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Associate Scientist I - Quality Control - Madison Wisconsin
Company: Disability Solutions Location: Madison, Wisconsin
Posted On: 01/19/2025
Associate Scientist I - Quality ControlPosition SummaryCatalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. --Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing innovative technologies and solutions to help more and better biologic treatments get to patients. --The business includes our proprietary GPEx cell line engineering platform, our new state-of-the-art biomanufacturing facility in Madison, WI.--Leveraging our growing differentiated technology portfolio, world class manufacturing capability, and other integrated services across the Catalent network, Catalent Biologics is positioned to drive significant growth for Catalent.The Associate Scientist I - Quality Control is an entry level laboratory role with the expectation that the candidate is able to be trained on technical procedures and once trained, execute them consistently and reliably. The Associate Scientist I - Quality Control may support preventative maintenance and basic laboratory maintenance activities while maintaining a GMP quality system.Catalent is committed to a Patient First culture through excellence in quality and--compliance, and to the safety of every patient, consumer, and Catalent employee.--The Role - Executes and properly documents cGMP Quality Control testing with supervision.
- Operates basic cGMP Quality Control equipment. Accurately completes routine and preventive maintenance on basic equipment.
- Performs self-review of analytical data for accuracy and consistency with SOP.
- Enters data into Laboratory Information Management System (LIMS) or laboratory reports.
- Performs solution preparations. Perform facility monitoring of gas and water sampling.
- Perform routine Environmental Monitoring in manufacturing environment: active air sampling, non-viable particulate monitoring, surface and personnel sampling.
- Log in samples into laboratory tracking software.
- Performs general lab housekeeping in adherence to 5S standards.
- Stages materials/components for use within cGMP Quality Control Lab.
- Other duties as assigned.The Candidate
- Bachelor's Degree in Biology, Biotechnology, Chemistry, or related life sciences field, OR Associate Degree in Biology, Biotechnology, Chemistry, or related life sciences field with a minimum of 1 year of industry experience, OR High School Diploma or equivalent with a minimum of 4 years of industry experience.
- Basic understanding of analytical chemistry and simple lab equipment preferred.
- Familiarity with clean room procedure, aseptic technique, and general lab equipment experience.
- cGMP, Good Documentation Practices (GDP), Good Laboratory Practices (GLP) knowledge, and experience following standard operating procedures (SOP) preferred.
- General laboratory equipment experience, including micropipettes.
- Frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening. Occasional stooping, kneeling, crouching, bending, carrying, grasping. Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds. Must comply with EHS responsibilities for the position. Working in a lab environment will require working with skin irritants, lung irritants, electrical equipment, sharp instruments, toxic materials, and hazardous waste. Safety procedures will be followed to minimize exposure, including clean room gowning. Working conditions will be Heating Ventilation and Air Conditioned controlled.Why You Should Join Catalent
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