- Merck & Co. (Rahway, NJ)
- …organizations ( as a lead GCS Planning program representative ) such as clinical development, regulatory, quality and other supply chain areas to negotiate ... cost estimates requested by Product Development Teams . - Responsible for authoring clinical supply documentation in support of labeling and packaging activities… 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 ... Drug Product and Clinical Finished Goods).- - Responsible for authoring clinical supply documentation in support of labeling and packaging activities as… 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 ... quality systems records.Support CAPA site governance programDrive continuous improvement of quality systems processes.Ensure compliance with current Good… more
- Merck & Co. (Rahway, NJ)
- …Design, Process Hazard Analysis (PHA), Process Optimization, Project Management System, Quality Management, Quality Management System Improvement , ... Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply (PSCS)The FLEx sterile facility supports the formulation and filling… more
- Merck & Co. (Rahway, NJ)
- …executing batch production work. Additional responsibilities include coordination, planning, documentation , and other facility improvement activities. Position ... aiding technology development, and supplying Active Pharmaceutical Ingredient (API) for clinical use and drug product development. This will involve handling of… more
- Eisai, Inc (Raleigh, NC)
- … management system.Conduct ongoing tracking, documentation , and reporting of quality goals and metrics.Participate in process improvement activities aimed to ... to hear from you. The QA Specialist plays a critical role in ensuring the quality and compliance of commercial and clinical products manufactured at the Eisai… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …This role will work with Global Regulatory Affairs and cross-functional teams (eg, Quality , CSPV, Clinical Operations, Clinical Development, RA CMC) to ... function, responsible for ensuring Daiichi Sankyo's Regulatory processes & procedural documentation are fit for purpose and compliant with relevant regulations.… more
- Aequor (Thousand Oaks, CA)
- …GMP standards are maintained in line with current SOPs, batch record documentation , and licenses. Identifying improvement opportunities within the organization ... vital to the impact that ATO B20 with a clinical and commercial product mix has to the network....value to the network: Manufacturing, Process Development, Supply Chain, Quality , and Facilities & Engineering. A high degree of… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …be responsible for maintenance support and mechanical system operations for cGMP Clinical and Commercial Cell Therapy Manufacturing on a modified second shift ... requirements. This individual will support the organization in its build and ramp-up of clinical production and facility approval of a state of the art cell therapy… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …management experience required. Comfort operating in a fast-paced, environment, with a quality control focus and a documentation orientation Innate intellectual ... methodologies to provide key insights into the biopharmaceutical landscape across clinical , commercial, and enterprise domains. This role involves applying data… more
- Merck & Co. (Durham, NC)
- …the Master Data team with general Material Handling Steward tasksDrive safety, quality and process enhancements throughout the supply chain - Project Management Lead ... project to upgrade overall discard process Primary Responsibilities, Continuous Improvement and Stakeholder Collaboration Lead cross-functional teams to execute… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …with strategic alignment Effective in fast-paced environments with a focus on quality and documentation Skilled in change management and guiding teams ... cutting-edge AI/GenAI technologies and developing AI/GenAI products to deliver high quality insights with speed and efficiency Promotes a culture of creativity… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …with strategic alignment.Effective in fast-paced environments with a focus on quality and documentation .Skilled in change management and guiding teams ... Operations, including but not limited to - Commercial, Patient Services, CMR ( Clinical , Medical, Regulatory), Finance, and Novo Nordisk global colleagues, to deliver… more
- Elevance Health (Seattle, WA)
- …a minimum of 10 years of experience in claims auditing, quality assurance, or clinical documentation improvement , and a minimum of 5 years of experience ... with third party DRG Coding and/or Clinical Validation Audits or hospital clinical documentation improvement experience preferred. + Broad knowledge of … more
- Dignity Health (Redding, CA)
- …least 5 years experience in quality improvement and/or inpatient clinical documentation improvement , with knowledge of ICD-10 and chart abstraction ... coding regulations and guidelines. Independently uses knowledge of clinical medicine, clinical documentation , and quality reporting rules and procedures… more
- Rochester Regional Health (Rochester, NY)
- …case-mix and quality measures. The Director provides daily oversight of Clinical Documentation Improvement Team across multiple facilities and is ... Riedman CampusHours Per Week: 40Schedule: Monday - Friday, 8am - 4:30pmSUMMARY The Clinical Documentation Improvement Director provides a key role in… more
- Mount Sinai Health System (New York, NY)
- …cases in 3M. Reviews and reconciles DRG discrepancies between DRGS/APR's and the Clinical Documentation Quality Improvement (CDQI) department. Develops ... secondary review is required to verify assignment of Patient Safety Indicators, HAC, Clinical Documentation Improvement ,Sepsis and any other charts meeting… more
- AdventHealth (Altamonte Springs, FL)
- …integrity, and ability to function as a liaison to the Quality and Clinical Documentation Improvement teams for the Multi-State Division. Assigns codes ... work with Case Management, the Billing Office, Coding Manager, Clinical Documentation Improvement specialists and...documentation . Will work in conjunction with CDI, HIM, Quality , and Informatics leadership across the division to create… more
- Athena Health Care Systems (Providence, RI)
- …+ Promote a systematic approach to quality assurance, resident satisfaction, and clinical documentation improvement . + Serve as a liaison and consultant ... management program. In conjunction with other operational director, revise the clinical quality improvement program, as necessary. + Coordinate with … more
- Veterans Affairs, Veterans Health Administration (Fayetteville, NC)
- …health status of patients. Develops and/or updates medical center policy pertaining to clinical documentation improvement . Serves as a technical expert in ... documentation requirements. Responsible for reviewing the overall quality and completeness of clinical documentation...degree or higher, and three years of experience in clinical documentation improvement (candidates must… more
