Quality improvement specialist • round rock tx
Coordinate and perform review and approval of completed batch records, raw material records, validations, stability records, and other quality documents to ensure compliance with applicable procedu... Show more
Total Site Solutions, Georgetown, TX, is seeking a detail-oriented Quality Manager.The Quality Manager plays a critical role in ensuring that all products and processes meet or exceed established q... Show more
Quality Assurance Job Duties: Assures consistent quality of production by developing and enforcing g... Show more
Commercial Construction Estimator.Engen Contracting (ECI) | Austin, Texas.At Engen Contracting (ECI), we're looking for more than someone who can prepare estimates—we're looking for a strategic thi... Show more
Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts with national and international companies.We guarantee 15-25 hours per week with an hourly pay of bet... Show more
Manager, Manufacturing Quality.Georgetown, TX Manager, Manufacturing Quality This position is responsible for leading shop-floor quality and driving a prevention-based quality approach within CelLi... Show more
Short term projected expected to last a month.Must provide own PPE (safety glasses, safety vest, steel toe shoes, gloves).We are seeking a detail-oriented and experienced.The ideal candidate will p... Show more
As a Warehouse Quality Control Specialist, you will be responsible for assisting with warehouse operations and ensuring smooth logistics, including: organize inventory and ensure items are stored p... Show more
Contract Review & Negotiation.AI data lab for training frontier models and evaluating AI agents.Experts contribute their diverse subject matter knowledge across domains such as finance, healthc... Show more
Contract Review & Negotiation.AI data lab for training frontier models and evaluating AI agents.Experts contribute their diverse subject matter knowledge across domains such as finance, healthc... Show more
Senior Director, Quality And Supplier Development.Required Skills & Experience: Bachelor's degree in Mechanical, Industrial, or Manufacturing Engineering, or a closely related technical field; adva... Show more
Position Summary TECO-Westinghouse Motor Company is seeking an experienced Quality Engineer II to support the development, application, and maintenance of quality system elements for the manufactur... Show more
Quality Assurance Release Specialist.Reporting to the QA Supervisor, the Quality Assurance Release Specialist is responsible for batch disposition and quality systems oversight to ensure products m... Show more
Contract Review & Negotiation.AI data lab for training frontier models and evaluating AI agents.Experts contribute their diverse subject matter knowledge across domains such as finance, healthc... Show more
Team: Field — Retail Audits & Merchandising.Employment Type: Freelance / Independent Contractor (1099).ThirdChannel matches passionate, lifestyle-driven individuals with the brands they genuine... Show more
Reporting to the QA Supervisor, the Quality Assurance Release Specialist is responsible for batch disposition and quality systems oversight to ensure products meet internal, customer, and regulator... Show more
Contract Review & Negotiation.AI data lab for training frontier models and evaluating AI agents.Experts contribute their diverse subject matter knowledge across domains such as finance, healthc... Show more
Contract Review & Negotiation.AI data lab for training frontier models and evaluating AI agents.Experts contribute their diverse subject matter knowledge across domains such as finance, healthc... Show more
Contract Review & Negotiation.AI data lab for training frontier models and evaluating AI agents.Experts contribute their diverse subject matter knowledge across domains such as finance, healthc... Show more
Aramark Student Nutrition provides food and nutrition services to over 350 school districts in the U.It offers public and private education institutions a variety of dining options including breakf... Show more
The average salary range is between $ 68,764 and $ 71,033 year , with the average salary hovering around $ 70,500 year .
The average salary range is between $ 52,041 and $ 101,598 year , with the average salary hovering around $ 69,678 year .
Coordinate and perform review and approval of completed batch records, raw material records, validations, stability records, and other quality documents to ensure compliance with applicable procedures, test specifications and methods. Perform document record review and approval of batch records, equipment qualifications, calibration records, analytical methods, method validations, stability protocols, and other quality documents for completeness and accuracy. Generating and review Certificate of Analysis (CoA) for catalog and custom projects. Assist in preparation and hosting external audits including customer, ISO, and DEA audits. Generate quarterly metrics summarizing documentation review and production activities. Perform review and approval of Standard Operating Procedures to ensure compliance with regulatory and company quality requirements. Regularly communicate with the QA management any problems and concerns that may delay or lead to the failure of the completion of projects, qualifications, validations, or other quality documents. Assist with internal audits as needed to maintain audit schedule. Support rollout of local and corporate initiatives.
Bachelor's Degree in Chemistry, Biology, or other Life Science Discipline. 5+ years of experience in an ISO environment. Working knowledge of quality system requirements of the pharmaceutical and/or clinical industries. Prior work experience in an ISO, or similarly regulated environment. Knowledge of ISO 9001, ISO 17025, ISO 17034 and ISO 14001. Strong technical knowledge base and the ability to comprehend and communicate basic technical concepts. Ability to communicate effectively with all levels within the organization and with outside contacts. Self-motivated with the ability to work independently. Ability to critically review documents for discrepancies with written procedures and requirements. Knowledge with Root Cause Analysis and experience with eQMS system Veeva or similar.
