Similar Jobs

View More

QA Advisor 9/16/2017

AstraZeneca Pharmaceuticals LP Gaithersburg, MD

Company
AstraZeneca Pharmaceuticals LP
Job Classification
Full Time
Company Ref #
374209
Location
Gaithersburg, MD
Experience
Entry Level (0 - 2 years)
Job Type
Regular
AJE Ref #
579542784

JOB DESCRIPTION

APPLY
b Location: /b Gaithersburg, br Maryland, br United States br b Job reference: /b R-013977 br br b Posted date: /b Sep. 12, 2017 p At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the utmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people’s exceptional skills with those of people from all over the globe. As a b QA Advisor br /b in b Gaithersburg, MD, /b you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. b Operations /b at AstraZeneca is a truly world-class business unit. It offers one of the most exciting, fast paced, challenging and rewarding work environments in the world of operations, supply chain and manufacturing. /p p b Main Duties and Responsibilities /b /p p If you’re inspired by the possibilities of science to change lives and you thrive when making brave decisions – join us. /p p At AstraZeneca, we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. We’re focused on the potential of science to address the unmet needs of patients around the world. We commit to those areas where we think we can really change the course of medicine and bring big new ideas to life. As a Quality Advisor in Development Quality, you’ll have the opportunity to make a difference in people’s lives every day. 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. /p p AstraZeneca is at a critical phase in the journey to deliver our bold ambition; to improve the lives of 200 million patients and be a $50 billion company in 2025. We are on track to deliver 10 new medicines by 2020, and we have one of the most exciting portfolios in the industry. Development Quality is the organisation that provides the quality oversight for Pharmaceutical Technology and Development (PT&D), the bridge that turns brilliant science into actual medicines that help millions of people, and is responsible for ensuring delivery of investigational medicinal products to clinical trials across the globe. /p p As a Quality Advisor, you will report to the Director of Quality Assurance and play a pivotal role in quality support and oversight to GMP operations conducted to deliver AstraZeneca and MedImmune clinical trials. AstraZeneca has a dynamic environment that fosters collaboration and innovation. We attract top minds, and we nurture and build top talent. You will be responsible for review and approval of information provided by internal and external providers, including labelling information, batch and disposition documentation. You will assist client groups in ensuring any deviations and investigations are appropriately investigated and documented and act as Subject Matter Expert supporting internal and external audits and visits to contractor facilities as required. /p p You will support QA management in ensuring the systems and procedures used by AstraZeneca are fit for purpose and appropriately maintained and identify and implement improvements to AstraZeneca’s systems and procedures. You will ensure practices are conducted in compliance with company policies and site procedures. /p p Additionally, you will assist in investigations related to non-conformances, vendor reported deviations, trend analyses, and product complaints using Quality Systems tools such as FMEA and Root Cause Analysis. Upon gaining the relevant experience and knowledge of AstraZeneca systems, you will provide Quality and GMP support to CMC project team(s) and assigned projects. /p