Director, Quality Assurance Salary at Cades BETA

About Taylor Fresh Foods, Inc. Taylor Fresh Foods, Inc. is dedicated to being North America’s favorite maker of salads and healthy fresh foods. Our “Taylor Family” includes over 24,000 team members who are passionate about making high quality, great tasting products for families across North America. As we continue to rapidly grow, we have a career opportunity available for a talented and motivated individual to join our Taylor Farms New Jersey team as Retail Production Manager location in Swedesboro, New Jersey. JOB SUMMARY: Reporting into the Director of Operations, the Production Manager is responsible for both the quality and cost of all production at the NJ Retail facility. The Production Manager is expected to surpass budget regarding cost of product, labor goals, efficiency standards, as well as expectations for quality throughout production runs. Having ultimate control over all direct labor in the plant, the Production Manager oversees via direct reports, approximately twenty-

Job Type Full-time Description EwingCole is a nationally recognized architecture, engineering, interior design and planning firm with offices across the country. Our multi-disciplinary practice is built on the core values of professional excellence, design quality and collaboration. We are seeking a Quality Assurance Architect (QAA) to join our Philadelphia office. The QAA assists the QA Department in overall Quality Assurance/Quality Control at EwingCole. The QAA supports the Firm's efforts for project specific solutions, working with teams of architects, engineers, consultants, and other team members and plays a critical role in achieving the firm's goals of quality design and exemplary service. Member of the QA Department, a group of dedicated, technically focused professionals. Quality review production drawings and specifications for a variety of projects and project-related data to verify design compliance with project, client, and industry standards, including constructability a

Manager, Clinical Quality Assurance This position is responsible for overseeing GCP/Clinical Quality Assurance activities with an industry leader in NASH/MASH Therapies. The main objective is to ensure the quality and compliance of clinical trials sponsored by a leading biopharmaceutical company focused on innovative therapeutics. This includes adherence to relevant GCP regulations, ICH GCP guidelines, company SOPs, and current industry standards and best practices. You will be partnering with the Sr. Director of Quality on this fully remote position. Position Responsibilities: Establish and maintain clinical quality systems and processes to ensure adherence to GCP, FDA, EMA, and other global regulatory requirements, fostering a culture of quality from the initiation of clinical trials to ensure patient safety and data integrity. Collaborate across functions to apply a risk-based approach to compliance and participate in regular internal and external study team calls for ongoing qualit

Job Description Job Description Description: Salary: $40,000 Job Status: Full-time and on-site Location: 4301 Rising Sun Avenue, Philadelphia, PA 19140 ABOUT APM Asociación Puertorriqueños en Marcha (APM) has been helping families achieve their greatest potential since 1970 by providing early childhood education, foster care & adoption, child welfare, mental & behavioral health, community and economic development, housing, community school services, and violence intervention services to the North Philadelphia communities. SUMMARY The Quality Assurance is responsible for ensuring that the Behavioral Health is adhering to established performance and quality standards. Specifics duties include tracking performance data and generating reports, reconciling program data, and performing other tasks as assigned. Some of the duties and responsibilities are: Overall Responsibilities Assist in the process of updating department policies and procedures. Provide feedback and collaborate with admini

Grade: T28 The link below will give you information about the University's T scale. careers.temple.edu/sites/careers/files/documents/T_Salary_Structure.pdf A variety of important factors are reviewed by HR when considering salary, including job duties, the applicant's education and experience, all relevant internal equity considerations, department budget, and funding source. Reporting to the Assistant Dean and Medical Director in the School of Podiatric Medicine (TUSPM), the Director of Operations- Compliance, Quality Assurance and Surgery Center directs and oversees all administrative and technical elements of the Ambulatory Surgery (ASC-currently inactive), including the function of Director of Nursing. In addition, this position directs the Quality Assurance (QA), compliance and Utilization Review (UR) functions for all TUSPM health services divisions and the entirety of TUSPM as appropriate, including the ASC, Foot and Ankle Institute (FAI) and its satellite and physical therapy p

Job Description Job Description Quality Assurance Specialist for Command Level I Program NSWCPD Code 00Q Philadelphia, PA Responsibilities: Position is for the Quality Assurance Specialist, NSWCPD Code 00Q support, to be part of team supporting Quality Assurance and Technical Administration Support services. This support will include supporting: Quality Management System Program, Systems Engineering Process (SEP) Quality Assurance Program, Shipboard Work Quality Assurance Program, Command Level I Material Program, SUBSAFE Program Office, Special Programs/Test Site Quality Assurance, and Naval Foundry Propeller Center (NFPC). The primary support will be to the NSWCPD Quality Management Office C/00Q Quality Management System (QMS). The QMS is focused on consistently meeting customer requirements and enhancing customer satisfaction, ensuring that functional areas are compliant with Navy standards and the NSWCPD QMS. The QMS Division ensures that the performance and quality of services con

STA is constructing new facilities to manufacture small molecule drug products. This will include capabilities for oral solid as well as sterile dosage forms manufacturing. As well as the supporting analytical, warehousing and other needed capabilities. The position will initially lead the team (including consultancy firms) responsible for the quality and compliance support during design, construction and qualification phases of these facilities. And will be responsible for the implementation of the quality system. After start of operations and manufacturing, this position will take overall quality leadership responsibility, managing the QA team supporting the Quality system, Product release and continuous quality. The individual will keep close cooperation with the Site Leadership Team, and will develop the Quality assurance team to support the creation of a culture that aligns with the Company’s core values of integrity & dedication, working together, doing the right thing, and doing

ESSENTIAL FUNCTIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of knowledge, skill, and/or ability required. Ensure that all HPSI safety procedures, rules and regulations are followed and met. Administer the team timekeeping process. Assign tasks to, monitor and coach the QC Coordinators and Inspectors. Quality Director as applicable when they are absent. Ensure that all QC Inspectors and Coordinators have the proper equipment required for the execution of their duties. Provide training and coaching to all subordinates in all QC procedures, methodology and processes. Record all training on a record of training. Resolve conflicts that may arise between QC and production personnel. Fully conversant with ISO 9001:2015 certification and internal quality system audits. Evaluate the performance of direct reports. Perform other related duties as required and assigned. Review and f