- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... find better and more innovative ways to improve their quality of life. We're changing lives for a living....you ready to make a difference? The Position The Specialist , Regulatory Operations - Submissions supports the development of… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... find better and more innovative ways to improve their quality of life. We're changing lives for a living....performance and growth. Relationship This job reports to the Senior Director of the GxP Compliance & Technical Operations… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Rahway based Senior Specialist , Global Development Quality Operations, is responsible for independent approval of documentation to support ... Quality representative for in-house or outsourced manufacturing for clinical supplies.- Duties include compliance oversite of program-related activities, batch… more
- Merck & Co. (Rahway, NJ)
- …for clinical supplies. Interacts with key partner organizations such as clinical development, regulatory, quality and other supply chain areas to address ... and prepares, analyses, and/or develops mitigation strategies for review with clinical partners and senior leaders. Works directly in the SAP system to establish… more
- Merck & Co. (Rahway, NJ)
- … Clinical Trial Operations (GCTO) Regional colleagues and Global - Development Quality (GDQ) to address clinical supply related topics. - Responsible and ... deliverables and prepares, analyzes, and/or develops mitigation strategies for review with clinical partners and senior leaders. - Responsible and accountable… more
- Merck & Co. (Rahway, NJ)
- …with the communications roadmap. Partner with development teams to ensure high- quality delivery using Agile methodologies. Act as product owner through delivery, ... communications comply with relevant regulations and standards, partnering with compliance and quality teams as needed. Risk & Issue Management Capture and manage… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Automation Specialist provides end-to-end automation and quality engineering support for the Rahway, NJ FLEx (Formulation, ... & Experimentation) center, with a primary focus on sterile clinical manufacturing within Pharmaceutical Sciences (Pharm Sci), Pharmaceutical Operations Engineering… more
- Merck & Co. (Rahway, NJ)
- …from the Director/Associate Director Publication Management, the Sr. Specialist Publication Manager coordinates publication planning and implementation, tracks ... and Lexicon for the products they support. The Sr. Specialist Publication Manager serves as the point to the...of interest or strong scientific background Understanding of the clinical development process, clinical study data and… more
- Merck (Trenton, NJ)
- …and saving lives around the world. Our Research & Development Division QA Clinical Quality (CQ) provide independent assurance that our Company ensures the ... to the Auditor Resourcer include:** + Support, advance, and drive the Clinical Quality capacity planning and assignment of GCP audits + Lead our Research… more
- Medtronic (Manhattan, NY)
- …expectations by striving without reserve for the greatest possible reliability and quality in our products, processes and systems by being accountable, having a ... Medtronic Careers (https://medtronic.wd1.myworkdayjobs.com/MedtronicCareers) **Primary Responsibilities** + Provide technical, educational, clinical and sales support to assist the Region in… more
- Merck (Rahway, NJ)
- **Job Description** The Rahway based ** Senior Specialist , Global Development Quality Operations** , is responsible for independent approval of documentation ... Quality representative for in-house or outsourced manufacturing for clinical supplies. Duties include compliance oversite of program-related activities, batch… more
- Deloitte (Morristown, NJ)
- Healthcare Clinical Documentation Specialist - Senior Consultant Our Deloitte Regulatory, Risk & Forensic team helps client leaders translate multifaceted ... nurse, physician, physician assistant, case manager, clinical documentation specialist , utilization review, informatics RN, Quality , DRG Validation and… more
- Bristol Myers Squibb (Warren, NJ)
- …than here at BMS with our Cell Therapy team. **Position Summary** The Senior Specialist supports the successful operation of facilities, laboratories, and ... according to established policies and procedures. **Role & Responsibilities:** The Senior Specialist supports the Commissioning, Qualification, and Validation… more
- Merck (Rahway, NJ)
- **Job Description** The Senior Automation Specialist provides end-to-end automation and quality engineering support for the Rahway, NJ FLEx (Formulation, ... & Experimentation) center, with a primary focus on sterile clinical manufacturing within Pharmaceutical Sciences (Pharm Sci), Pharmaceutical Operations Engineering… more
- Merck (Rahway, NJ)
- …from the Director/Associate Director Publication Management, the Sr. Specialist Publication Manager coordinates publication planning and implementation, tracks ... and Lexicon for the products they support. The Sr. Specialist Publication Manager serves as the point to the...interest or strong scientific background + Understanding of the clinical development process, clinical study data and… more
- Deloitte (Morristown, NJ)
- Senior Data Scientist, Specialist Senior - SFL Scientific Our Deloitte Strategy & Transactions team helps guide clients through their most critical moments ... in building industry-specific, artificial intelligence (AI) technologies. We are hiring a Senior Data Scientist to collaborate directly with clients to design and… more
- Bausch + Lomb (Trenton, NJ)
- …regulatory strategies for development programs and marketed products across CMC and clinical /non- clinical , labeling, adpromo areas. Serve as a strategic advisor ... + Formulate, lead, and drive integrated regulatory strategies across CMC and clinical /non- clinical , labeling, adpromo domains. + Provide technical expertise and… more
- Bristol Myers Squibb (Somerset, NJ)
- …innovative bio-pharma companies, and make a difference. **Position Summary** The Therapeutic Area Specialist (TAS) is a critical role in our unique customer model to ... BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in...software or CRM tools to collect, enter, and manage quality data in a timely and compliant manner, track… more
- Merck (Rahway, NJ)
- …for clinical supplies. + Interacts with key partner organizations such as clinical development, regulatory, quality and other supply chain areas to address ... and prepares, analyses, and/or develops mitigation strategies for review with clinical partners and senior leaders. + Works directly in the SAP system to… more
- Merck (Rahway, NJ)
- … Clinical Trial Operations (GCTO) Regional colleagues and Global - Development Quality (GDQ) to address clinical supply related topics. - Responsible and ... deliverables and prepares, analyzes, and/or develops mitigation strategies for review with clinical partners and senior leaders. - Responsible and accountable… more
