- Church & Dwight Co., Inc. (Princeton, NJ)
- …record + Transitioning to Generalist in at least 1 area: Consumer products, medical device , food, dietary supplements or pharmaceutical + Contributions focused ... ensures all applicable regulations & standards across all 15 Power Brands, in Medical Devices, Drug / Homeopathics, Food / Feed / Specialty Products Division (SPD),… more
- Integra LifeSciences (Plainsboro, NJ)
- …a quantitative standpoint. The candidate must be familiar with process flow of a medical device organization, including the regulatory impact of change and ... test sequencing. + Ensure that all projects are in compliance with cGMP, cGLP, QSR (including Design Controls), ISO...in a Validation or Quality Assurance role for a medical device or pharmaceutical environment. + Demonstrates… more
- Integra LifeSciences (Plainsboro, NJ)
- …timely technical investigations and provide practical manufacturing solutions, under appropriate regulatory guidelines for Medical Device Manufacture. As ... degree or equivalent with 5+ years of experience + Experience in the medical device , pharmaceutical or similarly regulated industry with experience in process… more
- Integra LifeSciences (Princeton, NJ)
- …Regulatory , Legal, and Operations to ensure alignment across product lifecycle phases and compliance with medical device regulations (eg, FDA, ISO 13485, ... plans. + Deep knowledge of global sourcing, contract manufacturing, and regulatory compliance in medical devices. + Strong leadership, negotiation, and… more
- Bristol Myers Squibb (Princeton, NJ)
- …of industry experience in bioanalysis and/or IVD/CDx development within pharmaceutical, biotech, medical device , or CRO settings. + Direct experience managing ... CROs and external partners, managing study milestones, deliverables, and compliance with BMS quality systems and regulatory ...plans then in effect and may include the following: Medical , pharmacy, dental and vision care. Wellbeing support such… more
- ADP (Roseland, NJ)
- …audit activities. + Drive improvements in access governance and documentation. + Maintain compliance with regulatory and internal policies (SOX, GDPR, ISO 27001, ... + Align IAM and directory strategies with organizational security policies, compliance requirements, and business continuity goals. + Design and enforce Active… more
- Integra LifeSciences (Princeton, NJ)
- …Planning Modules. Strong expertise in implementation, rollouts, and enhancements for large-scale Medical Device company, ensuring compliance with industry ... & Validation** Experience ensuring GxP, FDA, and other regulatory compliance in Life Sciences supply chain...ASCP R12.2 & Cloud Demand Planning implementations and rollouts Medical Device clients, optimizing global supply chain… more
- ManpowerGroup (Wayne, NJ)
- …Engineer **Location:** Wayne, NJ **Pay Rate:** $50 per hour Our client, a leading medical device company, is seeking a **Quality Engineer II** to join their ... Engineering team. This critical role ensures the quality and compliance of medical devices throughout the product...of experience in Quality or Engineering, preferably in the medical device or pharmaceutical industry. + Experience… more
- J&J Family of Companies (Raritan, NJ)
- …labeling implementation inputs and deliverables for registration sample packs, Software as a Medical Device (SaMD), and other non-U.S. labeling in scope of GL. ... impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Regulatory Affairs Group **Job Sub** **Function:** Regulatory Product Submissions… more
- Atlantic Health System (Morristown, NJ)
- …and Compliance : Performs and oversees data collection and documentation in compliance with SOPs and GCPs. Facilitates/collaborates with regulatory staff on ... reports and documents all adverse events and serious adverse events per regulatory requirements, sponsor requirements and policies and procedures. + Writes study… more