- Sanofi Group (Morristown, NJ)
- …Regulatory Affairs (GRA), Regional GRA, Country Regulatory Groups, Technical and Quality Groups within R&D and Industrial Affairs, Regulatory Health Authorities, and ... (Global Regulatory Affairs Team) + Assures effective involvement with change control systems. + Interpret global regulations & appropriately apply, implement, and… more
- Integra LifeSciences (Plainsboro, NJ)
- …processing is performed in compliance with Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP's) and Health and ... requirements. Operate in a team environment focused on daily milestones and quality throughput. **ESSENTIAL DUTIES AND RESPONSIBILITIES** **-** to perform this job… more
- Integra LifeSciences (Plainsboro, NJ)
- …processing is performed in compliance with Good Manufacturing Practices (GMP), Quality Systems Regulations), Standard Operating Procedures (SOP's) and Health and ... in a team environment focused on daily milestones and quality throughout.This is a 1st Shift, 7:00 am to...(SOP's), and Health and Safety requirements. * Interface with QA/ QC /Material departments during course of work to coordinate inspections… more
- Bristol Myers Squibb (Summit, NJ)
- …to achieve the desired reliability. + Communicates with other departments (Manufacturing, QC , and Warehouse) to develop and meet reliability requirements to ensure ... + Develops and follows strict Standard Operating Procedures (SOP's) to ensure quality , and that compliant maintenance activities are completed in a timely manner.… more
- Integra LifeSciences (Plainsboro, NJ)
- …processing is performed in compliance with Good Manufacturing Practices (GMP), Quality Systems Regulations), Standard Operating Procedures (SOP's) and Health and ... Operate in a team environment focused on daily milestones and quality throughout. **Essential Duties and Responsibilities** + Operate, maintain, and troubleshoot… more
- Integra LifeSciences (Plainsboro, NJ)
- …processing is performed in compliance with Good Manufacturing Practices (GMP), Quality Systems Regulations), Standard Operating Procedures (SOP's) and Health and ... Operate in a team environment focused on daily milestones and quality throughout. **Essential Duties and Responsibilities** + Operate, maintain, and troubleshoot… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …Programmer can include:** * Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data ... documents). * Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval,… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- JOB RESPONSIBILITIES: * Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models ... documents). * Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval,… more
- Integra LifeSciences (Plainsboro, NJ)
- …to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP's), and Health and ... support teams to ensure continuous production of the correct product at high quality levels with minimal wasted time and materials + Responsible for performing… more
- Cytel (Trenton, NJ)
- …and deliverables are aligned with the relevant regulatory requirements. Responsible for quality control and audit readiness of all assigned statistical ... of experience in biostatistics or statistical programming activities in the Pharmaceutical or Biotechnology industry in clinical development, including: 2 years of… more