Assembly Worker Salary at Qvc Inc BETA

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

QA Specialist – Malvern, PA Responsibilities: Maintain and improve the site’s Quality Management System. Oversee the site’s compliance with cGMPs, corporate policies, and procedures. Creation and maintenance of controlled documentation, including SOPs, Analytical Data, COAs, Methods of Analysis, etc. Review and approval of change control, deviations, CAPAs, and LIRs. Administrator of site training including scheduling, re-training, and training on revised documentation. Review and approve documentation for the disposition of GMP components, raw materials, intermediates, and APIs. Review and approve master and executed batch records for GMP campaigns. Assist in audits. Qualifications: Bachelor’s of Science Degree with 3-5 years of industry experience Knowledge of regulatory compliance including 21CFR Part 211 Strong organizational skills and detail oriented Strong technical writing skills Ability to work independently to meet tight deadlines. Experience working in a synthetic and/or ana

Quality Specialist Havre De Grace, MD 10-month contract (could go longer) Pay: $25-$37/HR Job Summary: Supports the Quality Manager in maintaining and improving the Quality Management System (QMS). Ensures compliance with ISO-9001, GFSI (Food Safety) certifications, and other regulated industry standards. Oversees Quality Control lab functions and drives process improvements using risk assessment principles Qualifications: • 5+ years of experience in quality, laboratory, or supervisory roles. • A bachelor's degree in Physical Sciences is preferred (relevant experience is considered in lieu of education). • Strong leadership, problem-solving, and communication skills. • Proficiency in Microsoft Office, statistical software (Minitab), SAP, and LIMS preferred. • Experience with ISO 9001, HACCP, GFSI standards, and IPEC GMP requirements. • Lean Six Sigma Green Belt preferred (Black Belt desirable). Key Responsibilities: Quality Management & Compliance: • Maintain an auditable QMS in line w

Job Description Job Description Stylex, Inc., is seeking factory workers in our Delanco NJ location! Stylex, Inc. is a prominent high-end commercial furniture designer and manufacturer located in the greater Philadelphia region. We are experiencing rapid growth and are seeking motivated dedicated individuals to join our team and grow with us. We have second shift positions, advancement opportunities, a team atmosphere centered around employee safety and a competitive benefits package. Positions available: Production Assembly Worker Responsibilities: Work with a team to assemble entire products or components Rotate through tasks for specific production processes Conduct quality inspections on products and parts Prepare finished products for shipment Maintain a clean and orderly work area Basic computer skills necessary for reporting production Qualifications: Previous experience in manufacturing, assembly, or other related fields Familiarity with assembly tools and equipment Ability to

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

Requisition Number - OMF-REQ-0001636 Number of Resources - 1 Start Date - 1/1/2024 End Date - 6/30/2024 Work Location - HQ_Wilmington DE Management Office (1011 Centre Rd Ste 402, Wilmington, DE 19805) Estimated Total Expense Amount Per Resource Requisition - StatusOpen Job Description Type of Service - Corporate/Central Job Title - Originations New Product Quality Assurance Specialist Job Description OneMain Financial is the country's largest lending-exclusive financial company, proudly serving millions of customers with safe, affordable and transparent installment loans. Our customers turn to us every day-online and at over 1,400 branches in 44 states-to help them take control and improve their financial lives . It's all about doing the right thing-a mission that hasn't changed for more than 100 years. "•Provide routine and clerical support for the Income Linked Lending Pilot •Audit payment transaction entries and transmissions - detect and correct errors, managing to a 0% error rate

6-month contract to hire 2nd shift Tuesday-Friday (2:30PM - 12:30AM); 10% shift differential Level I- $38/hr, could potentially level up to level II depending on experience The Specialist I is responsible for day-to-day Quality Assurance Operations activities in accordance with cGMPs, CFRs, ICH guidelines and company policies and procedures. The Specialist I will work onsite alongside manufacturing and quality control personnel, helping to ensure that the highest standard of work is performed. This individual is collaborative, organized, innovative, flexible, with a strong desire to learn and take ownership and accountability. The Specialist I will support Quality Assurance lot release and disposition activities including process observation, batch record review, and completion of lot release documentation. The Specialist I supports Quality Assurance initiatives including, but not limited to, review of laboratory investigations and deviation investigations. The successful candidate wil

Overview: The Quality Assurance Specialist - Testing reviews laboratory testing data/records in accordance with current Good Manufacturing Practices (cGMP), and Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies, as applicable. Monitor processes for adherence to established procedures/regulatory compliance. Provides guidance for quality related issues and consults with QA Management to resolve complex quality issues in a timely manner. Position Details: Schedule: Tuesday to Saturday 10 AM to 6:30 PM Full Time, Benefitted position 100% onsite Responsibilities: Stay current with changes to GXP, including FDA and EU and other regulatory bodies as well as guidance documents (e.g.,: ICH, ISPE, etc.). Maintains awareness of activities by routine direct observation of testing laboratories. Interact frequently with laboratory/operations/facility staff to provide quality perspective on routine operations and support systems. Address conditions/practices with appropriate personne