• Enrollment Registration Specialist (Higher…

    CUNY (Brooklyn, NY)
    …state and federal rules and regulations; advises College personnel regarding the development and implementation of responses to regulatory changes - Oversees ... Enrollment Registration Specialist (Higher Education Assistant) **POSITION DETAILS** New York...May train faculty and staff on retention techniques, record-keeping protocol and/or registration systems - May supervise office operations… more
    CUNY (10/24/24)
    - Save Job - Related Jobs - Block Source
  • Root Cause Analysis Specialist (Director)

    Pfizer (New York, NY)
    **The Root Cause Analysis Specialist will be responsible to:** + Lead the investigation/root cause analysis, corrective/preventive action (CAPA) plan development ... Case Leads while they obtain RCA Certification. The RCA Specialist will also be a subject matter expert in...teams error proof the process in question. **CAPA Plan Development and Management** Based on identified root causes, the… more
    Pfizer (11/09/24)
    - Save Job - Related Jobs - Block Source
  • Senior Specialist , Quality Assurance Label…

    Bristol Myers Squibb (Summit, NJ)
    …BMS with our Cell Therapy team. The Quality Assurance Label Control Senior Specialist at the S-12 Cell Therapy m anufacturing facility is responsible for supporting ... labels for manufacturing and packaging labeling activities for Cell Therapy Development and Operations (CTDO). **Shift Available:** + Wednesday-Saturday, Onsite, 4… more
    Bristol Myers Squibb (11/09/24)
    - Save Job - Related Jobs - Block Source
  • Clinical Research Coordinator

    Hackensack Meridian Health (Hackensack, NJ)
    …+ Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within the protocol . + In collaboration… more
    Hackensack Meridian Health (10/22/24)
    - Save Job - Related Jobs - Block Source
  • Senior Director, Product Stewardship

    Bristol Myers Squibb (Summit, NJ)
    …Data Sheets (MSDS) for BMS-related materials in line with global regulatory requirements, overseeing Environmental Toxicity management processes, and managing ... regulatory -required chemical registration requirements. The role will also provide...-required chemical registration requirements for materials used in the development and production of BMS products (eg, REACH, TSCA).… more
    Bristol Myers Squibb (11/14/24)
    - Save Job - Related Jobs - Block Source