• R&D Project Manager - Transducer Hardware…

    Philips (Reedsville, PA)
    …of professional experience with leading complex new product development projects in medical device regulated environment and proven track record of delivering ... achieving project scope and objectives while balancing schedule, cost, quality to meet product requirements. **Your role:** + Leading... and reliability metrics, risk management, and FMEA in medical device regulated environment. + You have… more
    Philips (07/04/25)
    - Related Jobs
  • Embedded Software Tester

    Insight Global (Murrysville, PA)
    …Software Test Engineer to join a close-knit test team at one of our largest medical device clients. These testers will be responsible for ensuring the quality ... drive streamlined solutions Perform code reviews with focus on quality , FDA standards, compatibility, and security. Analyze test results...21 CFR Part 820, IEC 62304, ISO 13485) for medical device software development is a plus.… more
    Insight Global (08/26/25)
    - Related Jobs
  • Process Engineering Manager

    West Pharmaceutical Services (Williamsport, PA)
    …or management role. + Proven experience working in the ** medical device industry** with a strong understanding of regulatory requirements (FDA, ISO ... for developing, optimizing, and maintaining robust injection molding processes for medical device manufacturing. This role requires deep technical expertise… more
    West Pharmaceutical Services (07/18/25)
    - Related Jobs
  • Technician Manufacturing, 2nd shift- Exton, PA…

    dsm-firmenich (Exton, PA)
    …of biomaterial science and process innovation, and the leading resource for global medical device and pharmaceutical companies. As a strategic partner with an ... manner assuring DSM products are of consistent and high quality . dsm-firmenich Biomedical is the world's unrivaled biomaterials expert...* 0-5 years, entry level or preferably experience in Medical Device manufacturing or related industry. *… more
    dsm-firmenich (08/09/25)
    - Related Jobs
  • Sr Clinical Consultant, MI I

    Fujifilm (Harrisburg, PA)
    …II + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...HCUS's future business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures… more
    Fujifilm (08/11/25)
    - Related Jobs
  • Lead Expert Sourcing (Direct Materials…

    dsm-firmenich (Exton, PA)
    …**)** **Exton, PA** Every second of every day, a patient receives an implantable medical device featuring one of our biomaterials. Our customized solutions and ... and Purchasing roles in various business-to-business environments. + Experience in the Medical Device industry. + Experience with project management. + Proven… more
    dsm-firmenich (06/22/25)
    - Related Jobs
  • Sterile Processing Specialist--Northeast

    Medtronic (Pittsburgh, PA)
    …understanding of regulatory requirements and industry standards governing medical device reprocessing. + Excellent communication, interpersonal, and ... surgical instrumentation. Commitment to upholding the highest standards of safety and quality in medical device reprocessing. + This position is in the east… more
    Medtronic (08/29/25)
    - Related Jobs
  • Documentation Specialist

    Teleflex (Wyomissing, PA)
    …with product lifecycle management required to purchase, manufacture, and distribute medical device products. **Principal Responsibilities** * Serve as Change ... :12631 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to...driven by our purpose to improve the health and quality of people's lives. Through our vision to become… more
    Teleflex (08/19/25)
    - Related Jobs
  • Business Development Mgr, ESD (East Coast)

    Fujifilm (Harrisburg, PA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... with a Master's degree. + Minimum 8 years of medical device industry experience in a clinical...evolving situations and needs + Strong commitment to delivering high- quality work and upholding HCUS values. + Proficiency in… more
    Fujifilm (07/24/25)
    - Related Jobs
  • Sr. MES Opcenter OR Camstar Consultant - Remote

    Cognizant (Harrisburg, PA)
    …cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries Understand the ... program Awareness of Electronic Lot History Records using Camstar Software for Medical Device / Pharma industries Implement and execute the shopfloor transaction… more
    Cognizant (07/18/25)
    - Related Jobs