- Ascendis Pharma (Princeton, NJ)
- …grow and develop their skills. Ascendis Pharma is looking to hire a Senior Manager, Contract Operations to join our team. Responsibilities will include implementing ... demonstrating strong leadership, project management, and communication skills. As the Senior Manager, Contracting Operations, you will be responsible for working… more
- Bristol Myers Squibb (Princeton, NJ)
- …needs in US/UK. As a key operational leader, you will report directly to the Senior Director of Master Data Services, ensuring that master data is timely, ... functions to implement and enforce data quality standards, including data validation , cleansing, and enrichment processes including data quality metrics, trends, and… more
- Merck (Rahway, NJ)
- **Job Description** As a Senior Engineer in Device Design and Process Development group, you will be part of our Research & Development team that designs and ... equipment and processes for medical devices/drug delivery systems. Reporting to the Director responsible for this area, you will partake in medical device assembly… more
- SMBC (Jersey City, NJ)
- …in ALM/IRRBB domain (eg non-maturity deposit decay rate, beta, prepayment, etc.) Collaborate with model owners and model validation team to address ... models, ensuring appropriate design and use. Prepare high-quality, well-structured presentations of model results to senior leadership and committees. Align … more
- Merck (Rahway, NJ)
- **Job Description** **Associate Director HVAC** **:** The HVAC Associate Director is responsible for leading and developing a team that supports HVAC operations ... candidate will have strong technical expertise in HVAC design, maintenance, and validation within a highly regulated environment, combined with leadership skills to… more
- Merck (Rahway, NJ)
- …available at its Rahway, New Jersey research facility. The Principal Scientist is a senior scientific role tasked with working closely with the group Director to ... using statistical software for design of experiments. + Experience with qualification, validation , and transfer of assays to a GLP or regulated laboratory… more