• Complaint Management Specialist

    ManpowerGroup (Medina, NY)
    …a cGMP related industry or in a clinical setting. + Strong knowledge of the FDA Quality System and Medical Device Reporting regulations (21 CFR 803, 806, ... Complaint Management Specialist, you will be part of the Quality Assurance department supporting the Product Surveillance team. The...execution. + Gain experience in complaint handling and regulatory compliance within the medical device more
    ManpowerGroup (08/26/25)
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  • Principal Field Clinical Engineer- North East

    Medtronic (Manhattan, NY)
    …**Nice to Have (Preferred Qualifications):** + Experience at Medtronic or within the medical device industry + Experience in the management of clinical devices. ... drive healthcare forward and remain a global leader in medical technology and solutions. To learn more about Inclusion...for all ablation procedures at study sites for investigational device studies to guide the physician on the requirements… more
    Medtronic (08/22/25)
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  • eQMS System Administrator

    Rochester Regional Health (Rochester, NY)
    …+ Bachelor's Degree and 1 Year of experience in a laboratory, pharmaceutical, medical device or clinical research organization OR 4 Years' experience in ... of understanding of the key elements related to electronic Quality Management Systems & regulatory compliance requirements...a laboratory, pharmaceutical, medical device or clinical research organization. PREFERRED… more
    Rochester Regional Health (08/12/25)
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  • Director, Clinical Operations

    Bausch + Lomb (Albany, NY)
    …R&D/Project Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and Drug/ Device Safety, and ... provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input...ICH, GCP and B&L SOPs. + Responsible for the quality of all study-related documentation (eg, Trial Master File,… more
    Bausch + Lomb (06/07/25)
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  • Senior Counsel Life Sciences

    Fujifilm (Albany, NY)
    …and advertising regulations and other regulations specific to Life Sciences/Pharma and Medical Device companies. + Perform other duties as assigned. **Required ... corporate law firm and/or in-house legal department, preferably in the Life Sciences/Pharma, Medical Device or health care field. + Solid commercial contract… more
    Fujifilm (08/15/25)
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  • Account Manager - Sustainable Technologies

    Cardinal Health (Albany, NY)
    …future. **Job Summary** The **Account Manager - Sustainable Technologies** covers our medical device reprocessing portfolio. This position, reporting directly to ... Technologies, is expected to meet or exceed goals by advancing high quality medical sustainability solutions utilizing value-based concept support to the… more
    Cardinal Health (06/24/25)
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  • Coordinator, Point of Care Testing - Laboratory…

    Guthrie (Binghamton, NY)
    …with inpatient staff to coordinate: POCT training and proficiency testing, device implementation and upgrades, POCT reagent inventory, health information system and ... POCT web‐based middleware connectivity and quality assurance monitoring of the POCT program. This program...of the POCT program. This program operates under the medical direction of the Laboratory Director or designated pathologist.… more
    Guthrie (08/08/25)
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  • Ambulatory Office Assistant II

    Bassett Healthcare (Oneonta, NY)
    …we serve, and our communities, achieve optimum health and enjoy the best quality of life possible. What you'll do The Ambulatory Office Assistant II serves ... encounters including face-to-face and telephone interactions. Assures that a high quality patient experience takes place by providing administrative and/or clinical… more
    Bassett Healthcare (08/27/25)
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  • Manufacturing Software Validation Engineer

    Adecco US, Inc. (Buffalo, NY)
    …ability. **Knowledge** + Understands regulated type industries + Knowledge of medical device manufacturers and suppliers' knowledge preferred. + World-class ... grandchildren of employees, On-site gym **Job Summary** The Software Quality Engineer ensures the compliance of computerized...1-3 years working in a manufacturing environment in the medical device industry is preferred. If you… more
    Adecco US, Inc. (08/26/25)
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  • Director, Registered Nurse/Certified Risk…

    Ankura (New York, NY)
    …and pharmacy benefit management companies, as well as pharmaceutical and medical device manufacturers. Responsibilities: + Applies clinical experience and ... diligence. We serve as the Independent Review Organization and Quality Monitorship for many clients, and our work product...acumen to client engagements + Knowledgeable with medical record documentation and understand regulatory compliance more
    Ankura (07/22/25)
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