QA Supervisor -- (Frederick,MD)

This job is no longer active. View similar jobs.

POST DATE 9/18/2016
END DATE 10/29/2016

MedImmune, LLC Frederick, MD

Frederick, MD
AJE Ref #
Job Classification
Full Time
Job Type
Company Ref #
Entry Level (0 - 2 years)


b Job Description /b p If you're inspired by the possibilities of science to change lives and you thrive when making brave decisions -- join us. /p p strong MedImmune /strong is the worldwide biologics research and development arm of AstraZeneca. Here, you'll have the opportunity to make a difference in people's lives every day. As one of the world's premier biotechnology companies, our mission is centered on delivering life-changing products that advance world health, and help fight and cure disease. As a strong QA Supervisor in /strong strong Frederick, MD /strong , you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives. /p p We're constantly pushing the boundaries of science to deliver life-changing medicines to patients, with a passion for discovery and a pipeline to show for it. We're pioneering innovative research and exploring novel pathways across key therapeutic areas including oncology, respiratory, inflammation and autoimmunity, cardiovascular and metabolic disease, and infection and vaccines. And we're industry-leading in immunology, protein engineering and translational science. We offer a unique and strong collaborative network as part of the AstraZeneca family, as together we explore synergies between small and large molecules. /p p MedImmune has a dynamic environment that fosters collaboration and innovation. We attract top minds, and we nurture and build top talent. /p h3 Main Duties and Responsibilities /h3 p You will be responsible for ensuring the quality of products manufactured at the facility. Implement scalable solutions, including quality policies, manages quality systems, and facilitates regulatory inspections. Provide leadership and strategy development guidance in areas of regulatory compliance, quality practices and procedures and quality systems to other functional areas. Provide leadership to a staff of Quality Specialists who will report into this position. You will be responsible for the quality oversight of manufacturing operations utilizing efficient batch record review processes and investigations. Document systems, investigation systems and/or change management utilizing a risk based approach. Oversee and manage the Track Wise system for deviations, CAPA, change control, OOS, etc. Ensure that root cause investigations are performed, recommend and/or support implementation of corrective actions to prevent recurrence. Review and approve commissioning, qualification and validation documents (DQ, IQ, OQ, PQ, Steam and Cleaning Validation). Author Standard Operating Procedures, Non-conformances and change controls as required. Work with a cross-functional team of manufacturing, QC, Engineering and Technical Services. Review of documentation associated with incoming receipt and disposition of raw materials used for clinical and commercial manufacturing. Product release utilizing systematic process flows for internal or external customers. Line management and staff supervision includes scheduling, recruiting and performance management. Solid operating skills including timely decisions, managing and measuring work along with good overall timeline and project management skills. You must have the ability to develop staff and set mid and short term priorities. Perform trend analysis to monitor process, systems and facility performance. Create and employ metrics to track the performance of operations and quality systems. Support audits of manufacturing, analytical testing, contractor/supplier and labeling areas to ensure compliance with SOP and regulatory requirements per the requirements of the self-inspection program. Identify areas of potential risk and assists the FMC management team in developing and implementing plans to address them. Alert management to associated liability issues. Provide QA support to QC group by reviewing and approving QC documents (analytical testing, qualification, method validation etc.). /p p  ~BSP /p p /p