75 medical device engineer jobs at 33 companies in New Jersey
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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
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
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.
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.
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).
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.
Maquet: German medical technology manufacturer supplying surgical, cardiovascular, critical-care, and operating-room equipment to hospitals.
5+ YOEMaster's preferred or bachelor's in mechanical/biomedical engineering with 5+ years process development/design transfer in medical device industry; Six Sigma belt, validation and statistical analysis experience, SolidWorks/Creo proficiency.
BDNYSE: BDX: Global medical technology advancing the world of health.
10+ YOEBachelor's degree in engineering and 10 years of engineering and process development experience in regulated manufacturing; medical device experience, capital project leadership, validation, FMEA, Lean, and SPC knowledge required.
Trumbull or Livingston or Stafford or North Tonawanda
OnsiteFull Time
CooperSurgical: Women's Health Innovators
10+ YOE10+ years quality engineering experience in medical devices (8+ with MS). Requires expertise in design controls, risk management (ISO 14971, FMEA), V&V, QMS (21 CFR 820, ISO 13485), and strong communication/project skills.
Microsoft Excel, Microsoft Word, Microsoft PowerPoint, PPAP, FMEA
EPTAM Precision Molding: A precision molding producing medical device components in tightly controlled cleanroom environments.
5+ YOE5+ years injection molding experience in medical device or high-volume molding; knowledge of scientific molding, IQ/OQ/PQ validation, ISO quality systems, and strong communication and troubleshooting skills.
Senior/Principal Engineer or Scientist, Combination Products
Bern or Munich or Switzerland or Research Triangle Park or Boston or Chicago or Philadelphia or New Jersey
HybridFull Time
Kymanox: Life sciences professional services and consulting firm helping pharmaceutical, biotechnology, and medical-device companies develop and commercialize medicines.
8+ YOEMinimum 8+ years in medical device, pharmaceutical, or combination product industries, bachelor's in engineering or science required, subject matter expertise in combination products, technical leadership and client-facing experience.