• Senior Director, Portfolio Management, Oncology

    Danaher Corporation (New York, NY)
    …product development through a stage gate process and applicable knowledge of US FDA and International regulations. + Experience working in a corporate, global or ... regional marketing role involving diagnostic or medical device products/services. + Exposure to P&L responsibility, and the related financial acumen needed to drive business decisions and outcomes. + Demonstrated exceptional interpersonal and communication… more
    Danaher Corporation (01/14/26)
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  • Chief Engineer

    ManpowerGroup (Milpitas, CA)
    …facilities management experience, with at least 5 years in pharmaceutical or FDA -regulated environments. + HVAC certification such as NATE or equivalent, and ... electrical licensing or certification. + Experience with validated systems, GMP, GLP, and GCP regulations. + Proven leadership skills managing multidisciplinary teams and vendor relationships. **What's in it for me?** + Opportunity to work in a critical role… more
    ManpowerGroup (01/14/26)
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  • Full-Time Plasma Center Nurse (EMT-P, LPN or RN)

    BioLife Plasma Services (Snellville, GA)
    …(in state of licensure) for basic IV therapy Satisfactorily complete the FDA approved training requirements for BioLife Medical Support Specialist Two years in ... a clinical or hospital setting **What Takeda can offer you: ** Every day at Takeda, we feel good knowing that what we do helps improve the lives of patients with rare diseases. At BioLife, while you focus on our donors, we will support you. We offer a purpose… more
    BioLife Plasma Services (01/14/26)
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  • International Shipping Material Handler

    ADM (Erlanger, KY)
    …to ensure that all rules and regulations set forth by the US Customs & FDA are in place and being followed in regards to compliance related activates. Additionally ... responsible for researching and implementing processes as required to meet all company and departmental goals and objectives. To ensure global supply chain is minimally affected and be proactive with identifying risk to the supply chain. **Responsibilities and… more
    ADM (01/14/26)
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  • Document Control Specialist I

    Cordis (Irvine, CA)
    …Proficiency in MS Office applications (Word, Excel, Outlook). + Knowledge of ISO 13485, FDA 21 CFR Part 820, or similar quality system standards. + Fluent in English ... **Preferred Qualifications:** + 3+ years of document and change control experience in the regulated environment. + 3+ years of relevant experience in the Medical Device Industry. **Key Competencies** + Precise, rigorous, and detail-oriented approach to… more
    Cordis (01/14/26)
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  • Senior/Medical Science Liaison - Advanced Lung…

    United Therapeutics (UT)
    …their daughter's pulmonary arterial hypertension (PAH). Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial ... lung disease (PH-ILD) and neuroblastoma, a rare pediatric cancer. Our near-term pipeline seeks to develop additional therapies for PAH and pulmonary fibrosis (PF). The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an… more
    United Therapeutics (01/14/26)
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  • Production Supervisor

    ZOLL Medical Corporation (Pittsburgh, PA)
    …Super Saturated Oxygen (SSO2) Therapy is the first FDA -approved therapy since the stent 20+ years ago to ... reduce infarct size in patients with the most severe heart attacks. Heart disease is the leading cause of death for both men and women in the US At ZOLL, your work will help to ensure cardiac patients get the life-saving therapy they need. ZOLL has been… more
    ZOLL Medical Corporation (01/14/26)
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  • Process Development Engineer

    3D Systems, Inc. (Rock Hill, SC)
    …manufacturing operations, preferably in the medical device industry under FDA /ISO 13485 design controls. Candidates should be comfortable working in ... the methodical, structured, and well-documented manner expected in a highly-regulated industry. Solid understanding and background in core manufacturing engineering fundamentals, such as process development, light design work, data analysis, statistics,… more
    3D Systems, Inc. (01/14/26)
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  • Supervisor, Quality & Reliability Engineering

    TE Connectivity (Medway, MA)
    …environment. * Prior management/supervisor experienced preferred * Working knowledge of FDA /ISO/MDD Quality systems for medical device companies. * Excellent written ... and oral communication skills essential **Competencies** Values: Integrity, Accountability, Inclusion, Innovation, Teamwork **ABOUT TE CONNECTIVITY** TE Connectivity is a global industrial technology leader creating a safer, sustainable, productive, and… more
    TE Connectivity (01/14/26)
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  • Intern - Procurement

    United Therapeutics (Research Triangle Park, NC)
    …their daughter's pulmonary arterial hypertension (PAH). Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial ... lung disease (PH-ILD) and neuroblastoma, a rare pediatric cancer. Our near-term pipeline seeks to develop additional therapies for PAH and pulmonary fibrosis (PF). The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an… more
    United Therapeutics (01/14/26)
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