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.
Are you ready to take on a role that lets you work independently and self-manage activities with little supervision? As a Quality Control Senior Analyst, you will be responsible for day-to-day job functions, complex administration tasks, and providing support for site initiatives. This is your chance to break new ground and leave a collective legacy in our Operations department!
Accountabilities:
As a QCISO, you will act as a liaison between QC and various groups across the organization. Your wide array of technical expertise will be put to use in maintaining and implementing changes to enterprise systems, supporting commercial product technical transfer, and participating in global IT initiatives. You will also prepare and execute protocols, manage deviations, change controls, and CAPAs related to QC computerized systems, and prepare documentation for presentation to Regulatory Agencies. Your ability to work on complex problems and develop procedures on new assignments will be crucial in this role.
Essential Skills/Experience:
- Bachelor's degree in a Scientific / Biotech / Pharmaceutical field of study
- 2 years of analytical testing experience in the pharmaceutical or biopharmaceutical industry
Desirable Skills/Experience:
- Scientific / Biotech / Pharmaceutical / IT field of study
- 4 years information management experience
At AstraZeneca, we are constantly evolving to stay ahead in rapidly changing markets. Our resilience helps us thrive as we innovate and evolve. We are a diverse, multigenerational team of experts connected across the globe. We interpret the science, connecting it with the business need to apply manufacturing excellence. If you are driven, take smart risks, and are able to act quickly, then AstraZeneca is the place for you. We foster an encouraging, positive environment where ideas are welcomed and rewarded.
Join us in our mission to deliver innovative medicines all the way until they ultimately reach our patients. With an unwavering forward-looking mindset, we are focused on staying ahead in a rapidly changing market. If you enjoy working on a complex variety of activities, then this is the place for you.
Ready to make a big impact? Apply now and contribute to life-changing medicines with AstraZeneca!
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.