Quality Assurance Associate Salary at Dr Knoell Consult Gmbh BETA

Overview: This position is responsible to plan, organize, direct, and lead the personnel and work process of the quality management program. 18 years of age A bachelors degree from an accredited college or university in social work, psychology, health sciences, business, healthcare administration, health information management or a related field. Master's degree is preferred. Three years of work experience with youth and/or adolescents in the healthcare field. Possess knowledge of the CQI (continuous quality improvement) process and the ability to apply concepts to varied activities. Excellent training, presentation and leadership skills. Responsibilities: Knowledge, Skills and Abilities: ? Possess and maintain a valid drivers license. ? Ability to pass a Criminal Record History Clearance and a Child Abuse History Clearance. ? Ability to physically participate in the use of therapeutic holds and to be certified biannually to demonstrate competence. ? Ability to participate in trauma in

Description Title: Quality Assurance Associate Job Purpose: To mainly provide support to the CAPA System, Trainings and Vendor qualification process and records review. Main Duties and Responsibilities: Maintain the culture of the importance of an integrated quality system within the company Trainer of topics related to Quality for vendors and MKN employees Support in THE CAPA System Completion of investigations via effective investigation of deviations and the development of effective action plans Completion of CAPAs and Effectiveness Checks Preparing deviation reports Support the Vendors Qualification process Assist with the "Document Control" process Maintain quality policies and procedures in accordance with company requirements Evaluate and approve documents according to the organization's standards and local regulations Instructions / SOP creation and review Collaborate with the logistics team to monitor the entire process, ensuring the effectiveness and compliance of all operati

Description Quality Assurance Associate I, PHL Main Duties and Responsibilities 1. Implement, communicate and maintain company's quality systems at the facility, in compliance with Marken's Global Quality Management System (QMS) requirements. 2. Interact with clients on Quality Assurance (QA)/ GxP related matters under management supervision. 3. Effectively interact with Marken Departments and stakeholders to maintain that all QA tasks are appropriately supported by QA. 4. Support on internal audits including report preparation and assessment and tracking of associated corrective and preventive actions (CAPA). 5. Support audits of external service providers as part of the vendor selection process. Follow up and tracking all commitments for actions or changes made by Marken from previous audits, including report preparation. 6. Support client audits and regulatory inspections, including the preparation of appropriate materials required within those audits when applicable. 7. Collate iss

About the Role: Gore Fabrics is looking for a Supplier Quality Assurance Associate to join our Quality Assurance team. In this role, you will participate in the evaluation, qualification, and monitoring of Gore's sourcing of externally provided components, supplies, and services. You will work in conjunction with development, manufacturing, procurement, raw materials, warehouse, and supplier teams to evaluate and monitor suppliers' quality systems and performance to meet Gore's requirements. This position will be located at our Lovett and Elk Mills 1 facilities in Elkton, Maryland, with the possibility of a hybrid remote work arrangement, depending upon the responsibilities of the role and business needs. Pay and Benefits: $80,000 - $111,000 per year Factors considered in extending an offer within this pay range include (but not limited to) education, experience, knowledge, skills, and abilities. Medical, Dental and Vision benefits effective on Day 1 of employment! We offer a comprehen

Job Description Title: Quality Assurance Specialist Department: Payroll Reports To: Director, Payroll Salary Range: $52,280 - $70,373 Job Summary Participates in the development, implementation and maintenance of quality assurance plans. Conducts quality assurance reviews to ensure that work plans are executed in accordance with the School District of Philadelphia policies and procedures. Studies processes to determine cause and effect. Documents and evaluates data gathered and makes recommendations to the Director, Payroll. Essential Functions Identifies, recommends and implements changes to enhance the effectiveness of quality assurance strategies; assists with the development of quality assurance initiatives . Verifies allocation and calculation of leave days in accordance with District policies. Researches information on current and former School District of Philadelphia employees using the payroll system. Prepares and analyzes basic reports and provides the Director, Payroll with

**Quality Assurance Inspector** **Position Summary:** Catalent is a global, high-growth, private company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. This 206,878 square-foot facility, located in the Philadelphia area is Catalents global Center of Excellence for Clinical Supply Packaging. Catalent offers GMP secondary packaging and clinical labeling services throughout our global network. Packaging can be configured to hold a single product, or multiple products as determined by study requirements. We offer manual patient kit assembly along with semi-automated and automated wallet sealing and high-speed automated carding to meet the needs of studies of all sizes. For temperature sensitive products and those with minimal to zero allowable time out of environment, we can perform secondary packag

Job Description Job Description Education Requirements: B.S. or B.A. in Engineering, Sciences, or related discipline. 2-4 yrs experience (combination of co-op/Real world acceptable). Required Experience and Skills: Strong Technical Writing Skills, Highly developed communication, Leadership and teamwork skills, Ability to manage projects/work to schedule/deadlines. Preferred Experience and Skills: Experience in biologics, vaccine, or bulk sterile manufacturing facilities, Change Control experience, Deviation Management Investigation. Responsibilities: • Authors, supports, updates, and/or leads documentation updates such as SOPs, batch records, change control documents, technical protocols, validation documents and other GMP documentation • Supports deviations, including assessment of product impact and determination of root cause and corrective/preventative actions, assists in writing of investigations as well as quality incidents. • Supports equipment, and facility projects for various

Summary See below for important information regarding this job. Additional vacancies may be filled from this announcement. Responsibilities Perform duties associated with the administration of the quality assurance provisions of contracts by designing, implementing, and maintaining a risk-based surveillance program and assessment plan. Identify opportunities for process improvements through analysis of process measurement data. Serves as a member of a multi-functional or technical team. Responsible for implementing the overall Quality Program for a diversity of products and services in support of U.S. Government acquisition at one or more suppliers facilities. Ensure contractors comply with all requirements related to the design, manufacturing, repair, overhaul, and modernization of a variety of items for contractor and customer activities throughout the world. Independently audit and survey contractors processes to ensure customer and contractual requirements are met. Investigate and