- Merck & Co. (Rahway, NJ)
- …site contact and site manager throughout all phases of a clinical research study,-taking overall responsibility of allocated sites.Actively develops and expands ... the territory for clinical research, finding and developing new-sites. Participates in internal meetings and workstreams as SME for monitoring processes… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Senior Specialist, Process Engineer The Small Scale Organics (SSO) Pilot Plant is a Good Manufacturing Practices (GMP) facility ... enables gain of critical internal experience during scale-up of clinical supplies manufacturing, demonstration of new manufacturing technology/processes, training… more
- Merck & Co. (Rahway, NJ)
- …approval of documentation to support Good Manufacturing Practice (GMP) - clinical supply API manufacture, testing, release, and maintenance in support of our ... Job DescriptionThe Rahway based Senior Specialist, Global Development Quality Operations - API,...improvement and efficiency. Support the implementation of the clinical supply QMS through participation as topic team member… more
- Merck & Co. (Rahway, NJ)
- …provides a high degree of technical and project management responsibility. The Senior Specialist - Process/Facility Engineering position will report to the Director, ... development of new technologies/capabilities, execution of capital and non-capital improvement projects, and interfacing with the automation system assets spanning… more
- Catalent (St. Petersburg, FL)
- …support over the lifecycle of all products, driving continuous improvement throughout the manufacturing environment facilitating commercial technology transfers and ... during the new product introduction process.The primary tasks performed by the Senior Lead Investigator will include working on proper investigation and … more
- Merck & Co. (Rahway, NJ)
- …provides a high degree of technical and project management responsibility. The Senior Specialist - Manufacturing Automation position will report to the Director, ... development of new technologies/capabilities, execution of capital and non-capital improvement projects, and the automation system assets spanning production,… more
- Catalent (San Diego, CA)
- …Diego, CA is hiring a Senior Manager of Quality Assurance (QA) at our Clinical Supplies facility. As a member of the Site Leadership Team, you will partner with ... Senior Manager, Quality AssurancePosition Summary:Catalent Pharma in San...site culture of Safety, Quality performance, Operational Excellence, continuous improvement , error reduction, regulatory compliance, and sound fiscal responsibility.… more
- Catalent (Harman, WV)
- …materials release, and compiling, trending and reporting key quality metrics for Senior Management review, and other quality system functions, as needed. The Role ... staff are fully trained on all cGMP manufacturing operations and documentation and adhering to safety guidelines Build effective teams that apply… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Business Units. Provide strategic and proactive QA Leadership for respective GPTs and Clinical Programs in close alignment with the Head of R&D QA. Within assigned ... the review of Key Quality Indicators (KQIs). Identify appropriate continuous improvement initiatives for quality and compliance related areas. Deputize for the… more
- Merck & Co. (Rahway, NJ)
- …management responsibility. -The Director - Automation Leader position will report to the Senior Director, Enabling Facilities, and will be a member of the EF ... development of new technologies/capabilities, execution of capital and non-capital improvement projects, and the automation system assets spanning production,… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …employees. Responsible for the reviews of direct reports with the input from senior management. May provide general or direct supervision to exempt employees and/or ... trends Oversees the scheduling of laboratory work in support of commercial, clinical and/or pre- clinical programs as needed Supervises laboratory activities in… more
- Elite Staffing Inc. (Louisville, KY)
- Senior Health Information Scientist As a Senior Health Information Scientist at Ontada, you will design information systems that power analytics and data ... * Organize data across contexts to identify opportunities for improvement . * Own the conceptual and logical model for...forms of data. * Lead the marriage of operational, clinical , laboratory and other data structures. * Advocate for… more
- Compass Health Network (St. Peters, MO)
- …and behavioral health, prevention, and wellness through quality assurance and improvement * Develop and maintain policies, procedures, and processes related to the ... nursing and physician consultant services* Work collaboratively with administrative and clinical leadership to ensure that DD HH activities are integrated into other… more
- Exact Sciences (Phoenix, AZ)
- …workflows and develop new automated workflows in a complex, rapidly evolving clinical laboratory. The Senior Engineer responsibilities may include assisting Lab ... life while you're working to help others. Position Overview The Senior Engineer, Process Development and Automation coordinates, manages, implements, and provides… more
- Behavorial Health Network, Inc (Springfield, MA)
- …seeking a dedicated Quality Supervisor to elevate our standards and drive continuous improvement . If you have a passion for maintaining high-quality Processes Join a ... Supervisor is responsible to providing successful quality assurance and quality improvement processes of the care management program, serving adults with chronic… more
- Integrated Resources, Inc (Sanford, NC)
- …. You will evaluate and review manufacturing related activities in support of clinical and commercial batch production. . Your expertise will help in identifying ... deviations from established standards, in the manufacturing of clinical and commercial batches. . In the relevant cases you will approve change control activities to… more
- Geisinger (Danville, PA)
- Job Summary The Clinical Documentation Improvement Program (CDI) is designed to improve the physician's documentation in the patient's medical record, ... of care of the patient. The role of the Clinical Documentation Improvement Specialist (CDIS)...dental and domestic partners. Perhaps just as important, from senior management on down, we encourage an atmosphere of… more
- HCA Healthcare (Nashville, TN)
- …work environment where diversity and inclusion thrive? Submit your application for our Clinical Documentation Improvement Liaison opening with Parallon today ... benefits may vary by location._** We are seeking a Clinical Documentation Improvement Liaison for...a healthier tomorrow."- Jane Englebright, PhD, RN CENP, FAAN Senior Vice President and Chief Nursing Executive If you… more
- Ascension Health (Saginaw, MI)
- …+ Maintain accurate records of review activities, ensuring reports and outcomes of clinical documentation improvement (CDI) efforts are valid. + Provide ... Clinical Documentation Professional credentialed from the Association of Clinical Documentation Improvement Specialists (ACDIS)Coding credential and… more
- Corewell Health (Grand Rapids, MI)
- …regulations, organizational policy and accreditation/compliance requirements. + Prepares detailed clinical summaries and/or other clinical documentation ... in current data and healthcare trends as it relates to appropriate clinical documentation and evidenced-based medicine. + Utilizing project management skills,… more