Job Description
Our Frederick Manufacturing Center (FMC) creates life-changing medicines for people around the world and has been recognized by our local community as being a Top 50’ Business in Frederick and awarded Frederick County’s ‘Best Place to Work’. This distinctive biologic manufacturing facility, with over 800 employees, makes a direct contribution to treating people with cancer, respiratory and autoimmune conditions across the globe. We work hard to deliver life-changing medicines to patients, and we take time to have fun and celebrate our accomplishments. From catered site festivities to competitive events, community outreach activities, environmental and wellness showcases and team-building functions, we take time to recognize our achievements and celebrate our diversity. We are dedicated to creating a culture of inclusion and collaboration and are committed to continuous learning by offering ongoing skill building and training for our staff. Fueled by our aspiration to deliver accelerated growth for our company and to make people’s lives better, there’s never been a more exciting time to join the team and shape the future of AstraZeneca Operations.
As a QC Information Systems (QCIS) Specialist, you will act as an administrator of a variety of GMP computerized systems and serve as a business analyst between lab groups and IT, including Enterprise projects such as Empower, Biovia Laboratory Execution Systems (LES), Labware LIMS, and other digital initiatives. Candidates should have a technical understanding of Information and Enterprise systems. You will be responsible for day-to-day job functions, administration, validation, and data integrity tasks, and can independently represent the team for site and global initiatives.
Accountabilities
1. Perform day-to-day activities and application administration of lab and manufacturing quality control computerized systems, including maintaining static data.
2. Support QC lab functions, providing solutions to a variety of technical problems.
3. Participate in software/computer system validation, IT for software/computer applications and fulfill all networking and security requirements for enterprise software applications.
4. Execute protocols, reports, investigations, and other records using Veeva on behalf of QC.
5. Support QC information system lifecycle management activities from concept, development, validation, implementation, maintenance, to retirement.
Essential Skills/Experience
1. Bachelor’s Degree in science related field.
2. 0-3+ years in systems or lab setting.
Desirable Skills/Experience
1. Degree in Information Systems/Technology or Biotechnology related field.
2. Experience in information management and/or a scientific lab setting.
At AstraZeneca, we take pride in our critical role as the eyes and ears of our patients. We monitor and sign off each batch with the utmost responsibility, ensuring that every contribution we make improves the quality of patients' healthcare and their overall quality of life. Our forward-looking mindset allows us to innovate continuously, trialling the latest models and technologies to enhance reliability and excellence in our processes. Here, you'll feel empowered to make decisions that put patients first while working in an inclusive and friendly community where each voice matters.
Join us in making a real-life difference to patients by applying today!
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