• 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
  • Senior Principal Engineer

    Bristol Myers Squibb (New Brunswick, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . **Drug Product Development (DPD)** Our Drug Product Development team is committed to ... engine of innovation includes unrivaled industry leading expertise in CMC development of small molecules, protein biotherapeutics, protein degraders, and other… more
    Bristol Myers Squibb (11/18/24)
    - Save Job - Related Jobs - Block Source