US Browse · Boston · Quality Engineer
Quality Engineer in Boston
Honeywell International
Sr Supplier Quality Engineer
Supplier quality engineeringRoot cause analysisCorrective actions~$79,000 – $145,200 py
WORKOPIA ESTIMATEDrive supplier performance improvement initiatives to achieve world-class levels of quality
Woburn, MA, USOn-site+5y experienceJob Match ScoreCreate Profile4 days agoBeckettcottingham
Associate Quality Engineer
Root cause analysisCapa experienceValidation processes$83,500.00 - $133,500.00 usd annual py
Design and conduct comprehensive Quality Engineering studies to identify root causes of quality non-conformances
Woburn, MA, USFully remoteFull time+1y experienceJob Match ScoreCreate Profile10 days agoBDX
Associate Quality Engineer
Root cause analysisCapa experienceValidation processes$83,500.00 - $133,500.00 usd annual py
BDX is seeking an Associate Quality Engineer in Woburn, MA to enhance quality processes in their medical technology division. The role requires a Bachelor’s degree in Engineering and at least one year of quality engineering experience, focusing on problem-solving and continuous improvement in a regulated environment
Woburn, MA, USFully remoteFull time+1y experienceJob Match ScoreCreate Profile11 days agoJninternationalllc
Sr Manufacturing Quality Engineer
Quality system regulationsNon-conformance investigationsProcess validation$79,000.00 - $127,650.00 py
Jninternationalllc looks for a +4y experience Sr Manufacturing Quality Engineer
Danvers, Massachusetts, USFull time+4y experienceJob Match ScoreCreate Profile12 days agoFibrogen
Associate Iii, Quality Technical Product Complaints
Gmp complianceProduct complaint processingCross-functional collaboration$73,000.00-$95,000.00 py
This role is critical in ensuring the timely and compliant processing of product complaints across Biogen's global markets
Cambridge, MA, USFull time+2y experienceJob Match ScoreCreate Profile13 days agoJohnson & Johnson UK
Sr Manufacturing Quality Engineer
Quality system regulationsNon-conformance investigationsProcess validation$79,000.00 - $127,650.00 py
Support the development and manufacturing of life-saving medical devices
Danvers, Massachusetts, USOnsiteFull time+4y experienceJob Match ScoreCreate Profile13 days agoHi Tech IT - An Initiative to Digitise
Associate Quality Engineer
Root cause analysisProcess improvementValidation processes$83,500.00 - $133,500.00 usd annual py
Design and conduct comprehensive Quality Engineering studies to identify root causes of quality non-conformances
Woburn, MA, USFully remoteFull time+1y experienceJob Match ScoreCreate Profile13 days agoBecton Dickinson and Co
Associate Quality Engineer
Root cause analysisProcess improvementValidation processes$83,500.00 - $133,500.00 usd annual py
Design and conduct comprehensive Quality Engineering studies to identify root causes of quality non-conformances
Woburn, MA, USFull time+1y experienceJob Match ScoreCreate Profile14 days agoBecton Dickinson (BD)
Associate Quality Engineer
Root cause analysisProcess improvementValidation processes$83,500.00 - $133,500.00 usd annual py
** Becton Dickinson (BD) is seeking an Associate Quality Engineer for its Woburn, MA location, focusing on quality engineering studies and process improvements in a regulated medical device manufacturing environment. The ideal candidate will have a Bachelor's in Engineering, at least one year of experience in quality engineering, and familiarity with FDA regulations and ISO standards. **
Woburn, MA, USFull time+1y experienceJob Match ScoreCreate Profile14 days agoJohnson & Johnson
Senior Validation Engineer
Bachelor's degree in engineering7+ years process validation experienceKnowledge of tmv and csv protocols$94,000 - $151,800 py
The role involves leading validation efforts for new manufacturing processes to ensure consistency with regulatory standards in the cardiovascular sector
Danvers, Massachusetts, USFull time+7y experienceJob Match ScoreCreate Profile15 days agoJohnson & Johnson / Abiomed
Sr Manufacturing Quality Engineer
2-4 years medical device qa/qe experienceFda qsrs iso13485 iso14971 knowledgeRoot cause investigation and capa expertise$79,000.00 - $127,650.00 py
This role supports the expansion of manufacturing facilities for life-saving medical devices at Abiomed, a Johnson & Johnson company
Danvers, Massachusetts, USOnsiteFull time+4y experienceJob Match ScoreCreate Profile15 days agoJohnson & Johnson MedTech
Sr Manufacturing Quality Engineer
2-4 years qa/qe experience in medical device fieldFda qsrs, iso13485, iso14971 compliance knowledgeRoot cause investigation and non-conformance management$79,000.00 - $127,650.00 py
This role supports the expansion of manufacturing facilities for life-saving medical devices at Abiomed, a Johnson & Johnson company
Danvers, Massachusetts, USFull time+4y experienceJob Match ScoreCreate Profile15 days agoSanofi Genzyme
Device - Senior Quality Engineer, Invitro Diagnostics
10+ years ivd quality management experienceEu ivdr and fda 21 cfr part 809/820 expertiseIso 13485 and iso 14971 risk management knowledge$133,500.00 - $192,833.33 py
This senior subject matter expert role ensures the quality, safety, and regulatory compliance of IVD devices across the full product lifecycle from development to commercialization
Cambridge, MA, USNot specifiedFull time+10y experienceJob Match ScoreCreate Profile15 days agoJohnson & Johnson
Senior Principal Quality Engineer – Design Quality & Systems Excellence
12-15+ years medical device experienceElectro-mechanical software product developmentIso 14971 risk management leadership$122,000.00 - $212,750.00 py
This role serves as a technical leader driving design quality excellence across complex electro-mechanical and software-driven medical devices
Danvers, Massachusetts, USFull time+15y experienceJob Match ScoreCreate Profile15 days agoSanofi
Device - Senior Quality Engineer, Invitro Diagnostics
10+ years ivd quality management experienceDeep knowledge of iso 13485 and eu ivdrExpertise in fda 21 cfr part 820/809 regulations$133,500.00 - $192,833.33 py
This senior subject matter expert role ensures the quality, safety, and regulatory compliance of IVD devices across the full product lifecycle from early development through commercialization
Cambridge, MA, USFull time+10y experienceJob Match ScoreCreate Profile16 days agoJohnson & Johnson Innovative Medicine
Senior Validation Engineer
Bachelor's degree in engineering7+ years process validation experienceKnowledge of tmv and csv protocols$94,000 - $151,800 py
The role involves leading validation efforts for new manufacturing processes to ensure consistency with regulatory standards in the cardiovascular sector
Danvers, Massachusetts, USNot specified; likely hybrid or onsite based on the industry and role.Full time+7y experienceJob Match ScoreCreate Profile16 days agoJohnson & Johnson
Senior Software Design Quality Engineer
5+ years medical device industry experienceIec 62304 and iso 14971 compliance knowledgeSamd and simd technical expertise$109,000.00 - $174,800.00 py
This role supports New Product Development and sustaining activities while playing a key part in product risk management and cybersecurity for chronic heart failure treatments
Danvers, Massachusetts, USFull time+5y experienceJob Match ScoreCreate Profile16 days agoBD
Associate Quality Engineer
Bachelor's degree in engineering1 year qe experienceCapa and root cause analysis$83,500.00 - $133,500.00 usd annual py
The role involves designing comprehensive quality engineering studies to identify root causes of non-conformances and drive process improvements
Woburn, MA, USFull time+1y experienceJob Match ScoreCreate Profile16 days agoSanofi
Device - Senior Quality Engineer, Invitro Diagnostics
10+ years ivd quality management experienceDeep knowledge of eu ivdr and fda 21 cfr part 820Expertise in iso 13485 and iso 14971 risk management$133,500.00 - $192,833.33 py
This senior subject matter expert role ensures the quality, safety, and regulatory compliance of IVD devices from early development through commercialization
Cambridge, MA, USFull time+10y experienceJob Match ScoreCreate Profile16 days agoJohnson & Johnson
Senior Software Design Quality Engineer
5+ years medical device experienceIec 62304 compliance expertiseIso 14971 risk management$109,000.00 - $174,800.00 py
This role supports New Product Development and sustaining activities while playing a key part in product risk management and cybersecurity
Danvers, Massachusetts, USHybrid (minimum of 3 days per week in-office)Full time+5y experienceJob Match ScoreCreate Profile16 days agoSyner-G BioPharma Group
Validation Engineer
3-10 years biotech or pharma experienceFda cgmp and fmea knowledgeEquipment and csv validation expertiseMarket competitive
Syner-G is seeking a Validation Engineer to drive overall quality performance and compliance by defining and maintaining the validation program
Boston, USOn-site+10y experienceJob Match ScoreCreate Profile17 days agoProcter & Gamble
Metrology Ogp Programmer
Ogp measuremind programmingOgp zone3 programmingBlueprint reading and gd&t$32.00 - $52.00 ph
The role involves writing and debugging OGP programs to measure critical dimensions based on technical specifications
Boston, MA, USFull timeMid-levelJob Match ScoreCreate Profile18 days agoSanofi
Device - Senior Quality Engineer, Invitro Diagnostics
10+ years ivd quality management experienceDeep knowledge of eu ivdr and fda regulationsExpertise in iso 13485 and iso 14971 standards$133,500.00 - $192,833.33 py
This senior role serves as a strategic quality partner ensuring the safety and regulatory compliance of IVD devices from early development through commercialization
Cambridge, MA, USNot specifiedFull time+10y experienceJob Match ScoreCreate Profile18 days agoJohnson & Johnson
Senior Software Design Quality Engineer
5+ years medical device industry experienceIec 62304 and iso 14971 compliance knowledgeRisk management and sfmea expertise$109,000.00 - $174,800.00 py
This role supports New Product Development and sustaining activities while playing a key part in product risk management and cybersecurity
Danvers, Massachusetts, USFull time+5y experienceJob Match ScoreCreate Profile19 days agoJohnson & Johnson
Quality Systems Engineer
Bachelor's degree in engineering or related fieldThree years experience in regulated quality systemsComprehensive understanding of iso and fda standards$79,000.00 - $127,650.00 py
The successful candidate will develop, implement, and maintain quality management systems to ensure compliance with industry standards
Danvers, Massachusetts, USNot specifiedFull timeExperience requiredJob Match ScoreCreate Profile19 days ago
WORKOPIA ESTIMATE is shown when an employer doesn't disclose pay. It's the typical range (25th–75th percentile) of disclosed salaries for the same role in the same city, adjusted for seniority and refreshed daily — an estimate, not the employer's figure.
