- 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
- 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
- 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
- Sanofi Group (Bridgewater, NJ)
- …entity, provide input to the clinical development plan, work on the development of the clinical trial protocol , clinical trial materials, and take ... **Job Title:** Development Scientific Director **Location:** Cambridge, MA **About the...to clinical study report in compliance with quality and regulatory processes. We are an innovative global healthcare company… more
- Penn Medicine (Plainsboro, NJ)
- …trial budgets. Communicating any specialized study budget needs to the budget specialist , including any changes necessitated by a protocol modification and ... study management from start to finish working closely with the CRU Regulatory coordinators to manage, review, and initiate trials to ensure competitive activation… more
- Hackensack Meridian Health (Edison, 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 ... research nurses and regulatory specialists on all regulatory issues and changes within the protocol ....for study equipment and supplies. + Participates in the development of study protocols including guidelines for administration or… more
- Bristol Myers Squibb (New Brunswick, 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 (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