- Merck & Co. (Rahway, NJ)
- …#VETJOBS Required Skills: Adaptability, Adaptability, Change Control Processes, Change Management, Clinical Development, Clinical Documentation , Clinical ... supplies. Interacts with key partner organizations such as clinical development, regulatory, quality and other supply...and Clinical Finished Goods). Responsible for authoring clinical supply documentation in support of labeling… more
- Merck & Co. (Rahway, NJ)
- …Development Quality Operations, is responsible for independent approval of documentation to support GMP clinical supply drug product manufacture, testing, ... 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)
- …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, Laboratory & ... Experimentation) center, with a primary focus on sterile clinical manufacturing within Pharmaceutical Sciences (Pharm Sci), Pharmaceutical Operations Engineering… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The** **Position** The Clinical Trial Manager (CTM), Translational Medicine and Early Development (TMED) is responsible for assisting in the ... of contact for study vendors. The CTM will also assist to manage the clinical study team and help to coordinate meetings and interactions with vendors to optimize… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking an Operations Specialist as part of the Technical Operations team based in Raritan, NJ.Role ... position will be responsible for providing operational support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will partner… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality , or cell ... of multiple myeloma.Legend Biotech is seeking a QA Validation Specialist III as part of the Quality ...within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the candidate has experience working in a cGMP manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality , or cell ... multiple myeloma.Legend Biotech is seeking a QA Change Control Specialist II as part of the Quality ...within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …have relevant working experience in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality , technical ... multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist III as part of the Quality ...provide guidance and determine immediate path forward for manufacturing quality issues.Review of all documentation , in accordance… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Operations Support Specialist as part of the Technical Operations team based in Raritan, NJ. ... Role OverviewThe Operations Support Specialist will be part of the Technical Operations team...production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking CQV Specialist II as part of the Technical Operations team based in Raritan, NJ. ... for providing Commissioning, Qualification and Validation support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will be… more
- ALWAYS COMPASSIONATE HEALTH (Melville, NY)
- …and innovation to enhance each patient's quality of life. TItle: Clinical Documentation Specialist / Quality Assurance LPN Location: Melville, ... Licensed Home Care Service Agency which provides the highest quality of community home-based services, combined with exceptional compassion...Nurse (LPN) to join our Melville team as a Clinical Documentation Specialist . This individual… more
- Deloitte (New York, NY)
- …physician, physician assistant, case manager, clinical documentation specialist , utilization review, informatics RN, Quality , DRG Validation and health ... Healthcare Clinical Documentation Specialist -...skills to collaborate with clinicians, physicians, NP/PAs, ancillary departments, Quality , Case Management, Finance, Revenue Cycle, and Coders +… more
- Hackensack Meridian Health (Neptune City, NJ)
- …as a leader of positive change. The ** Clinical Documentation Specialist RN** facilitates improvement in the overall quality , completeness and accuracy of ... Certifications Required:** + Current state Registered Nurse license. + Certified Clinical Documentation Specialist (CCDS) or certification within two (2)… more
- Northwell Health (Lake Success, NY)
- …lab management. Reviews and evaluates lab processes and recommends quality and/or process changes. Job Responsibility Investigates complaints, implement solutions ... to establish and collect performance improvement metrics Collects, prepares and analyzes quality reports for trends. Work with lab management for action plans as… more
- Medtronic (Manhattan, NY)
- …region. A valid driver's license is essential for this role. At Medtronic, the Clinical Specialist , supports the Neuromodulation Pain and Target Drug Delivery as ... weekends and after hours and at the discretion of Clinical Specialist Manager + Adheres to company...company policies and complies with required event reporting and documentation , utilizing Medtronic technology tools + Responsible for managing… more
- Cook Medical (New York, NY)
- Overview The Clinical Specialist provides clinical support for extensive medical device product lines through direct physician interaction, medical staff ... information about Cook Medical, visit www.cookmedical.com Responsibilities * Provide clinical support during procedures* Identify, establish, support and develop… more
- MVP Health Care (Tarrytown, NY)
- …agencies. + Work closely with internal and external stakeholders to support clinical documentation , ensuring accuracy and compliance with organizational and ... and continuous improvement. To achieve this, we're looking for an **Associate, Post-Acute Clinical Support Specialist ** to join #TeamMVP. If you have a passion… more
- Merck (Rahway, NJ)
- …**Required Skills:** Adaptability, Adaptability, Change Control Processes, Change Management, Clinical Development, Clinical Documentation , Clinical ... supplies. + Interacts with key partner organizations such as clinical development, regulatory, quality and other supply... Clinical Finished Goods). + Responsible for authoring clinical supply documentation in support of labeling… 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
