Quality Analyst Salary at Nividous BETA

Here at Savista, we enable our clients to navigate the biggest challenges in healthcare: quality clinical care with positive patient experiences and optimal financial results. We partner with healthcare organizations to problem solve and deliver revenue cycle improvement services that enable their success, support their patients, and nurture their communities, all while living our values of Commitment, Authenticity, Respect and Excellence (CARE). Come join a leading revenue cycle management company and our growing family of cancer registry professionals! Savista is one of the largest employers of ODS professionals in the nation and we have many opportunities available across a variety of cancer registry roles. You'll work in an environment where you'll be supported by a team of strong and tenured colleagues, including our quality analysts and educators. Our focus is to help you meet your full potential and have a successful career in cancer registry, while also providing our clients wi

The Quality Analyst Sr. works with different servicing departments and internal team to ensure the business meets guidelines and perform in accordance to procedures.. The Analyst may evaluate transaction folders, correspondence between team members, consumers, clients, and third parties to ensure that the business objectives are met. This role maintains deep knowledge of the business processes, changes to existing regulations and new procedures and requirements being implemented. The position collaborates with the line of business; management team to implement successful action plans that improve overall quality metrics and ensure quality performance leading to excellent customer service. Responsibilities: Monitors changes to operational procedures from relevant Business Units and Departments Performs ongoing, structured, and rigorous testing of key procedures and controls within all business units Identifies opportunities for cost and risk reduction, efficiency gains, and enhanced lev

Job Description Job Description We are seeking a Supervisor- Workflow to join the team in our King of Prussia, PA office! The Supervisor - Workflow is responsible for overseeing the daily operations of the Workflow team, ensuring efficiency, accuracy, and compliance with company policies and industry regulations. This role involves supervising staff, optimizing workflows, and driving team performance to meet key metrics. The ideal candidate is a proactive leader with strong problem-solving skills, a collaborative mindset, and a commitment to continuous improvement. Responsibilities: Provide direction, support, and coaching to ensure the team meets departmental goals and performance standards. Oversee workload distribution, prepare daily assignments, and ensure turnaround time and service level agreements (SLAs) are met. Oversee claims setup, policy enrollments, and member eligibility verifications in accordance with company policies and regulatory guidelines. Track quality and producti

3rd Shift Quality Control, Microbiology Manager needed! Shift: Monday to Friday from 11:00pm to 7:30am Essential Functions and Responsibilities: Manage several analysts in the day-to-day cGMP QC testing of drug products for lot release and stability; Manage microbial testing at contract laboratories Manage the technical transfer, qualification, and validation of microbiology test methods for in- process materials, lot release, and/or stability, as needed Manage the environmental monitoring program for the facility Author, review, and approve SOPs, protocols, reports, specifications, and other quality control documents. Ensure trend analysis and trend reports for environmental monitoring data are performed timely. Lead investigations for out-of-specification test results, corrective actions, and verification of effectiveness. Support product stability programs including generation of stability protocols, execution of stability testing, stability data analysis, and final reporting of sta

Sr. QC Analyst, Microbiology needed! Overview: The Senior Quality Control Analyst- Microbiology will support quality control testing operations. The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxins, mycoplasma, gram stain, environmental monitoring, and sterility techniques. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to complete assigned work. Essential Functions and Responsibilities: Perform daily cGMP quality control laboratory microbiological testing activities. Perform environmental monitoring of the cleanroom areas as scheduled. Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times. Perform all activities for cGMP compliance. Support thorough cGMP investigations for out-of-specification test results. Support technical problem-solving. Su

Quality Control Supervisor needed! Overview: Seeking a Quality Control (QC) Supervisor in Raw Materials, who will be responsible for oversight and management of the QC Raw Material Program. The manager will be expected to manage and oversee the responsibilities relating to the sampling, release testing, data review, and vendor qualification, for all raw material lots received for use in the manufacturing of product. These activities include chemical and biological raw materials, component inspection, and final packaging. A good understanding of QC test methods and raw materials release requirements per USP and EP compendia, is desired. Experience working in a GMP-regulated environment is essential. The position will report to the Senior Manager, Quality Control – Raw Materials. Shifts available: Mon-Fri, 8am-5pm & Mon-Fri, 2pm-11pm (shift differential included) Essential Functions and Responsibilities: Schedule and manage the day-to-day raw material release operations, including Accept

Senior Quality Control Analyst needed! Overview: Seeking a Senior Analyst, Quality Control (QC) Raw Materials, who will be responsible for the sampling, release testing, data review, and vendor qualification, for all raw material lots received for use in the manufacturing of product. These activities include chemical and biological raw materials, component inspection, and final packaging. A good understanding of QC test methods and raw materials release requirements per USP and EP compendia, is desired. Experience working in a GMP-regulated environment is essential. The position will report to the Raw Materials - QC Manager, 3rd Floor Laboratory. Essential Functions and Responsibilities: Support the planning and establishment of the initial setup of internal raw material testing laboratory. Perform day-to-day activities for raw material release testing, including but not limited to USP<71> Sterility, USP <61> Growth Promotion, USP <63> / EP 2.6.7 Mycoplasma, USP<85> Bacterial Endotoxin

Duties: Perform assay co-qualification, validation, and technical transfer of updated and new assays, as well as potential new products. Act as subject matter expert (SME) and train new laboratory personnel on assays. Perform all activities with respect to GMP/GDP compliance. Qualifications: Bachelor’s degree in Biology, Biochemistry, Microbiology, Chemistry, or related scientific field or equivalent combination of education and experience. Minimum three (3) years of GMP experience in the pharmaceutical industry within a Quality Control Solid understanding and functional knowledge with hands-on experience with two (2) or more of the following: endotoxin, mycoplasma, bioburden, sterility. Experience in technical writing (e.g., technical reports, test methods, SOPs, protocols, deviations, CAPAs, change controls, etc.) Pay Scale: $115,000 – $125,000 (Dependent on Experience) R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, cl