58 medical device engineer jobs at 28 companies in Brookhaven, PA
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Device Engineer II
West Chester or West Chester
OnsiteFull Time
TevaNYSE: TEVA: Global leader in generic and specialty medicines.
0+ YOEBachelor's degree in mechanical, biomedical, or related engineering; 0–2 years of pharmaceutical, biotech, or medical device experience; lab testing experience and knowledge of engineering principles, protocols, and regulated development.
Waltham or Zebulon or Marietta or Ware or Upper Providence or Barnard Castle or Cambridge or Rockville or San Francisco
$143k-$238k/yrHybridFull Time
GSKLondon Stock Exchange (LSE): GSK: Global biopharmaceutical focused on medicines and vaccines.
10+ YOEBachelor's in engineering or science with 10+ years in medical device manufacturing, or master's with 5+ years; requires GMP, regulatory, ISO, device lifecycle, risk management, and technology transfer expertise.
FDA 21 CFR 820, EU MDR, ISO 13485, ISO 14971, ISO 10993, GMP, ICH Guidelines, FDA QSR, DHF, Technical File, Microsoft Excel
HologicNasdaq: HOLX: Developing medical technology focused on women's health.
5+ YOEExpert in .NET/C# and object-oriented design with strong CS fundamentals, multithreading, debugging, CI/CD and software architecture; 5+ years (Bachelors) or 4+ years (Masters) experience; mentoring and technical leadership skills; medical device experience a plus.
Senior Manager GRA CMC Combination Product and Stand Alone Medical Device Specialist
King of Prussia or Waltham
OnsiteFull Time
CSL Behring: Global biotherapeutics leader driven by our promise to save lives.
Bachelor's degree in engineering, science, or related field required; advanced degree preferred. Requires 5+ years of progressive medical device, pharmaceutical, or biotechnology regulatory experience and global device regulatory expertise.
EU MDR, ISO 13485, ISO 14971, ISO 15223, ISO 10993, IEC 62366, IEC 62304, IEC 60601, ISO 20916, ISO 18113, ISO 23640, 21 CFR Part 820, QSR, BIMO, 513(g), IDE, 510(k), PMA, De Novo 510(k), EMA, PEI, AGES, PMDA, Health Canada
Globus MedicalNYSE: GMED: Innovating musculoskeletal technology to improve patient care.
3+ YOEBachelor's degree in mechanical, bioengineering, biomedical engineering, or similar field; 3+ years of mechanical design engineering experience; CREO or SolidWorks and CAD proficiency; medical device experience preferred.
CREO, SolidWorks, CAD, Microsoft Excel, Microsoft PowerPoint, Microsoft Project
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.
Almac Pharma Services: Privately owned contract pharmaceutical development and manufacturing organization serving global biopharmaceutical companies.
2+ YOETechnical or trade school degree and 2–5 years of engineering maintenance experience in pharmaceutical, medical device, biotech, or food industries; requires controls, equipment, troubleshooting, and electro-pneumatic and hydraulic expertise.
Boehringer Laboratories: Family-owned US medical device manufacturer making clinical suction controls and minimally invasive devices for hospitals and clinicians.
8+ YOEBachelor's in mechanical or biomedical engineering, minimum 8 years medical device engineering experience, SolidWorks/CAD proficiency, knowledge of FDA regulations and ISO 13485, project planning and technical documentation skills.
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.
Spacelabs Healthcare: Medical-equipment manufacturer providing patient monitoring, diagnostic cardiology, and clinical decision-support solutions to hospitals and clinics.
5+ YOEAssociate degree or equivalent technical training, 5+ years of field service and complex medical device experience, computer and networking skills, valid driver's license, and ability to travel regionally.
Microsoft Windows, XP, SAP R/3, Microsoft Dynamics CRM, Oracle, Microsoft Word, Microsoft Excel, Microsoft Visio, Microsoft PowerPoint, Spacelabs
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.
Teleflex IncorporatedNYSE: TFX: Global provider of medical technology solutions for healthcare.
2+ YOEBS in Engineering, 2+ years related experience in medical device or regulated industry; familiarity with SolidWorks, SAP, Agile PLM, Minitab; knowledge of design controls, V&V, risk management, IQ/OQ/PQ, DFMEA/UFMEA, CAPA, ISO 13485 and FDA 21 CFR 820.
Spacelabs Healthcare: Medical-equipment manufacturer providing patient monitoring, diagnostic cardiology, and clinical decision-support solutions to hospitals and clinics.
5+ YOEAssociate degree or equivalent technical training, 5+ years of field service and complex medical device experience, computer and networking skills, valid driver's license, good driving record, and ability to travel and lift 50 pounds.
Microsoft Windows, XP, SAP R/3, Microsoft Dynamics CRM, Oracle, Microsoft Word, Microsoft Excel, Microsoft Visio, Microsoft PowerPoint
Senior Manager GRA CMC Combination Product and Stand Alone Medical Device Specialist
King of Prussia or Waltham
OnsiteFull Time
CSL Behring: Global biotherapeutics leader driven by our promise to save lives.
5+ YOEBachelor’s degree in engineering, science, or related field required; advanced degree preferred. Requires 5+ years of progressive regulatory experience and expertise in global medical device and drug development regulations.
FDA, EU MDR, ISO 13485, ISO 14971, ISO 15223, ISO 10993, IEC 62366, IEC 62304, IEC 60601, ISO 20916, ISO 18113, ISO 23640, 21 CFR Part 820, QSR, BIMO, 510(k), De Novo, PMA, 513(g), IDE, EMA, PEI, AGES, PMDA, Health Canada
Philadelphia or Jacksonville or Seattle or Los Angeles or Carlsbad or United States
$35-$38/hrFieldFull Time
IQVIANYSE: IQV: Providing advanced analytics, technology solutions, and clinical research services.
3+ YOEBachelor's degree or technical school in electronics; 3+ years repairing, maintaining, and installing medical diagnostic/device equipment; valid driver's license and personal vehicle; able to lift 70 lbs; must clear hospital credentialing and immunization requirements; strong computer and troubleshooting skills.
GHX (Vendormate), Reptrax, Microsoft Outlook, Microsoft Excel, Microsoft Word, Microsoft OneNote
Terumo Medical Corporation: Medical device manufacturer serving healthcare providers with interventional, infusion, drug-delivery, and healthcare-outcomes solutions.
3+ YOEBS in science/engineering required, 3+ years in regulated industry (medical device/pharma) with knowledge of FDA QSR, ISO 13485, EU MDR and MDSAP; strong analytical, communication, auditing, and MS Office skills.
OlympusTokyo Stock Exchange: 7733: Precision technology for medical and scientific solutions.
10+ YOEBachelor's in engineering, 10+ years product quality experience in medical devices or regulated environment, CAPA and complaint investigation expertise, knowledge of 21 CFR Part 820, ISO 13485, ISO 14971, strong analytical and leadership skills, available for regional/international travel.
PFMEAs, 8D, DMAIC, 21 CFR Part 820, ISO 13485, ISO 14971