- Fujifilm (Wayne, NJ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... **Position Overview** This position is responsible for technical repair and final quality inspection on assigned Endoscopic units. This position is responsible for… more
- Catalent Pharma Solutions (Bridgewater, NJ)
- …understanding of financial and business concepts. + Experience working to regulatory standards: FDA , Good Engineering Practice (GEP), Good Manufacturing ... of commercial and late-stage clinical products efficiently, timely, and with high quality . Scope of the role covers the entire product lifecycle including M&A,… more
- Bristol Myers Squibb (Summit, NJ)
- …the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed ... production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. Day shift structures are… more
- RWJBarnabas Health (Long Branch, NJ)
- …routine and advanced mammography procedures within the scope defined by regulatory and departmental standards. Qualifications: Required: + ARRT Certification in ... in maintaining current continuing education credits as required by the FDA /MQSA and ACR Preferred: + Previous Mammography experience Scheduling Requirements: +… more
- Bristol Myers Squibb (Summit, NJ)
- …the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed ... production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. Start and end times are… more
- Bristol Myers Squibb (Summit, NJ)
- …the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed ... production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. **Shift Available:** + Quad… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …a structured design and development process is followed, ensuring compliance with quality management systems and regulatory requirements, where applicable. + ... complex projects delivering the right outcomes balancing on time delivery, budget, quality and market and customer expectations. Highly skilled in integrated program… more
- BioLife Plasma Services (Trenton, NJ)
- …and build your skills by contributing to financial, marketing, administrative, regulatory , quality , people, and facilities management. + **Contribute to ... Creating Life-Changing Medicines:** Maintaining our exceptional quality and service standards is key to creating life-changing...Experience working with SOPs, GDP, GMP, CLIA, and the FDA + Experience working in a highly regulated environment… more
- Integra LifeSciences (Plainsboro, NJ)
- …must be familiar with process flow of a medical device organization, including the regulatory impact of change and the documentation path of a compliant process. The ... + Change control, non-conformance and CAPA support. + Participate in FDA inspections, ISO certifications, surveillance audits and customer audits. **QUALIFICATIONS**… more
- Fujifilm (Trenton, NJ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and procedures. + Effective communication within FUJIFILM IVD organization of sales, quality and compliance issues. + Utilization of the IVD reporting systems for… more