Manager, QA Batch Disposition Position Summary: Work Schedule: Monday – Friday, 8am – 5pm. 100% on-site Catalent is a leading global CDMO partnering with pharma and biotech innovators to accelerate development and delivery of life-changing therapies. Our
AtAstraZeneca Cell Therapy, we are building the capabilities required to deliver complex, personalized therapies through a highly coordinated, patient-centered, and globally scalable supply chain. In cell therapy, every movement matters. The reliable and compliant flow of
Description Company Overview Creating a Healthier World through Accessible Biologics: Kashiv BioSciences, LLC is a fully integrated biopharmaceutical company. Kashiv BioSciences, LLC, in the United States, and its subsidiary, Kashiv BioSciences Private Limited, in India (together
Who YOU are and what YOU can become: Maintains a stockroom(s), receiving dock(s) or tool crib(s) with full responsibility for input, maintenance and accuracy of system(s) based inventory records and/or receiving records, as well as the
We are seeking a Senior Oracle Database Engineer with 10+ years of experience developing, troubleshooting, and supporting enterprise-scale Oracle database applications. This position is primarily focused on hands-on SQL and PL/SQL development, production debugging, script remediation,
Johns Hopkins Carey Business School is hiring a Salesforce Developer III who will manage and maintain development across Careys Salesforce environment (including CRM needs for Executive Education, Partnerships and Experiential Learning) and oversee platform administration. In
Would you like to perform rewarding work while contributing to the success of an established, growing company? Navstar is an award-winning organization that has a proven track record of successfully providing IT services and solutions both
Senior Scientist, QC Analytical About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is located 5 miles from the Baltimore Washington International
Description: This QA Auditing Reviewer role is responsible for thoroughly auditing production records, determining batch disposition (Release, Hold, Reject), and executing those decisions in systems like JDE while ensuring held or rejected batches are properly controlled and stored.
Description At Clinical Associates, we make being healthy easier. We connect our patients to a seamless system of integrated medical care, which includes in-house specialists in areas of practice, from cardiology to podiatry. We also offer
Who Are We? Taking care of our customers, our communities and each other. That’s the Travelers Promise. By honoring this commitment, we have maintained our reputation as one of the best property casualty insurers in the
Senior Specialist QA OTFAbout Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is located 5 miles from the Baltimore Washington International (BWI)
Data Administrator Pay rate: $20.00- $22.00/hr Hours: Location: Columbia, MD Duration: 1 year Summary: The Data Administrator is responsible for maintaining the product release tracking database from receipt of donor until product is shipped. The Data Administrator
Associate Director, Digital & Business Process Strategy The Associate Director, Digital & Business Process Strategy leads the vision, roadmap, and value delivery of digital products that span PAS-X, Tulip (MES), data historians, and LIMS within AstraZenecas
Manager, Sterility Assurance The Manager, Sterility Assurance will be responsible for quality assurance oversight of Aseptic Processing Program, Environmental Monitoring and Microbial Control Policies for Gene Therapy Drug Substance and Drug Product Operations. This individual should
Production Planner The Production Planner will have responsibility for reviewing sales orders, calculating material requirements, creating production schedules, interpreting drawings, incorporating engineering change notices, preparing shipping documents and coordinating project closeouts. Responsible for on-time delivery of
Quality Administrator-Jr The Data Administrator is responsible for maintaining the product release tracking database from receipt of donor until product is shipped. The Data Administrator logs paperwork progress and maintains a 5S file room environment. This role
Quality Management Role at Cardinal Health Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications. Quality Management provides strategic oversight, leadership and direction within the
Senior Specialist, Cell Therapy Trade Compliance Free Trade Zone Operations At AstraZeneca Cell Therapy, we are building the capabilities required to deliver complex, personalized therapies through a highly coordinated, patient-centered, and globally scalable supply chain. In
Senior Scientist, QC Analytical About Site Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is located 5 miles from the Baltimore Washington International