QA Assistant Salary at W R Grace & Co.-Conn BETA

Job Description Job Description We are seeking a detail-oriented and motivated Quality Assurance Assistant to join our team. In this role, you will support the QA/QC department in ensuring that our processes, products, and systems meet internal and external quality standards. You’ll play a key part in conducting audits, maintaining documentation, supporting compliance efforts, and contributing to continuous improvement initiatives. Key Responsibilities: Assist in conducting departmental audits and help track deficiencies and corrective actions. Maintain records and documentation to ensure compliance with contracts, policies, and industry standards. Support the creation and execution of QA processes, reports, and training materials. Monitor post-implementation results to ensure issues are resolved and improvements are sustained. Participate in the development and delivery of systems compliance training. Help prepare technical documentation, evaluation reports, and quality summaries. Ass

Responsibilities Review and approve applicable document change orders. Assist management in developing strategic regulatory approaches for new product/business development. Oversee the day-to-day activities related to the quality and safety of the Company’s medical device manufacturing of a commercial stage, human tissue based product. Establish and assist with the implementation of quality systems and system improvements. Qualifications BA or BS in the life sciences or a related degree program 5+ years in a role with extensive quality experience in an FDA-regulated environment, with knowledge of commercial-stage medical devices. Direct experience with tissue-based products is preferred. Experience successfully interfacing with accreditation and regulatory agencies (ISO,FDA), writing responses and other documents required in a regulated environment. Applications without resumes attached will not be considered. *By applying for this position, you agree to receive marketing communication

Job Title: Quality Assurance TechnicianJob Description Monitor plant sanitation and personal hygiene as outlined by Good Manufacturing Practices (GMPs) for food processing facilities in CFR and current company GMP Policies. Assist with internal audits and keep a detailed lab notebook. Perform standardized quality sampling & checks during production; organize collected data into electronic logbooks, databases, and report variances and non-conformities to plant management. (This activity could represent even more than 60 % of the time). Follow all required work instructions, work aids and forms as they pertain to Quality, Environment, Safety and Food Safety. Understand, monitor and act accordingly to support ISO-GFSI compliance, FDA-FSMA regulatory requirements, Food Safety & Quality programs. This individual has the authority & responsibility to stop production should the product be out of specification and/or observed food safety. Follow strict regulatory and safety guidelines. Follow

ABOUT ALBERT USTER IMPORTS Albert Uster Imports, Inc. ("AUI") is a privately held gourmet food company headquartered in the Washington, DC area (Gaithersburg, MD) with warehouse locations in Kansas City, Las Vegas, Miami, Los Angeles, San Francisco, Gurnee and Gaithersburg. AUI falls under the Vestar Capital Partners portfolio with affiliate organization, Roland Foods, LLC. Founded in 1968, the company offers over 1,400 products from around the world. We serve leading hotels, restaurants, casinos, cruise lines, airlines, and manufacturers with innovative, high quality products and solutions to their most demanding culinary challenges. We operate a network of distribution centers across the U.S. and serve select international markets as well. AUI has a national direct selling organization of over 60 sales professionals and a staff of culinary experts (chefs and food scientists) adept at custom product solutions. ABOUT THE ROLE AUI HQ in Gaithersburg is currently hiring a Quality Assuran

Supernus Pharmaceuticals is an award-winning biopharmaceutical company with more than 30 years of experience in developing and commercializing products that treat central nervous system (CNS) diseases. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. We currently have 8 products in the market that are making a real impact on patient outcomes. Job Summary: Responsible for supporting the Company's Quality Assurance and quality management systems by initiating & reviewing documentation, including executed batch records for Commercial products, deviations, and change controls. Essential Duties & Responsibilities: Review of GMP documentation from commercial contract manufacturing organizations (CMO); including line clearances, control of raw materials and equipment cleaning processes. Communicating with external CMOs and internal stakeholders to ensure the timely release of material. Performing review of deviations and change controls from

Summary See below for important information regarding this job. Additional vacancies may be filled from this announcement. Responsibilities Ensure contractor compliance 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 applies a wide range of methods, principles, and practices related to the quality control/assurance fields such as statistical analysis, control and sampling, and quality data analysis and evaluation to determine contractor compliance. Incorporates a thorough and detailed QA knowledge in applying various methods and techniques for investigating, analyzing, and ensuring corrective action on complex quality problems. Develop and implement a surveillance plan which begins with clear objectives supported by a master schedule that includes identification of contractor and sub-contractor production needs. Independently perform audits/su

Job Type Full-time Description Job Summary The Sr. Quality Assurance Associate, Compliance & Vendor Management position ensures compliance with cGMP and internal policies, procedures, and specifications. This position is responsible for the vendor qualification program in accordance with cGMP and related company SOP's, state, federal and local laws as applicable. This person should be knowledgeable of cGMP requirements, FDA regulations ICH guidelines on how to run a vendor management program. The persons are fully responsible for the execution and oversight of the vendor management program for all vendors and service providers of Granules Pharmaceuticals. Principle Accountabilities JOB DESCRIPTION & RESPONSIBILITIES Author and review standard operating procedures. Completion and organization of vendor qualification documentation Ability to redesign the vendor management program. Knowledge and the ability to perform audits of but not limited to contract testing labs, contract packagers,

General information Job Posting Title Quality Assurance Manager Date Wednesday, January 29, 2025 City Annapolis Junction State MD Country United States Working time Full-time Description & Requirements Maximus is seeking a Quality Assurance Manager to provide expertise to a federal client in support of their mission-critical systems in defense of our Homeland. As a Quality Assurance Manager, you will play a crucial role in ensuring the delivery of high-quality technology solutions to our clients. This role requires a strong understanding of the technology landscape, excellent leadership skills, and a passion for delivering exceptional products. This position is on-site, five days a week and requires a secret clearance. Maximus TCS (Technology and Consulting Services) Internal Job Profile Code: TCS207, T3, Band 6 Job-Specific Essential Duties and Responsibilities: Develop and implement quality assurance strategies and methodologies Collaborate with cross-functional teams to define quali