• Project Engineer, Packaging

    Globus Medical, Inc. (Audubon, PA)
    …Engineering, Packaging Engineering or any related technical discipline + Previous medical device packaging design experience preferred. **Our Values** **:** ... At Globus Medical , we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team… more
    Globus Medical, Inc. (06/25/25)
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  • Marketing Manager, Posterior Interbody Fusion

    Globus Medical, Inc. (Audubon, PA)
    …experience; or equivalent experience + Preferred experience in Product Marketing/Management in the medical device industry + Ability to travel up to 15% of ... At Globus Medical , we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team… more
    Globus Medical, Inc. (07/25/25)
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  • Research Coordinator - Heart Vascular Research…

    WellSpan Health (York, PA)
    …collection of research data for patients in clinical trials. Assists the medical investigators in achieving the objectives of clinical research studies and supports ... based on research study requirements. + Assists investigators in evaluating the quality of care and compliance to protocol requirements. Follows by ensuring… more
    WellSpan Health (07/22/25)
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  • Senior Manager-Corrections & Removals

    Philips (New Kensington, PA)
    …proven functional/strategic leadership of Post Market Surveillance/C&R teams, detailed knowledge in FDA and Global Medical Device regulations, strong ... important role in ensuring Sleep & Respiratory Care product quality and patient safety. **Your role:** + Will Manage...You've acquired a minimum of 8+ years' experience in FDA Regulated Post Market Surveillance (PMS), with a focus… more
    Philips (08/19/25)
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  • Associate Director, Regulatory Affairs

    United Therapeutics (Harrisburg, PA)
    …daughter's pulmonary arterial hypertension( **PAH)** . Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial ... ), livers ( **miroliver(R)** ), and a bioengineered external liver assist device for acute liver failure ( **miroliver** **_ELAP_** **(R)** ), with plans… more
    United Therapeutics (08/10/25)
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  • Process Engineering Manager

    West Pharmaceutical Services (Williamsport, PA)
    …for developing, optimizing, and maintaining robust injection molding processes for medical device manufacturing. This role requires deep technical expertise ... years in a leadership or management role. + Proven experience working in the ** medical device industry** with a strong understanding of regulatory requirements (… more
    West Pharmaceutical Services (07/18/25)
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  • Sr. Systems Engineer

    Omnicell (Pittsburgh, PA)
    …creation and maintenance of documentation, and ensuring compliance with relevant medical device regulations + Other duties include troubleshooting, mentoring, ... field, with prior experience in a leadership role + Strong understanding of medical device design, regulatory processes, system integration, and standards like … more
    Omnicell (08/13/25)
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  • Sr. Engineer, R&D, Integrated Systems

    West Pharmaceutical Services (Exton, PA)
    …Engineering preferred **Work Experience** + Minimum 5 years of experience in the medical device or combination products industry + Expertise with test method ... development, validation strategy, and execution + Expertise in medical device design control and change management + Experience in high-volume, automated… more
    West Pharmaceutical Services (07/04/25)
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  • Business Development Mgr, ESD (East Coast)

    Fujifilm (Harrisburg, PA)
    …United States. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... 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)
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  • Sr Clinical Consultant, MI I

    Fujifilm (Harrisburg, PA)
    …and II + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...Provides on-going support to resolve application related and image quality concerns on both a product and system level.… more
    Fujifilm (08/11/25)
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