Lead Quality Engineer, Medical Devices Regulatory
Becton Dickinson & Co
Becton Dickinson in Franklin Lakes, NJ seeks a Quality Engineer to ensure adherence to regulatory standards and manage quality assurance projects across the product lifecycle. Responsibilities include driving quality excellence, managing team projects, and ensuring compliance with FDA regulations. The ideal candidate has a degree in Engineering and extensive experience in medical device quality systems. A comprehensive benefits package, including health coverage and retirement plans, is offered. #J-18808-Ljbffr
- ...Jersey is seeking a Senior Compliance Engineer. This role involves ensuring that electromechanical medical devices comply with global regulatory, quality, and safety standards throughout... ...lifecycle. Key responsibilities include leading compliance evaluations, interpreting...Regulatory
- ...Getinge is seeking a Senior Compliance Engineer in Wayne, NJ to ensure that Cardiac Assist medical devices meet global regulatory and safety standards. Responsibilities include leading compliance evaluations, supporting product designs, and collaborating with multiple...Regulatory
$80.3k - $95k
...Job Description: PURPOSE – The Quality Engineer ensures quality standards, processes and procedures... .../qualifications (IQ, OQ, PQ) Lead the resolution of quality issues related... ...engineering, product development, or medical device testing, validation, or verification,...SuggestedFull timeContract workWork at office- Job Summary: Quality Engineer with mandatory experience in the medical devices domain responsible for planning and executing validation... ...client and project team. Lead and support design verification... ...ISO 13485, and other relevant regulatory standards. Collaborate with...Regulatory
$110.2k - $176.4k
...Responsibilities Drive Quality Excellence: Apply advanced... ...to ensure our medical devices exceed industry standards and regulatory expectations. Solve Complex... ...development and sustaining engineering teams, bringing your... ...manufacturing practices. Lead Project Quality: Ensure...RegulatoryDaily paidTemporary workWork at officeLocal areaRemote workFlexible hours- ...multi-functional team member establishing quality requirements and providing guidance for sustaining engineering projects. Lead or support Risk Management evaluations for... ...candidate will ensure quality standards and regulatory compliance in line with corporate policies,...Regulatory
- ...on delivering only the best quality talent, the first time and every... ...further. Job Title: Quality Engineer (Non-Light Industrial)... ...years of experience in the Medical Device/Biotechnology Industry. Professional... ..., software lifecycle, regulatory requirements, standards, and...RegulatoryImmediate start
$150k - $200k
.... This role exists to ensure that quality enables that mission rather than constrains... ...who will operate as the Quality Lead’s right hand—executing tactically... ...in safety, technical rigor, and regulatory intent Build credibility with engineers, operators, and leadership...RegulatoryLocal areaNight shiftWeekend work- ...Creative Solutions Services, LLC is seeking a Quality Engineer with essential experience in the medical devices sector. You will plan and execute validation activities according to ISO 13485 and ISO 14971 standards while overseeing daily project operations at the client...
$93.2k - $155.4k
A medical technology company is seeking a Senior Engineer for their Joint Replacement Division to support new product development. This hybrid role in Mahwah, NJ involves designing and verifying medical device components, creating engineering documentation, and collaborating...- Kelly Science, Engineering, Technology & Telecom is looking for a highly motivated Senior Engineer in Mahwah, NJ. This role involves... ..., with 2+ years' experience in modeling & simulation in the medical device sector. Preferred qualifications include advanced degrees and...
- ...of the largest global medical technology companies in... ...of us—from design and engineering to the manufacturing... ...Program Overview: BD’s Quality Rotational Program... ...Manufacturing, R&D, Regulatory Affairs, and Medical Affairs... ...BD and in the medical device industry to advance...RegulatoryHourly payRotational programFull timeInternshipWork at officeRemote workRelocationWork visaRelocation packageShift work
- A global medical technology corporation is seeking a Product Development Engineer II for a contract role in Franklin Lakes, NJ. The engineer... ...maintaining compliance with quality standards. Candidates should... ..., specifically in medical devices. Proficiency in Minitab and SolidWorks...Contract work
- ...A leading medical technology company is seeking a Sr. Quality Engineer in Wayne, NJ. This role involves overseeing the quality of... ..., maintaining compliance with regulatory standards, and leading continuous... ..., especially in the medical device sector. Key qualifications...RegulatoryWork from home
- ...Program Overview BD’s Quality Rotational Program offers recent graduates a dynamic... ...:New Product Development,Sustaining Engineering,Manufacturing Quality,Post‑Market... ...teams, including Manufacturing, R&D, Regulatory Affairs, and Medical Affairs. Participate in design, development...RegulatoryRotational programFull timeInternshipRelocationVisa sponsorshipRelocation package
$50k - $60k
...Title Quality Systems Engineer Reports to Quality Systems Manager Department Quality Assurance... ...Annual Drug Reviews and Device History Reviews. Maintains regulatory documents and all documents of external... ...in Pharma, Cosmetics, food, medical device, or allied profession preferred...RegulatoryFull timeWork at officeImmediate start- ...Clinical Development Engineer (Medidata Rave / Technical Support) We are seeking a Clinical Development Support Engineer with deep... ...environments. Familiarity with GxP, 21 CFR Part 11, and other regulatory frameworks. Exposure to cloud platforms and integration...Regulatory
- Stryker Corporation is seeking a Staff Regulatory Affairs Specialist in Mahwah, NJ. This role... ...regulatory compliance, monitor global device regulations, and prepare regulatory submissions... ...and experience with Class II/III medical devices. The position offers a hybrid work...Regulatory
$115k
Sr. Quality Engineer, Quality Operations - Wayne, NJ Location... ...ensuring compliance with regulatory requirements, and... ...improvement. Participate/ Lead validation and... ...Transfer activities the Device Master Records (DMRs)... ...Engineering. Experience in a medical device or...RegulatoryTemporary workWork at officeRemote workWork from homeFlexible hours$114.8k - $191.4k
Stryker Group is hiring a Staff Regulatory Affairs Specialist in Mahwah, NJ to ensure regulatory... ...will have a Bachelor’s degree in Engineering or Science and over 4 years of... ...FDA-regulated environment, ideally with medical devices. The position offers a competitive salary...Regulatory$45 - $55 per hour
A leading staffing firm is seeking a Document/Change Management Specialist in... ...and ensuring compliance with regulatory requirements for medical devices. Candidates should have a BS in a... ...consideration. #J-18808-Ljbffr Kelly Science, Engineering, Technology & TelecomRegulatoryHourly payImmediate start- Stryker is looking for a Staff Regulatory Affairs Specialist in Mahwah, NJ. You will ensure market access and regulatory compliance for... ...with global affiliates. Health and financial benefits include medical insurance, a 401(k) plan, and more, reflecting Stryker's commitment...RegulatoryWorldwide
- Becton Dickinson is seeking a Regulatory Affairs Specialist, Digitalization to manage regulatory documentation and improve digital platforms... ...relevant field and has at least 3 years of experience in the Medical Device industry. This role involves collaborating across teams to...Regulatory
- ...Experience using measurement devices like pin gauges, go-nogo... ...Experience working in a medical device manufacturing... ...reading mechanical engineering drawings and specifications... ...Corporate and Divisional Quality systems and comply with all regulatory and safety guidelines....RegulatoryContract work
- BD is seeking a Regulatory Affairs Strategist, Globalization, to guide worldwide regulatory affairs strategies in Franklin Lakes, New... ...Bachelor’s degree with at least 8 years of experience in the medical device industry, including 5 years in Regulatory Affairs. Key benefits...RegulatoryWorldwide
- BD is seeking a Regulatory Affairs Strategist in Franklin Lakes, NJ. This role involves project management and optimizing... ...field and at least 8 years of experience in Regulatory and Quality, focusing on medical devices. Benefits include competitive salary, bonuses, and...Regulatory
$125k - $150k
A leading medical technology company in Wayne, NJ, is seeking a Staff Human Factors Engineer to lead usability engineering for cardiovascular surgical devices. This role encompasses both front-end innovation and back-end validation to ensure products are intuitive and...- ...Hours/week : 40.00 1st Shift Client : Medical Devices Company Job Category : Professional... ...internal and external customers. Lead communication between, regional business... ...availability, product information, and regulatory issues. Act as the main point of contact...RegulatoryContract workDay shift
- The Quality Control Supervisor is responsible for ensuring the effectiveness of the Quality Management System... ..., internal specifications, and applicable regulatory requirements. The Quality Control Supervisor leads inspection and testing activities, manages quality...RegulatoryWork at office
$120k - $135k
A leading medical technology company is seeking a skilled engineer to provide technical leadership in manufacturing processes. The role includes designing for manufacturability, validation processes, and continuous improvement methodologies. The ideal candidate will have...Remote job
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