST The Entwistle Company

Child Life Specialist - FT Days - Pediatrics and PICU - Weare Lehigh Valley Health Network

Inventory Specialist Whole Foods Market

Cybersecurity Assessment and Authorization (A&A) Specialist Company Confidential

Aeration Specialist SavATree

Plant Health Care Specialist SavATree

Ground Operations Specialist SavATree

Senior Specialist, Field Quality QA Operations Bristol-Myers Squibb Co

Quality Systems Specialist Revvity Inc

Specialist/Manager, Quality Systems Kymera Therapeutics Inc

Sr. Quality Specialist, GxP Document Control Bicara Therapeutics

Senior Quality Systems Specialist I Werfen

Senior Quality Assurance Specialist, PPQ/Commercial QA Projects Nitto Denko Avecia Inc

Senior Quality Systems Specialist Connexion Systems + Engineering

Quality Specialist Textron Inc

Principal Specialist, Corporate Clinical Quality Assurance Boston Scientific Corp

QUALITY ASSURANCE SPECIALIST - DIRECT HIRE AUTHORITY United States Air Force

Quality Assurance Specialist Voyager Therapeutics

Sr. Quality Specialist, Material Management Katalyst Healthcares & Life Sciences

Quality Assurance Specialist Nova Biomedical Corp

Quality Assurance Specialist/Manager – Bioanalytical Laboratory Novabioassays LLC

Product Disposition Sr. Specialist, Quality The Steely Group

QA Specialist- REMOTE Sierra Solutions Group

Senior Specialist, GMP Quality Assurance Kailera Therapeutics

Sr. Quality Specialist, Material Management Karwell Technologies

STARS Quality Specialist Brigham and Women's Hospital

Senior Quality Assurance Specialist, RLT Manufacturing Operations Mariana Oncology Inc

Vendor Quality Management Specialist Expert In Recruitment Solutions

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