• Director , Supply Chain Clinical Supply…

    Catalent Pharma Solutions (Philadelphia, PA)
    …supply of material. The successful candidate will work closely with Clinical Operations, Quality Assurance, Regulatory Affairs , and the Program Management ... **Job Description** We are seeking a ** Director in** **Clinical Supply Chain** to be part of our Site Leadership Team. This individual will lead the clinical supply… more
    Catalent Pharma Solutions (10/29/25)
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  • Senior Quality Manager

    West Pharmaceutical Services (Williamsport, PA)
    …+ Directs and manages quality control, quality assurance, quality systems, metrology and/or regulatory affairs , personnel, department resources, ... to operational objectives. **Essential Duties and Responsibilities** + Reporting to the Sr. Director , Quality Assurance, the role will play a critical part in… more
    West Pharmaceutical Services (09/30/25)
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  • Clinical Research Quality Specialist B…

    University of Pennsylvania (Philadelphia, PA)
    …wellness programs and resources, and much more. Posted Job Title Clinical Research Quality Specialist B (Department of Office of Clinical Research) Job Profile Title ... Clinical Research Quality Specialist B...School of Medicine and reports directly to the Associate Director , PSOM Office of Clinical Research Compliance. The Clinical… more
    University of Pennsylvania (11/02/25)
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  • Manager, Medical Core Content - CNS

    Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
    …product strategy and scientific messaging. + Collaborate cross-functionally with Medical Affairs , Regulatory , Legal, and Commercial teams to ensure consistency ... a team-level operational role responsible for the development, maintenance, and day-to-day quality assurance of all core scientific and medical content for the… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • Senior Principal Scientist, Clinical Research,…

    Merck (North Wales, PA)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Neuropathic Pain, Neuroscience, Neuroscience Research, Pain Management, Pharmaceutical Development, Regulatory Affairs Compliance, Regulatory Compliance,… more
    Merck (11/19/25)
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  • Medical Safety Specialist II

    Olympus Corporation of the Americas (Center Valley, PA)
    …across Medical & Scientific Affairs as well as Infection Prevention & Control, Quality Affairs & Regulatory Affairs , Research & Development, Legal, ... therapeutic areas. You will report directly to the Senior Director Medical Safety as a member of the global...+ Various standards (GCP, ISO 13485, ISO 14971) + Regulatory filings (FDA IDE, 510K, EU-MDR CERs, SSCP, PMCFs,… more
    Olympus Corporation of the Americas (10/23/25)
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  • Regional Operations Manager, Onc (RN) - Medical…

    UPMC (Pittsburgh, PA)
    …all regulatory agencies. Responsibilities include the management of operations, quality management, regulatory affairs , continuing education, and fiscal ... out functions of department and Network. Prepares periodic reports as necessary + Regulatory Affairs Management A. Ensures all activities are carried out in… more
    UPMC (11/12/25)
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  • Senior Risk Strategy Analyst

    Highmark Health (Pittsburgh, PA)
    …or related field **EXPERIENCE** **Required** + 5 years in Compliance, Quality , Public Policy, Government Affairs , Project Management, Healthcare Operations ... mitigation strategies; (iv) emerging risk evaluation; (v) completion of compliance / regulatory certifications and filings; and (vi) contribution to the annual audit… more
    Highmark Health (11/11/25)
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  • Supervisor Home Modification Specialist

    AmeriHealth Caritas (Philadelphia, PA)
    …in handling satisfaction issues related to Home Modifications and responds to legal, regulatory affairs and OLTL inquiries. + Prepare reports and conduct ... www.amerihealthcaritas.com . **Responsibilities:** Under the supervision of the LTSS Manager/ Director for Utilization Management, this position is responsible for… more
    AmeriHealth Caritas (11/13/25)
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  • Trial Master File (TMF) Specialist Oncology

    Sumitomo Pharma (Harrisburg, PA)
    …ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory requirements. + ... will be responsible for ensuring that SMPA studies have comprehensive and quality Trial Master Files (TMFs) ready for audits and inspections. Partnering with… more
    Sumitomo Pharma (11/05/25)
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