82 medical device engineer jobs at 41 companies in Clark, NJ
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Sr. Device Engineer
Parsippany, New Jersey, United States
$83k-$138k/yrHybridFull Time
PfizerNYSE: PFE: Multinational pharmaceutical and biotechnology.
2+ YOEBachelor's with 2+ years or Master’s with 0+ years; or Associate’s with 6+ years; high school diploma with 8+ years. Knowledge of device design control, risk management, medical devices, ISO 13485/14971, 21 CFR Part 820; strong problem solving and teamwork.
21 CFR Part 820, ISO 13485, ISO 14971, Design of Experiments, Statistical Process Control, Medical Device Standards
Senior Medical Device Research and Development Engineer
Brooklyn, New York, United States
$100k-$160k/yrOnsiteFull Time
Cresilon: Biotechnology developing hemostatic medical devices for veterinary, trauma, and biosurgery users.
5+ YOEBS in engineering or related field required, 5+ years product development experience (4+ in cGMP R&D), hands-on medical device R&D, FDA/ISO knowledge, SolidWorks and Microsoft Office proficiency, strong leadership and experiment design skills.
SolidWorks, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
Integra LifeSciencesNasdaq: IART: Global leader in regenerative technologies and neurosurgical solutions.
5+ YOEBachelor’s in engineering, life sciences, biostatistics, data analytics; 5–8 years in medical device quality or analytics; expertise in complaint trending and regulatory guidelines.
Statistical software, Data visualization tools, Microsoft Office
Compass Group USALondon Stock Exchange: CPG: Leading provider of food and support services.
2+ YOEBachelor's degree in IT or Biomedical Engineering, 2+ years in healthcare technology, IT, or cybersecurity, medical equipment experience, CMMS knowledge, and CompTIA A+/Network+ required.
Computerized Maintenance Management Systems (CMMS), DICOM, HL7
ZOLL Medical: Global developer of medical devices and software for emergency care.
15+ YOE7+ MgmtAdvanced engineering degree and 15+ years developing electronic hardware and embedded software for real-time medical instruments; 10+ years systems engineering; 7+ years leading systems engineering; knowledge of FDA/EC regulations and human factors.
real time operating systems, digital signal processing
AbbottNYSE: ABT: Global healthcare technology focused on life-changing medical innovations.
10+ YOE2+ MgmtRequires 10+ years in electrical or electronic engineering, 2+ years of engineering management, regulated medical-device experience, communication skills, and knowledge of GxP, ISO, and medical-device regulations.
Food and Drug Administration (FDA), Ethernet, PCB, GxP, ISO
Quality Systems Manager – Medical Device Manufacturing
Fairfield, New Jersey, United States
OnsiteFull Time
Weiss-Aug MedPharma: Family-owned contract manufacturer serving medical-device, automotive, aerospace, defense, and industrial OEMs with stamped, molded, and assembled components.
10+ YOE10+ years in medical device quality systems; ISO 13485 and FDA QSR experience; manage QMS, audits, and regulatory readiness; Bachelor’s in Engineering or Quality.
Electronic QMS platforms, ISO 13485, FDA QSR, 21 CFR Part 820
GroupA: Technology consulting firm delivering enterprise cloud platforms, IT audits, and AI guidance for commercial and private-equity clients.
1+ YOERequires 1–2 years of pharmaceutical or medical device contractor oversight and an associate, bachelor's, or advanced engineering-related degree. EHS familiarity and strong communication and organizational skills required.
Clarapath: Private U.S. medical robotics automating histopathology workflows for hospitals, laboratories, researchers, and pathology professionals.
3+ YOEBachelor's in electrical engineering, 3+ years product development experience, circuit and PCB design, embedded hardware and test equipment proficiency, troubleshooting, and medical device/regulatory familiarity.
AbbottNYSE: ABT: Global healthcare technology focused on life-changing medical innovations.
Requires 10+ years in electrical or electronic engineering, 2+ years of engineering management, and extensive knowledge of regulated medical device development, GxP, ISO, and safety requirements.
Amneal PharmaceuticalsNASDAQ: AMRX: Developer and manufacturer of generic and specialty pharmaceutical products.
2+ YOEBachelor's in Pharmaceutical/Biomedical Engineering; Master preferred. 2+ years in pharmaceutical/manufacturing. Strong communication; MS Word/Excel/PowerPoint; knowledge of manufacturing equipment; solid oral, medical device processes.
Medical Components, Inc.: Privately held medical-device manufacturer developing vascular-access catheters and accessories for interventional medicine and dialysis.
3+ YOE3-5 years in manufacturing/medical device industry; materials characterization; leadership and collaboration.
SolidWorks, CAD, FEA, Mold flow, ISO 10993, FDA, GMP, GLP
Kashiv BioSciences, LLC: U.S.-based biopharmaceutical developing and manufacturing affordable biosimilars and complex medicines for patients worldwide.
8+ YOEEngineering or pharmaceutical degree and 8+ years in medical device or FDA-regulated environments. Requires validation, quality systems, cGxP, ISO, technical writing, and Microsoft Office experience.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
VB Spine: Family-owned medical technology that manufactures spine implants, surgical instruments, and navigation solutions for surgeons and patients.
4+ YOEBachelors in Mechanical/Biomedical Engineering required (Master's preferred), 4+ years medical device product development experience, proficiency with parametric CAD (Creo or SolidWorks), GD&T, experience with design controls and regulated industry standards (FDA, ISO 13485).
Prestige Consumer HealthcareNYSE: PBH: Public U.S. that develops, manufactures, markets, and distributes over-the-counter consumer healthcare products for consumers.
5+ YOEMS or PhD in biomedical/mechanical engineering or related field; 8+ years post-MS or 5+ years post-PhD industry experience in medical device R&D; expertise in biomechanics, human factors, CFD/FEA, and validation for Class I/II devices.
AbbVieNYSE: ABBV: Global biopharmaceutical discovering and delivering innovative medicines.
3+ YOEBachelor's degree in engineering or a scientific discipline required. Requires technical problem-solving ability; 3 years of pharmaceutical or medical device process engineering experience is highly desirable.
OrganOx: UK-based medical device developing normothermic organ-preservation systems for liver transplantation and organ failure.
2+ YOEBachelor's in Mechanical Engineering, 2+ years mechanical design experience, proficiency in CAD (SolidWorks preferred), experience with design verification/testing, and ability to work in regulated medical device environments.
Proven Recruiting: Recruiting agency connecting employers with finance, accounting, technology, and life-sciences professionals for permanent and contract roles.
10+ YOEBachelor's in mechanical engineering and 10+ years designing, developing, and testing mechanical systems; CAD, SolidWorks PDM, GD&T, FEA, prototyping, medical-device safety, and manufacturing experience required or preferred.
Computer-Aided Design (CAD), SolidWorks PDM, 3D printing, Finite Element Analysis (FEA), Computational Fluid Dynamics (CFD), IEC 60601-1, ISO 10993-1, UL, CE, FDA
Blue Bell or Somerset or Cary or Burlington or Houston or Leawood or Emeryville or Irvine or Germantown or Elkton or Cherry Hill
$67k-$112k/yrFieldFull Time
IPS-Integrated Project Services: Technical consulting, architecture, engineering, and construction management firm.
2+ YOEBachelor of Science in Engineering, 2+ years relevant experience in pharmaceutical/biotech/medical device commissioning/validation/QA, knowledge of cGMP, ability to lift 50 lbs, cleanroom gowning, and travel extensively.
Vantage MedTech: Private medical-device design and manufacturing firm serving medtech startups and large medical-device companies.
10+ YOEBachelor's in Mechanical Engineering required, 10+ years industry experience designing, prototyping and testing mechanical systems for medical devices; SolidWorks/PDM experience, GD&T, FEA/FEM, IEC 60601-1 familiarity, regulatory documentation and leadership experience.