Quality Analyst Salary at Ccc Inc BETA

The Senior Quality Control Analyst will support quality control microbiology and environmental monitoring technical support testing. The quality control microbiology programs include in-process and final drug product microbial assays such as bioburden, endotoxins, mycoplasma, gram stain, environmental monitoring, and sterility techniques. Schedule: Monday-Friday First Shift. Some weekend overtime needed. Responsibilities: Collaborate with teams to 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 GMP Quality Control laboratory testing activities with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. Support thorough GMP investigations for quality events. Author, review, and approve technical assay documents including but not limited to p

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

Job Tittle: Quality Control Analyst II Location: Fort Washington, PA, 19034 Duration: 15 Months Pay Range: $(39.00 - 40.70)/hr on W2 Job Description: Responsible for using data to determine reliability and conformance of quality control process. Accountable for identifying trends and reoccurring issues and suggesting solutions. Duties & Responsibilities: Compiles and analyses data on reoccurring product defects to determine root cause. Documents analysis results. Analyses raw material inspection logs for consistent failures. Notifies purchasing and quality departments about suppliers that have provided inferior products. Studies work processes, measurements and performance metrics to identify improvement areas. Recommends new or modified procedures based on findings. Interfaces with customers, suppliers and associates to define and improve quality standards and expectations. Participates on process improvement teams. Monitors and scrutinizes internal and external complaints and compile

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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

Shift: Wed. - Sat. 7:00am - 6:00pm Essential Functions and Responsibilities Performs deviation investigations for all areas within Quality Control Perform out of specification investigations with an emphasis on QC analytical assays (flow cytometry, ELISA, and other cell-based assays) and microbiology assays Work cross-functionally to create relevant corrective/preventative actions (CAPA). Support maintenance of a database in support of QC metrics and KPl's. Revise quality documents in support of deviation mitigation and/or CAPAs Support programs to improve on-time closure rates for all quality records. Other responsibilities as determined. Required Education, Skills, and Knowledge Bachelor's degree in a relevant discipline (biological sciences or equivalent) 1-3 years of experience in the biopharmaceutical industry within a cGMP Quality Control role Basic knowledge of biological drug development with respect to Quality Control Extremely detail-oriented with strong analytical, written,